Abstract
This consensus statement is an update of the 2010 ACSM position stand on exercise and type 2 diabetes. Since then, a substantial amount of research on select topics in exercise in individuals of various ages with type 2 diabetes has been published while diabetes prevalence has continued to expand worldwide. This consensus statement provides a brief summary of the current evidence and extends and updates the prior recommendations. The document has been expanded to include physical activity, a broader, more comprehensive definition of human movement than planned exercise, and reducing sedentary time. Various types of physical activity enhance health and glycemic management in people with type 2 diabetes, including flexibility and balance exercise, and the importance of each recommended type or mode is discussed. In general, the 2018 Physical Activity Guidelines for Americans apply to all individuals with type 2 diabetes, with a few exceptions and modifications. People with type 2 diabetes should engage in physical activity regularly and be encouraged to reduce sedentary time and break up sitting time with frequent activity breaks. Any activities undertaken with acute and chronic health complications related to diabetes may require accommodations to ensure safe and effective participation. Other topics addressed are exercise timing to maximize its glucose-lowering effects and barriers to and inequities in physical activity adoption and maintenance.
Keywords: exercise, physical activity, type 2 diabetes
Synopsis
This consensus statement is an update of the 2010 position stand on exercise and type 2 diabetes (T2D) published jointly by the American College of Sports Medicine (ACSM) and the American Diabetes Association (ADA) (1, 2). In the ensuing decade, a considerable amount of research on select topics in exercise in individuals of varying ages with T2D has been published while diabetes prevalence has continued to expand worldwide. The objective of this consensus statement is to provide readers with a summary of the current evidence and extend and update the prior recommendations from 2010. The writing group used a consensus approach to synthesize available evidence from clinical trials and case reports, narrative and systematic reviews, and meta-analyses, and the recommendations represent the consensus of the writing panel and ACSM and incorporate guidance from other professional organizations with expertise in this area, such as the ADA (1, 2). Current science, new topics for discussion, and clinical experience in making recommendations for participation by people with T2D of all ages are highlighted. In addition, the title of the consensus statement and the text itself have been expanded to include physical activity, a broader, more comprehensive definition of human movement of which structured or planned exercise is a subset.
Introduction
Currently diabetes affects over 463 million people worldwide (3), and its prevalence in the United States is 10.5% (4). T2D accounts for 90-95% of all cases (5). The goal of treatment for T2D is to facilitate an individualized treatment plan, one that may include education, glycemic management, reduction of cardiovascular disease (CVD) risk, and ongoing screening for microvascular complications, in order to achieve and maintain optimal blood glucose, lipid, and blood pressure levels that prevent or delay chronic complications. Lifestyle interventions and/or medications are usually prescribed for treatment of T2D, and more recently, bariatric surgery has also become part of a possible treatment plan.
During any type of physical activity (PA), glucose uptake into active skeletal muscles increases via insulin-independent pathways. Blood glucose levels are maintained by glucoregulatory hormone-derived increases in hepatic glucose production and mobilization of free fatty acids (6, 7), which may be impaired by insulin resistance or diabetes (7). Improvements in systemic, and possibly hepatic, insulin sensitivity following any PA can last from 2 to 72 h, with reductions in blood glucose closely associated with PA duration and intensity (8–10). Additionally, regular PA enhances β-cell function (11), insulin sensitivity (12), vascular function (13, 14), and gut microbiota (15), all of which may lead to better diabetes and health management as well as disease risk reduction.
Impact of Exercise/PA on Diabetes Management and Health Risks
Multiple types of PA enhance health and glycemic management in people with T2D, although structured exercise training has been studied most frequently. Many of the proven benefits result from improved insulin sensitivity, postprandial hyperglycemia, and CVD risk.
Aerobic exercise training
Short-term aerobic exercise training improves insulin sensitivity in adults with T2D, paralleling improved mitochondrial function (16). Vigorous aerobic exercise training for 7 d may improve glycemia without lowering body weight via increased insulin-stimulated glucose disposal and suppression of hepatic glucose production (12). Short-term aerobic exercise in individuals with obesity and T2D improves whole body insulin action through gains in peripheral insulin sensitivity more so than hepatic insulin sensitivity (17). Meta-analyses and systematic reviews have confirmed that regular aerobic exercise training improves glycemia in adults with T2D, with fewer daily hyperglycemic excursions and 0.5-0.7% reductions in hemoglobin A1C (A1C) (18–22). Regular training also improves insulin sensitivity, lipids, blood pressure, other metabolic parameters, and fitness levels, even without weight loss (23, 24).
Resistance exercise training
Resistance exercise training in adults with T2D typically results in 10-15% improvements in strength, bone mineral density, blood pressure, lipid profiles, skeletal muscle mass, and insulin sensitivity (25). Combined with modest weight loss, resistance training may increase lean skeletal muscle mass and reduce A1C three-fold more in older adults with T2D compared to a calorie-restricted, non-exercising group that lost skeletal muscle mass (26). A recent meta-analysis of resistance exercise suggests that high-intensity training is more beneficial than low-to-moderate-intensity training for overall glucose management and attenuation of insulin levels in adults with T2D (27).
Combined exercise training
Interventions with combined aerobic and resistance exercise training may be superior to either mode alone. A greater reduction in A1C has been noted in adults with T2D undertaking a combined training program compared with either type alone (28); however, combined training group participants had a greater exercise volume. In another trial, combined training significantly improved A1C levels over non-exercising controls, although neither resistance nor aerobic training alone resulted in significant changes (29). Moreover, the combined group lost more weight and improved aerobic fitness more so than controls. A meta-analysis (21) showed that all three exercise modalities favorably impact glycemia and insulin sensitivity, and combined training may produce greater reductions in A1C than either training modality alone (30).
High-Intensity Interval Exercise (HIIE).
Higher intensities of aerobic training are generally considered superior to low-intensity training (31). HIIE training is a regimen that involves aerobic training done between 65-90% VO2peak or 75-95% heart rate peak (HRpeak) for 10 sec to 4 min with 12 sec to 5 min of active or passive recovery. HIIE has gained attention as a potentially time-efficient modality that can elicit significant physiological and metabolic adaptations. One session of HIIE (10 × 60 s cycling at ~90% HRmax) reduced postprandial hyperglycemia in adults with T2D (32). Two wks of afternoon HIIE training were shown to improve continuous glucose monitor (CGM)-monitored glycemia while morning training may increase glucose levels on exercise days, particularly if undertaken fasted (33). HIIE training also significantly improves fitness levels and reduces A1C and body mass index (BMI) in adults with T2D. Compared with continuous walking matched for energy expenditure, HIIE training resulted in greater fitness, better body composition, and improved CGM-monitored glycemia (34), as well as enhanced insulin sensitivity and pancreatic β-cell function in adults with T2D (35). Individuals with T2D who seek to improve glycemia with HIIE should closely monitor their responses to training, as chronic intense training may have negative effects such as transient post-exercise hyperglycemia.
The maximal activity of citrate synthase and skeletal muscle mitochondrial protein content in adults with T2D are improved following just 6 sessions of low-volume HIIE (36). Further changes observed with HIIE training include greater reduction in A1C and CVD risk factors with less exercise time (37), as well as enhanced diastolic function (38), increased left ventricular wall mass, greater end-diastolic blood volume due to increased stroke volume and left ventricular ejection fraction (39), and improved endothelial function (40).
Types of Exercise Training Compared.
Glycemia and insulin sensitivity in adults with overweight/obesity and with insulin resistance, prediabetes, or T2D are improved similarly with different modes of structured exercise training when energy expenditure is matched (41–44). Adverse events have been reported in 34% of studies included in a meta-analysis, with a majority attributable to musculoskeletal injuries during HIIE rather than moderate training (45). The benefits of other types of PA are less well established and have mixed glycemic outcomes. Yoga may improve A1C, blood lipids, and body composition in adults with T2D (46); whereas, tai chi may improve glycemic management, balance, neuropathic symptoms, and some dimensions of quality of life (47). Further studies are required to fully establish the potential benefits of yoga and tai chi in populations with T2D.
Exercise/PA with and without Weight Loss
Dietary restriction and increased PA are the cornerstones of intensive lifestyle (ILS) interventions that are typically used to induce weight loss. Such interventions may prevent or delay onset of T2D in at-risk populations and reduce CVD risk in individuals with T2D. In many cases PA has been shown to be as important as, if not more so than, weight loss.
T2D Prevention.
The U.S. Diabetes Prevention Program (DPP) multicenter trial utilized ILS with a goal of achieving modest (5-7%) weight loss and led to the important observation that for every 1 kg of body weight lost, T2D risk was reduced by 16% (48). Even among those failing to meet the weight loss goal of 7% during the first year, individuals meeting the PA goal had a 44% reduction in diabetes incidence, independent of the small weight loss (−2.9 kg) (48). The DPP outcomes study (DPPOS) has shown a higher incidence of T2D onset in those who gained weight at 10 and 15 years after participating in the original ILS arm (49, 50). More recent follow-up data from DPPOS shows that cumulative T2D incidence remained lower in the ILS group, a finding not explained by differences in body weight among groups (51); rather, PA was inversely related to incident of T2D for all participants. Importantly prevention of T2D was enhanced in active participants with lower baseline PA, and moderate-intensity walking (about 18.2 km/wk) improved oral glucose tolerance with only 2 kg of weight loss (52). Overall, individuals at high risk for developing T2D who have initially low PA levels benefit the most from moderate-intensity walking and other exercise with minimal weight loss.
CVD Risk Reduction.
Most ILS interventions in adults with T2D have also led to a reduction in CVD risk factors. In the Look AHEAD trial (53), ILS participants with T2D lowered triglycerides and increased HDL-C levels. More weight loss led to greater improvements in A1C, systolic blood pressure, HDL-C, and triglyceride levels. Most ILS trials (focused primarily on dietary changes and increased PA) with weight reduction as a goal in adults with T2D have resulted in <5% weight loss and few beneficial metabolic outcomes (54, 55). A weight loss of >5% appears to be necessary for beneficial effects on A1C, blood lipids, and blood pressure in most individuals (54, 55). During the first year of the trial, ILS participants experienced greater reductions in A1C, initial improvements in fitness and attenuation of all CVD risk factors except for LDL-C levels. Further, ILS did not reduce the occurrence of a composite CVD outcome score over 9.6 y despite the greater, sustained weight loss in participants (56), but the participants had fewer hospitalizations, medications, and health care costs over 10 y (57). Thus, lifestyle interventions that include PA in recommended amounts and possible weight loss remain important approaches in the management of T2D and CVD risks.
Weight Loss and Regional Fat Distribution.
Weight loss from PA alone is generally small, although possible with 1 or more hours of daily moderate-or high-intensity exercise (58–60). In men and women with obesity, 1 h of daily moderate-intensity aerobic exercise induced weight loss similar to dietary restrictions alone, with similar reductions in abdominal subcutaneous and visceral fat observed in both groups. Regular exercise without weight loss also reduced subcutaneous and visceral fat and prevented further weight gain (58). In postmenopausal women with T2D, modest weight loss with either dietary restriction alone or diet plus exercise similarly reduced total abdominal fat, subcutaneous adipose tissue, and glycemia, but the addition of exercise was necessary for visceral adipose tissue loss (61), which leads to lesser metabolic dysfunction and CVD risk. Thus, moderate-to high-intensity exercise (~500 kcal) done 4-5 d/wk appears to reduce abdominal, but particularly visceral, fat in adults with T2D and may lower their metabolic risk.
Prevention of Gestational Diabetes.
Women with gestational diabetes mellitus (GDM) may have a nearly 10-fold higher risk of developing T2D at some point (62). PA is a preventative tool for GDM and subsequent development of T2D (63, 64). Prepregnancy exercise training has been consistently associated with a reduced risk of GDM (65–68). Moderate aerobic exercise performed 3 d/wk (50-55 min/session) for 8-10 wk through the third trimester reduces the prevalence of GDM (2.6% vs. 6.8% with standard care) and minimizes excessive weight gain during pregnancy (69). Cycling exercise (30 min, 3x/wk) initiated early in pregnancy has been shown to reduce the frequency of GDM in women with overweight/obesity and lowered gestational weight gain before the mid-second trimester (70). A recent meta-analysis concluded that prenatal exercise alone, including 140 min of moderate-intensity exercise weekly, results in a 25% reduction in risk of GDM, preeclampsia, and gestational hypertension (71). Regular PA of any type during pregnancy decreases the incidence of GDM and maternal weight gain without serious adverse events (72). It is widely recommended that pregnant women participate in ~20-30 min of moderate-intensity aerobic exercise most days of the week, but the total amount of PA needed to achieve these diabetes risk reductions may be greater (73, 74).
Mental Health and Cognition Benefits of PA
Regular PA potentially has psychological and cognitive function benefits for people with T2D. Both are important for the long-term health of this population.
Mental Health.
Participation in both short-and long-term exercise training has been shown to substantially decrease symptoms of depression and anxiety in individuals across all age groups diagnosed with clinical depression (75). Exercise increases certain brain hormones that modulate hippocampal plasticity to improve both cognition and mental health (76). In the Look AHEAD trial, participants following ILS had improved health-related quality of life and reduced symptoms of depression after 12 m (77), and the benefit extended as long as 8 y (78). In the U-TURN study (79), participants with T2D who undertook ILS experienced improvements in the physical component of quality-of-life scores but with no change in the mental component at 1 y. Collectively, these studies suggest that regular exercise may improve psychological well-being, including health-related quality of life and depressive symptoms, in individuals with T2D.
Memory and Cognitive Function.
T2D is associated with cognitive dysfunction, including poor attention and concentration, visual and verbal memory, processing speed, and executive function (80). Young and older adults have experienced increases in basal glucose uptake in brain regions critical to cognitive function following 12 wk of aerobic interval exercise (4 × 4 min >90% VO2peak for 3 d/wk) combined with moderate-intensity treadmill walking (70% VO2peak for 2d/wk) (81). Similarly, 2 wk of sprint interval training lowered insulin-stimulated glucose uptake in the temporal cortex, cingulate gyrus, cerebellum as well as global regions when compared with other moderate-intensity continuous exercise training in sedentary, middle-aged adults with insulin resistance (82). When PA is combined with a low-fat diet, brain insulin sensitivity is increased in adults with obesity (83). Surprisingly, there is a paucity of research on the effects of exercise on memory and cognitive function in people with T2D (84–87). Although the Look AHEAD trial reported no cognitive benefit after 8-9 y of lifestyle treatment in people with T2D (88), a recent meta-analysis suggested a favorable, albeit small to moderate, effect of exercise on executive function and memory (89), similar to reported associations between exercise and cognitive function in adults with T2D (90, 91). There is a paucity of data on the physiological mechanisms related to memory, cognitive function, and cerebral blood flow.
PA Recommendations for Individuals with T2D
The 2018 update of the Physical Activity Guidelines for Americans (Table 1) included recommendations for youth, adults, and older adults (92, 93). In general, these recommendations apply to individuals with T2D as well, with a few exceptions and modifications (Table 2). In most instances, the recommendations for adults of all ages are the same unless comorbid health conditions or older age impact their ability to be active and modifications are needed (92).
Table 1:
Adults | Move more and sit less throughout the day. Some physical activity is better than none. |
For substantial health benefits, do at least 150 min (2 h, 30 min) to 300 min (5 h) a week of moderate-intensity, or 75 min (1 h, 15 min) to 150 min (2 h, 30 min) a week of vigorous-intensity aerobic physical activity, or an equivalent combination of moderate- and vigorous-intensity aerobic activity, preferably spread throughout the week. | |
Additional health benefits are gained by engaging beyond the equivalent of 300 min (5 h) of moderate-intensity physical activity weekly. | |
Perform muscle-strengthening activities of moderate or greater intensity and that involve all major muscle groups on 2 or more days/week. | |
Older Adults | The guidelines for healthy older adults are the same as those for all adults. |
In addition, as part of weekly physical activity, do multicomponent physical activity that includes balance training as well as aerobic and muscle-strengthening activities. | |
Determine level of effort for physical activity relative to the level of fitness. | |
With chronic conditions, understand whether and how the conditions affect the ability to do regular physical activity safely. | |
If an individual cannot do 150 min of moderate-intensity aerobic activity a week because of chronic conditions, engage in as much physical activity as abilities and conditions allow. | |
Children and Adolescents | Preschool-aged children (ages 3 through 5 y) should be physically active throughout the day to enhance growth and development. |
Adult caregivers of preschool-aged children should encourage active play that includes a variety of activity types. | |
Provide young people opportunities and encouragement to participate in physical activity appropriate for their age, that are enjoyable, and that offer variety. | |
Children and adolescents ages 6 through 17
years should engage in 60 min (1 h) or more of moderate-to-vigorous
physical activity daily: • Aerobic: Most of the 60 min or more per day should be either moderate-or vigorous-intensity aerobic physical activity and should include vigorous-intensity physical activity on at least 3 d/wk. • Muscle-strengthening: As part of 60 min or more of daily physical activity, include muscle-strengthening activities on at least 3 d/wk. • Bone-strengthening: As part of 60 min or more of daily physical activity, include weight-bearing exercise to strengthen bones at least 3 d/wk. |
Table 2.
Type of Training | Type | Intensity | Frequency | Duration | Progression |
---|---|---|---|---|---|
Aerobic | Walking, jogging, cycling, swimming, aquatic activities, rowing, dancing, interval training | 40%-59% of VO2R or HRR (moderate), RPE 11-12; or 60%-89% of VO2R or HRR (vigorous), RPE 14-17 | 3-7 d/wk, with no more than 2 consecutive days between bouts of activity | Minimum of 150 to 300 min/wk of moderate activity or 75 to 150 min of vigorous activity, or an equivalent combination thereof | Rate of progression depends on baseline fitness, age, weight, health status, and individual goals; gradual progression of both intensity and volume is recommended |
Resistance | Free weights, machines, elastic bands, or body weight as resistance; undertake 8-10 exercises involving the major muscle groups | Moderate at 50%-69% of 1-RM, or vigorous at 70%-85% of 1-RM | 2-3 d/wk, but never on consecutive days | 10-15 repetitions per set, 1-3 sets per type of specific exercise | As tolerated; increase resistance first, followed by a greater number of sets, and then increased training frequency |
Flexibility | Static, dynamic, or PNF stretching; balance exercises; yoga and tai chi increase range of motion | Stretch to the point of tightness or slight discomfort | ≥2-3 d/wk or more; usually done with when muscles and joints are warmed up | 10-30 s per stretch (static or dynamic)group; 2-4 repetitions of each | As tolerated; may increase range of stretch as long as not painful |
Balance | Balance exercises: lower body and core resistance exercises, yoga, and tai chi also improve balance | No set intensity | ≥2-3 d/wk or more | No set duration | As tolerated; balance training should be done carefully to minimize the risk of falls |
Note: VO2R, VO2 reserve; HRR, heart rate reserve; 1-RM, 1-repetition maximum; RPE, rating of perceived exertion; PNF, proprioceptive neuromotor facilitation.
Adults and Older Adults
Aerobic Exercise.
All adults with T2D should follow the same recommendations, with no more than two consecutive days between bouts due to the transient nature of exercise-induced improvements in insulin action (94, 95). Adults with comorbid health conditions and compromised older adults with T2D should aim to get as much aerobic activity as their physical and mental health allows.
Resistance Exercise.
Resistance exercise training in older adults with T2D results in 10-15% improvement in strength, bone mineral density, lean mass, blood pressure, blood lipids, and insulin sensitivity (25, 96), along with 3-fold greater reductions in A1C (26). Notably, interventions that combine aerobic and resistance training may be superior to either one alone (21, 29, 30). Adults unable to meet current recommendations should focus on improving on functional fitness and balance.
Flexibility Exercise.
Exercises that enhance joint flexibility are highly beneficial for health and well-being in older adults with T2D. Limitations to joint mobility, resulting in part from glycation occurring with normal aging, may be accelerated by hyperglycemia (97). While stretching exercises increase range of motion and flexibility (98), they generally do not impact glycemia unless undertaken as part of another PA such as yoga (99). Flexibility exercises, alone or in combination with resistance training, has been shown to improve joint range-of-motion in individuals with T2D and facilitates participation in activities that require flexibility (98). Moreover, flexibility training is generally low-intensity and easier to perform, thereby providing one possible entry into a more physically active lifestyle for less fit and older adults (1).
Balance Exercise.
Many lower body and core resistance exercises double as balance training (100). Power training undertaken by adults with T2D can improve overall body balance (101). Balance exercises may reduce the risk of falls by improving balance and gait, even in adults with peripheral neuropathy (102, 103). At-home balance exercises may reduce risk of falls even without significant changes in leg strength in older adults with T2D at increased risk for falls (103).
Other Types of Exercise and PA.
Along with traditional static and dynamic stretching, yoga, tai chi, and other types of PA may also provide health and glycemic benefits. Inclusive of basic stretching and strengthening activities, yoga may improve overall glycemia, lipid levels, and body composition in adults with T2D (46, 99, 104, 105). Tai chi training incorporates some balance, stretching, and resistance elements and may improve glycemia, reduce BMI and neuropathic symptoms, and increase balance and quality of life in adults with T2D and neuropathy (106, 107). Various forms of qigong may improve A1C levels and other health and fitness parameters including balance (106, 108, 109). Pilates may improve blood glucose management, along with functional capacity, in older adults with T2D (110). Thus, many alternate types of exercise and PA may be appropriate and beneficial for adults with T2D, especially individuals with lower initial fitness and poorer balance.
Sedentary Time and Activity Breaks.
Physical inactivity (i.e., sitting or lying while awake) increases the risk of T2D across all racial and ethnic groups (111). In sedentary adults with 9 h of sedentary behavior per day, 1 h extra of sedentary time daily over an 8-d period is associated with a 22% increase in the odds of developing T2D (112). Furthermore, greater sedentary time is related to hyperglycemia independent of aerobic fitness (113), although high levels of fitness can attenuate CVD risk factor clustering (114).
In adults with T2D, the interruption of prolonged sitting with activity breaks, such as light-intensity walking or simple resistance activities for 3 min every 30 min over 8 h, decreases postprandial glucose, insulin, C-peptide, and triglyceride levels (115). Replacing sitting time with standing (2.5 h/d) and light-intensity walking (totaling 2.2 h/d) every 30 min may improve 24-h glucose levels and insulin sensitivity more than structured exercise (116). Bouts of stair climbing also have been effective at reducing postprandial glycemia (117, 118), but not necessarily A1C (119). Short 5-min breaks every h over 12 h more effectively lowered glucose and insulin levels than 1 h of moderate-intensity continuous exercise at the beginning of the day in people with impaired glucose tolerance (120), and short bouts of exercise (HIIE consisting of 6 × 1 min walking at 90% max HR) 30 min before meals reduces glucose levels more than a single 30-min bout of moderate walking (121). Small “doses” of PA to break up sitting moderately attenuate postprandial glucose and insulin levels, somewhat more than moderate continuous exercise, with greater effects in people with insulin resistance and a higher BMI (122). However, breaks from sitting have not been shown to lower hyperglycemia in free-living environments (123). Whether long-term use of breaks in sedentary time has clinically relevant glycemic benefits remains unclear.
Adolescents and Youth
PA goals recommended for youth and adolescents with T2D are the same as for youth in the general population (92, 93). Childhood obesity and T2D occur in complex psychosocial and cultural environments making successful implementation of lifestyle interventions difficult (124). Youth with T2D manifest both insulin resistance and non-autoimmune β-cell failure similar to adults; however, youth-onset is associated with a more rapid decline in β-cell function and acceleration of diabetes complications. The Bright Bodies Weight Management Program for Children, a year-long 2x/wk exercise and nutrition/behavior modification program in youth with obesity without diabetes, reduced insulin resistance and T2D risk (125). In a multicenter study in youth with T2D (the TODAY Study), metformin therapy managed glycemia in half of participants, and the addition of rosiglitazone, but not lifestyle changes including PA, was superior to metformin alone (126, 127). A 12-wk gym-based, supervised program in adolescents with T2D improved endothelial function and health, independent of changes in insulin sensitivity (14). Thus, home-based and gym-based exercise and weight management programs should be encouraged for youth with T2D to enhance insulin sensitivity and cardiometabolic function and manage overweight and obesity.
Pre-exercise Evaluation and Testing
For most individuals planning to participate in a low- to moderate-intensity PA like brisk walking, no pre-exercise medical evaluation is needed unless symptoms of CVD or microvascular complications are present (1, 96). In adults who are currently sedentary, medical clearance is recommended prior to participation in moderate-to high-intensity PA. Although suggested by practice guidelines (Table 3), pre-exercise stress testing in asymptomatic adults with T2D remains controversial. One study reported that all participants with T2D had lower rates of major CVD outcomes (< 1%), with no differences between those who underwent stress testing (sedentary with 1 or more cardiac risk factors) and those who did not over 3.4 y, and pre-exercise stress testing did not reduce CVD events (128). In the Look AHEAD trial, only older age was associated with increased prevalence of all abnormalities during maximal exercise stress testing (129), and in the DIAD trial, more intensive testing did not alter event rates (130). Moreover, no evidence is available to determine whether pre-exercise evaluation involving stress testing is necessary or beneficial before participation in anaerobic or resistance training. Coronary ischemia is less likely to occur during resistance compared with aerobic exercise eliciting the same heart rate, and some doubt exists that resistance exercise induces ischemia (131–133).
Table 3:
In general, maximal graded exercise stress testing may be indicated for adults matching one or more of these criteria: |
• Age > 40 y, with or without cardiovascular disease risk factors other than diabetes |
• Age > 30 y
and ○ Type 1 or type 2 diabetes >10 y duration ○ Hypertension ○ Cigarette smoking ○ Dyslipidemia ○ Proliferative or preproliferative retinopathy ○ Nephropathy including microalbuminuria |
• Any of the following,
regardless of age ○ Known of suspected cardiovascular, coronary artery, or peripheral artery disease ○Autonomic neuropathy ○ Advanced nephropathy with renal failure |
Management of Acute and Chronic Health Complications with PA
Numerous acute and chronic health issues may arise around PA initiated by individuals with T2D. Of primary concern are exercise-related hypoglycemia and hyperglycemia. In addition, exercising with chronic health complications related to diabetes may require accommodations to ensure safe and effective PA participation.
Hypoglycemia.
Individuals managing glycemia with lifestyle improvement alone have minimal risk for hypoglycemia (134). Use of select medications for T2D may increase the risk of exercise-related hypoglycemia, including insulin and insulin secretagogues (i.e., sulfonylureas and meglitinides) (7, 135–137). For example, pre-exercise insulin administration increases the risk of hypoglycemia during exercise, and both insulin dosing and timing must be considered. Carbohydrates may be needed if pre-exercise blood glucose levels are likely to lead to hypoglycemia during or following activities and medication doses are not lowered to compensate. No medication dose adjustments or carbohydrate intake is necessary for other oral diabetes medications or non-insulin injectables, such as GLP-1 agonists (96). Later-onset hypoglycemia is a greater concern when carbohydrate stores (i.e., skeletal muscle and liver glycogen) are depleted, but usually is not an issue for most recreational exercisers who are non-insulin users. While high-intensity exercise may be problematic for those taking insulin, finishing an exercise session with a short, high-intensity bout has been shown to be beneficial in preventing hypoglycemia in those not on insulin. Longer duration, high-intensity PA increases the risk for post-exercise hypoglycemia with use of insulin or its secretagogues (138).
Hyperglycemia.
Clinical consensus recommendations state that if blood glucose is >300 mg/dL−1 (16.7 mmol/L−1), caution should be advised when exercising without or with minimal levels of blood or urinary ketones, but ketones are seldom measured or excessively elevated in individuals with T2D. Regardless, if blood glucose is elevated, individuals are advised to only begin light activity if they are asymptomatic and properly hydrated (96, 139). Activities that are short and intense (such as HIIE) may cause a transient increase in blood glucose that remains elevated afterward for a period of time (140, 141). Extra insulin (in users) and/or a lower intensity cool-down following intense activities may be used to reduce post-exercise glucose elevations, although no treatment is needed in most cases (140). Importantly, diabetic ketoacidosis, which normally is the result of hyperglycemia and elevated ketones, may occur with euglycemia or only moderate hyperglycemia in adults with T2D taking oral SGLT-2 inhibitors to manage blood glucose (142). Given these potential confounders, PA should only be undertaken when individuals with elevated blood glucose, even without overt ketosis, are feeling well.
Heat Stress.
Aging alone negatively affects heat loss in both dry and humid environments (143), but T2D also appears to increase the risk of heat stress during PA, but not during passive rest (144). Impairments in whole-body heat loss are related to abnormal cutaneous vasodilation and decreased sweating (145), which can lead to increases in body temperature and heart rate. Consequently, many adults with T2D have a reduced ability to do PA, especially in warm environments, due to an impaired ability to thermoregulate, and with dehydration, their risk of chronic hyperglycemia increases (146). Moreover, certain diabetes-related comorbidities and medications may increase the risk of heat-related illness (147). Heat acclimation has been shown to be possible in adults with T2D engaging in aerobic or resistance training, though, with some improvements in exercise-generated heat dissipation and other factors after adaptation (148, 149). Nevertheless, individuals with T2D should be cautious when exercising in hot environments, although they may acclimatize to hotter conditions with regular PA.
Chronic Health Complications.
Recurrent hyperglycemia increases the risk for chronic complications of diabetes, including macrovascular complications (CVD, PVD and lower limb amputations) and microvascular complications (e.g. retinopathy, nephropathy, and peripheral and autonomic neuropathy (150–152). Prolonged daily sedentary time also increases the risk of T2D, CVD, and premature mortality, even when adjusted for PA levels (153, 154). Most individuals can engage in various types of PA safely and effectively despite having health complications. With regular training, they can anticipate significant and meaningful improvements when following general exercise training precautions (Table 4). Certain activities may be contraindicated due to existing health conditions, and special testing or pre-exercise preparation may be required (Table 5). In individuals with macrovascular diseases or cardiac autonomic neuropathy, pre-exercise screening should follow the guidelines set by ACSM (155) and ADA (96).
Table 4:
Medical clearance (and exercise testing) prior to starting activities more vigorous than brisk walking is recommended for adults with signs or symptoms of cardiovascular disease, longer diabetes duration, older age, or other diabetes-related complications (95). |
Individuals should not begin exercise with a blood glucose >250 mg · dL−1 (13.9 mmol · L−1) if moderate or high levels of blood or urinary ketones are present. Use caution during PA with a blood glucose >300 mg · dL−1 (16.7 mmol · L-1) without excessive ketones, stay hydrated, and only begin if feeling well (95, 139). |
Individuals are advised to hydrate properly by drinking adequate fluids before, during, and after exercise, as well as avoid exercising during the peak heat of the day or in direct sunlight to prevent overheating. |
Particularly for anyone using insulin or taking sulfonylureas (and possibly meglitinides within 2-3 h of physical activity), it is important to carry rapid-acting carbohydrate sources during PA to treat hypoglycemia and have glucagon available to treat severe hypoglycemia (if prone to developing it). |
Table 5.
Health Complication | Precaution |
---|---|
Autonomic Neuropathy | • Be aware of an increased
likelihood of hypoglycemia, abnormal blood pressure responses, and
impaired thermoregulation, as well as elevated resting and blunted
maximal heart rate. • Use of ratings of perceived exertion (RPE) is suggested to monitor exercise intensity. • Take steps to prevent dehydration and hyperthermia or hypothermia. |
Peripheral Neuropathy | • Limit exercise participation
that may cause foot trauma, such as prolonged hiking, jogging, or
walking on uneven surfaces. • Non-weight-bearing exercises (e.g., cycling, chair exercises, swimming) may be more appropriate, but avoid aquatic exercise with unhealed plantar surface ulcers. • Check feet daily for signs of trauma and redness. • Choose shoes and socks carefully for proper fit and wear socks that keep feet dry. • Avoid activities requiring excessive balance ability. |
Diabetic Retinopathy | • With unstable proliferative
and severe retinopathy, avoid vigorous, high-intensity activities that
involve breath holding (e.g., weight lifting and isometrics) or overhead
lifting. • Avoid activities that lower the head (e.g., yoga, gymnastics) or that jar the head. • In the absence of a stress test measured maximal heart rate, use RPE to monitor exercise intensity (10 to 12 on a 6-20 scale). • Exercise is contraindicated for anyone with unstable or untreated proliferative retinopathy, recent panretinal photocoagulation, or other recent surgical eye treatment. • Consult an ophthalmologist for specific restrictions and limitations. |
Diabetic Kidney Disease | • Avoid exercise that causes
excessive increases in blood pressure (e.g., weight lifting,
high-intensity aerobic exercise) and refrain from breath holding during
activities. • High blood pressure is common, and lower intensity exercise may be necessary to manage blood pressure responses and fatigue. • Light to moderate exercise is possible during dialysis treatments if electrolytes are managed. |
Hypertension | • Avoid heavy weight lifting or
breath holding. • Perform dynamic exercises using large muscle groups, such as walking and cycling at a low to moderate intensity. • Follow blood pressure guidelines for activity levels. • In the absence of a measured maximal heart rate, use of RPE is recommended (10 to 12 on a 6-20 scale). |
Exercise Timing and Dietary Considerations
Some studies have addressed optimal timing of exercise around meals and in general to maximize blood glucose management and other health benefits in T2D. In addition, while dietary eating patterns may be used to enhance blood glucose management, their impact on exercise remains equivocal.
Exercise timing
Most acute exercise studies have examined effects on glycemia around breakfast, demonstrating better management with light-or moderate-intensity aerobic exercise undertaken postprandially in individuals with T2D (156–158), but this glycemic benefit does not necessarily carry over to lunch (156, 157). Only one study found better glycemic management with exercise prior to breakfast (159). A comparison of 2 wks of morning or afternoon HIIE (3x/wk) training in men with T2D showed that afternoon sessions reduced blood glucose more than morning sessions, which actually increased glycemia (33). A 12-wk multimodal exercise training program found that either morning and afternoon sessions in men and women with T2D improved A1C, fasting glucose, and HOMA2-IR but not fructosamine, and postprandial glucose and insulin levels were similarly lowered following a mixed meal (160). When exercise was undertaken around dinner, better blood glucose responses occurred with self-selected-pace walking post-meal (161), and blood glucose and triglyceride levels were attenuated by post-meal resistance exercise (162). Overall, most studies have shown that postprandial exercise provides better glucose control by attenuating acute glycemic spikes, and greater energy expenditure postprandially reduces glycemia regardless of exercise intensity or type, with a longer duration (≥45 min) providing the most consistent benefits (61).
Dietary Intake and eating patterns
Prevention or delay of T2D can be achieved with regular PA and maintenance of a healthy body weight, and individuals with T2D should focus on sustainable eating plans that consider the amount and timing of carbohydrate intake in combination with an active lifestyle to manage glycemia, insulin sensitivity, body weight, and CVD risk. According to the 2020-2025 US Dietary Guidelines for Americans (163), a healthy eating plan provides appropriate daily calories; highlights fruits, vegetables, and whole grains; includes reduced or non-fat dairy products, lean meats, poultry, fish, beans, eggs, and nuts; and is low in saturated and trans fats, cholesterol, salt, and added sugar. Whole foods-based eating is micronutrient dense, antioxidant rich, and beneficial in preventing and managing T2D (164). Carbohydrate restriction reduces body weight and improves glycemia (165–168), and use of popular diet options (i.e., low carbohydrate, ketogenic diet) and other eating patterns (i.e., Mediterranean, vegan) are frequently followed for T2D management (169, 170). Time-restricted feeding and intermittent fasting which have multiple definitions have become popular in recent years, but there are limited studies to date in individuals with T2D and the benefits to glycemic management are unknown. Caution is recommended when implementing a ketogenic diet that chronically restricts carbohydrate to ≤50 g/d to induce ketosis (170) as insufficient trials in individuals with T2D support this approach (165, 169, 170) and its impact on PA participation and exercise performance remains equivocal (167, 168, 171–173).
Medical Interventions and Exercise Effectiveness
Anti-diabetes medications are often co-prescribed with exercise for management of T2D. Some of these, as well as others taken for comorbid conditions, may impact the effectiveness of exercise participation. In addition, adults undergoing bariatric surgery to manage obesity and T2D may also be impacted by pre- and post-surgery exercise participation.
Diabetes Medications.
Somewhat surprisingly, pilot studies on adults with insulin resistance have found that metformin, the most commonly prescribed medication for pre-diabetes and diabetes, may attenuate exercise-enhanced peripheral insulin sensitivity benefits following acute (174) and chronic exercise (175) training. In adults with T2D, the normal reduction in postprandial glycemia with metformin use also may be somewhat attenuated by exercise (176). Although it augments skeletal muscle glucose uptake during any PA (177) and improves glycemia in individuals with T2D (178), metformin has been found to potentially blunt AMP-activated protein kinase activity (174) and mitochondrial adaptations to aerobic exercise (179) and attenuate skeletal muscle hypertrophy after weight lifting (180) in healthy adults. Thus, metformin may be contributing to the inter-individual variability observed in exercise-induced improvements in insulin sensitivity and cardiometabolic health (181), but more research is needed in this area.
As for other medications, both GLP-1 agonists and SGLT-2 inhibitors have glucose-lowering mechanisms and downstream metabolic impacts that may impact exercise-induced adaptations. GLP-1 agonists may improve A1C levels and fasting glycemia following aerobic exercise training in adults with T2D, but these findings have been confounded by significant weight loss (182). More research is needed on the interaction of all these medications and exercise. Insulin therapy is often a last option in T2D, but in men with T2D, similar reductions in time spent in hyperglycemia and reduced glycemic variations over 24 h were observed following a 45-60 min bout of exercise with and without insulin use (183). Individuals with T2D using insulin or insulin secretagogues are advised to supplement with carbohydrate (or reduce insulin, if possible) as needed to prevent hypoglycemia before and/or after exercise.
Non-Diabetes Medications.
β-blockers blunt the heart rate responses to exercise and lower maximal aerobic exercise capacity to ~87% of expected via negative inotropic and chronotropic effects (184). While their use may increase risk of hypoglycemia unawareness with PA by blunting adrenergic responses, β-blockers can increase exercise capacity in people with T2D and CVD by reducing ischemia during PA (185). In adults using β-blockers, ratings of perceived exertion (RPE) should be utilized to monitor exercise intensity rather than heart rate (186). In a small number of individuals, statin use has been associated with an elevated risk of myopathies (myalgia and myositis), particularly when combined with fibrates and niacin and hyperglycemia (187).
Bariatric Surgery.
Bariatric surgery is now considered the most effective way to improve glycemic management and achieve diabetes remission over the long term (188, 189); however, less than 10% of adults undergoing bariatric procedures meet PA recommendations pre-surgery, despite the nearly 40% of adults saying they feel ready to exercise 14 d before surgery (190). Preoperative exercise may benefit these individuals by lowering surgical risk and enhancing recovery, as well as reducing the length of hospital stays (191). Increases in VO2peak are also associated with reduced operating time and improved quality of life despite no additional effect on blood glucose levels or insulin sensitivity (192, 193). Others have suggested increased exercise pre-surgery increases the propensity for being active afterward (194). Aerobic exercise training following surgery may further enhance weight maintenance, glycemic management, and insulin sensitivity (195–197), lower risk of CVD, enhance endothelial function (198), and improve cardiac autonomic regulation (199). Resistance exercise training may reverse muscle strength deficits frequently observed after bariatric surgery (200). Exercise training is also effective in ameliorating surgery-related bone loss (201, 202), which is common following bariatric surgery (203–205).
Barriers to Adoption of PA and Inequities
Barriers to PA participation are similar among people with and without diabetes and include lower self-efficacy (206), inappropriate goal-setting (207), lack of access to facilities (208), lack of supervision or social support (209–211), and inattention to cultural nuances (212). Health issues like obesity and knee and hip osteoarthritis may also be barriers as they negatively impact self-efficacy related to PA participation (213). The built environment, or human-made surroundings, may also impact the ability and willingness to be regularly active (208), and may include availability of facilities, having pleasant and safe places to walk, and access to green spaces (214, 215). Focusing on creating more exercise-friendly environments is likely to promote greater participation. Setting realistic goals with appropriate activities, slower progression, and supportive feedback can increase success and confidence (216–218). Counseling by health care professionals may also be a meaningful and effective source of support (219). Likewise, supervision of exercise sessions improves compliance and glycemia (220).
The prevalence of physical inactivity, obesity, and T2D are significantly higher among non-Hispanic Blacks, American Indian/Alaskan Natives, and Hispanics than among non-Hispanic Whites (4, 221–224). The disproportionate burden of these conditions is likely more attributable to social and environmental determinants in these racial and ethnic minorities than biological differences (225, 226). Physical education in schools, limited open spaces for outdoor activities, inadequate infrastructure for active transportation, unsafe environments, and hypercaloric diets are dominant environmental factors that contribute to T2D development (225–232). Community environments that promote PA are associated with a lower incidence of T2D (227, 233–235); therefore, efforts that promote long-term health outcomes and target environmental factors may reduce T2D (235, 236). Neighborhood walkability, PA resources, and access to green spaces may reduce T2D risk (215, 235), while living in urban settings may raise it.
Expert Interpretation and Key Future Directions
Large scale clinical trials in T2D are needed to understand optimal treatment regimens and importance of PA and exercise, other lifestyle changes, and medications on glycemia.
Further work is warranted to elucidate the cognitive domains that are most responsive to PA and dietary improvements in adults with T2D, as well as exercise effects on memory and cognitive function related to glycemic management.
More research on the effect of exercise training on vascular function and the microbiome needs to be conducted in individuals with obesity and with and without T2D.
Longer duration training is needed to establish whether exercise timing modifies the glycemic response to meals as well as overnight levels and if specific time of day of planned exercise should be prescribed.
While prolonged sitting has been found deleterious in research settings, studies on PA breaks in daily life are necessary to determine whether long-term use has clinically relevant glycemic benefits in populations with T2D.
Potential interactions between diabetes medications like metformin and exercise training need to be further investigated with respect to their impact on glycemic management.
Social and environmental factors have also been associated with physical inactivity and the incidence of T2D and these factors need to be explored further.
Targeted research is needed to better define the health disparities that exist across racial, ethnic, and potentially socioeconomic populations and how their impact on PA participation for T2D and prediabetes prevention and management can be mitigated.
Larger clinical trials examining the impact of chronic high-intensity exercise on mitochondrial function and glucose tolerance in a population with obesity and with and without T2D are needed.
Conclusions
Various types of physical activity, inclusive of but not limited to planned exercise, can greatly enhance the health and glycemic management of individuals of all ages with T2D, including flexibility and balance exercise in adults. The latest Physical Activity Guidelines for Americans are applicable to most individuals with diabetes, including youth, with a few exceptions and modifications. All individuals should engage in regular physical activity, reduce sedentary time, and break up sitting time with frequent activity breaks. Physical activity undertaken with health complications can be made safe and efficacious, and exercise training undertaken before and after bariatric surgery is warranted and may enhances its health benefits. Finally, barriers to, and inequities in, physical activity and exercise adoption and maintenance need to be addressed to maximize participation.
Supplementary Material
Box:
• Regular aerobic exercise training improves glycemic management in adults with type 2 diabetes, with less daily time in hyperglycemia and 0.5–0.7% reductions in overall glycemia (as measured by A1C). |
• High-intensity resistance exercise training has greater beneficial effects than low-to-moderate-intensity resistance training in terms of overall glucose management and attenuation of insulin levels. |
• Greater energy expenditure postprandially reduces glucose levels regardless of exercise intensity or type, and durations ≥45 min provide the most consistent benefits. |
• Small “doses” of physical activity throughout the day to break up sitting modestly attenuate postprandial glucose and insulin levels, particularly in individuals with insulin resistance and a higher body mass index. |
• Weight loss (accomplished through lifestyle changes in diet and PA) of >5% appears to be necessary for beneficial effects on A1C, blood lipids, and blood pressure. |
• For reductions in visceral fat in individuals with type 2 diabetes, a moderately high volume of exercise (~500 kcal) done 4–5 days a week is needed. |
• In youth with type 2 diabetes, intensive lifestyle interventions plus metformin have not been superior to metformin alone in managing glycemia. |
• Despite the limited data, it is still recommended that youth and adolescents with type 2 diabetes meet the same physical activity goals set for youth in the general population. |
• Pregnant women with and without diabetes should participate in at least 20–30 minutes of moderate-intensity exercise most days of the week. |
• Individuals with type 2 diabetes using insulin or insulin secretagogues are advised to supplement with carbohydrate (or reduce insulin, if possible) as needed to prevent hypoglycemia during and after exercise. |
• Participation in an exercise program prior to bariatric surgery may enhance surgical outcomes, and after surgery participation confers additional benefits. |
Funding
C.C. is supported by the National Institute of Health grants: 1T34GM141989-01, 5UL1GM118964-07, 5TL4GM118965-07, 5RL5GM118963-07
J.A.K. is supported by the National Institute of Health R01 DK101513.
J.P.K. is supported by National Institute of Health grants: U54 GM104940, U54 GM104940-S2, U54 GM104940-S3, U01 DK114156, P01 HL103453, R01 HD088061, R01 DK114156.
S.K.M. is supported by National Institutes of Health R01-HL130296.
J.R.Z. was supported by the Swedish Research Council (Vetenskapsrådet) (2015-00165), the Strategic Research Program in Diabetes at Karolinska Institutet (2009-1068), the Swedish Research Council for Sport Science (P2018-0097), and Novo Nordisk Foundation (NNF17OC0030088).
Footnotes
This article is being published as an official pronouncement of the American College of Sports Medicine. This pronouncement was reviewed for the American College of Sports Medicine by members-at-large and the Pronouncements Committee.
Care has been taken to confirm the accuracy of the information present and to describe generally accepted practices. However, the authors, editors, and publisher are not responsible for errors or omissions or for any consequences from the application of the information in this publication and make no warranty, expressed or implied, with respect to the currency, completeness, or accuracy of the contents of the publication. The application of this information in a particular situation remains the professional responsibility of the practitioner; the clinical treatments described and recommended may not be considered absolute and universal recommendations.
Click here (***include URL) to download a slide deck that summarizes this ACSM Expert Consensus Statement on Exercise/Physical Activity and Type 2 Diabetes
COI Disclosures
MC is part of the Speakers Bureau for: Novo Nordisk, Boerhinger Ingelheim, Eli Lilly, and Medtronic. He has an affiliation with Diabetes Training Camp Foundation.
References
- 1.Colberg SR, Albright AL, Blissmer BJ, Braun B, Chasan-Taber L, Fernhall B, et al. Exercise and type 2 diabetes: American College of Sports Medicine and the American Diabetes Association: joint position statement. Exercise and type 2 diabetes. Med Sci Sports Exerc. 2010;42(12):2282–303. doi: 10.1249/MSS.0b013e3181eeb61c. [DOI] [PubMed] [Google Scholar]
- 2.Colberg SR, Sigal RJ, Fernhall B, Regensteiner JG, Blissmer BJ, Rubin RR, et al. Exercise and type 2 diabetes: the American College of Sports Medicine and the American Diabetes Association: joint position statement. Diabetes Care. 2010;33(12):e147–67. doi: 10.2337/dc10-9990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9(th) edition. Diabetes Res Clin Pract. 2019;157:107843. Epub 2019/09/14. doi: 10.1016/j.diabres.2019.107843. [DOI] [PubMed] [Google Scholar]
- 4.Centers for Disease Control and Prevention. National Diabetes Statistics Report, 2020. https://www.cdc.gov/diabetes/library/features/diabetes-stat-report.html.
- 5.2. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes-2021. Diabetes Care. 2021;44(Suppl 1):S15–s33. Epub 2020/12/11. doi: 10.2337/dc21-S002. [DOI] [PubMed] [Google Scholar]
- 6.Suh SH, Paik IY, Jacobs K. Regulation of blood glucose homeostasis during prolonged exercise. Mol Cells. 2007;23(3):272–9. Epub 2007/07/25. [PubMed] [Google Scholar]
- 7.Zierath JR, He L, Guma A, Odegoard Wahlstrom E, Klip A, Wallberg-Henriksson H. Insulin action on glucose transport and plasma membrane GLUT4 content in skeletal muscle from patients with NIDDM. Diabetologia. 1996;39(10):1180–9. Epub 1996/10/01. doi: 10.1007/BF02658504. [DOI] [PubMed] [Google Scholar]
- 8.Bajpeyi S, Tanner CJ, Slentz CA, Duscha BD, McCartney JS, Hickner RC, et al. Effect of exercise intensity and volume on persistence of insulin sensitivity during training cessation. Journal of applied physiology. 2009;106(4):1079–85. Epub 2009/02/07. doi: 10.1152/japplphysiol.91262.2008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Houmard JA, Tanner CJ, Slentz CA, Duscha BD, McCartney JS, Kraus WE. Effect of the volume and intensity of exercise training on insulin sensitivity. Journal of applied physiology. 2004;96(1):101–6. doi: 10.1152/japplphysiol.00707.2003. [DOI] [PubMed] [Google Scholar]
- 10.Kang J, Robertson RJ, Hagberg JM, Kelley DE, Goss FL, DaSilva SG, et al. Effect of exercise intensity on glucose and insulin metabolism in obese individuals and obese NIDDM patients. Diabetes Care. 1996;19(4):341–9. Epub 1996/04/01. doi: 10.2337/diacare.19.4.341. [DOI] [PubMed] [Google Scholar]
- 11.Heiskanen MA, Motiani KK, Mari A, Saunavaara V, Eskelinen JJ, Virtanen KA, et al. Exercise training decreases pancreatic fat content and improves beta cell function regardless of baseline glucose tolerance: a randomised controlled trial. Diabetologia. 2018;61(8):1817–28. Epub 2018/05/03. doi: 10.1007/s00125-018-4627-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Kirwan JP, Solomon TP, Wojta DM, Staten MA, Holloszy JO. Effects of 7 days of exercise training on insulin sensitivity and responsiveness in type 2 diabetes mellitus. Am J Physiol Endocrinol Metab. 2009;297(1):E151–6. doi: 10.1152/ajpendo.00210.2009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Magalhaes JP, Melo X, Correia IR, Ribeiro RT, Raposo J, Dores H, et al. Effects of combined training with different intensities on vascular health in patients with type 2 diabetes: a 1-year randomized controlled trial. Cardiovasc Diabetol. 2019;18(1):34. Epub 2019/03/20. doi: 10.1186/s12933-019-0840-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Naylor LH, Davis EA, Kalic RJ, Paramalingam N, Abraham MB, Jones TW, et al. Exercise training improves vascular function in adolescents with type 2 diabetes. Physiol Rep. 2016;4(4). Epub 2016/02/19. doi: 10.14814/phy2.12713. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Motiani KK, Collado MC, Eskelinen JJ, Virtanen KA, E LO, Salminen S, et al. Exercise Training Modulates Gut Microbiota Profile and Improves Endotoxemia. Med Sci Sports Exerc. 2020;52(1):94–104. Epub 2019/08/20. doi: 10.1249/MSS.0000000000002112. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Phielix E, Meex R, Moonen-Kornips E, Hesselink MK, Schrauwen P. Exercise training increases mitochondrial content and ex vivo mitochondrial function similarly in patients with type 2 diabetes and in control individuals. Diabetologia. 2010;53(8):1714–21. Epub 2010/04/28. doi: 10.1007/s00125-010-1764-2.. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Winnick JJ, Sherman WM, Habash DL, Stout MB, Failla ML, Belury MA, et al. Short-term aerobic exercise training in obese humans with type 2 diabetes mellitus improves whole-body insulin sensitivity through gains in peripheral, not hepatic insulin sensitivity. J Clin Endocrinol Metab. 2008;93(3):771–8. Epub 2007/12/13. doi: jc.2007-1524 [pii] 10.1210/jc.2007-1524 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Boulé NG, Haddad E, Kenny GP, Wells GA, Sigal RJ. Effects of exercise on glycemic control and body mass in type 2 diabetes mellitus: a meta-analysis of controlled clinical trials. JAMA. 2001;286(10):1218–27. [DOI] [PubMed] [Google Scholar]
- 19.Umpierre D, Ribeiro PA, Kramer CK, Leitao CB, Zucatti AT, Azevedo MJ, et al. Physical activity advice only or structured exercise training and association with HbA1c levels in type 2 diabetes: a systematic review and meta-analysis. JAMA. 2011;305(17):1790–9. doi: 10.1001/jama.2011.576. [DOI] [PubMed] [Google Scholar]
- 20.Chudyk A, Petrella RJ. Effects of exercise on cardiovascular risk factors in type 2 diabetes: a meta-analysis. Diabetes Care. 2011;34(5):1228–37. Epub 2011/04/29. doi: 34/5/1228 [pii] 10.2337/dc10-1881 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Snowling NJ, Hopkins WG. Effects of different modes of exercise training on glucose control and risk factors for complications in type 2 diabetic patients: a meta-analysis. Diabetes Care. 2006;29(11):2518–27. Epub 2006/10/27. doi: 29/11/2518 [pii] 10.2337/dc06-1317 [doi]. [DOI] [PubMed] [Google Scholar]
- 22.Borror A, Zieff G, Battaglini C, Stoner L. The Effects of Postprandial Exercise on Glucose Control in Individuals with Type 2 Diabetes: A Systematic Review. Sports Med. 2018;2(10):018–0864. [DOI] [PubMed] [Google Scholar]
- 23.Kadoglou NP, Iliadis F, Angelopoulou N, Perrea D, Ampatzidis G, Liapis CD, et al. The anti-inflammatory effects of exercise training in patients with type 2 diabetes mellitus. Eur J Cardiovasc Prev Rehabil. 2007;14(6):837–43. Epub 2007/11/29. doi: 10.1097/HJR.0b013e3282efaf50 [doi] 00149831-200712000-00019 [pii]. [DOI] [PubMed] [Google Scholar]
- 24.Boulé NG, Kenny GP, Haddad E, Wells GA, Sigal RJ. Meta-analysis of the effect of structured exercise training on cardiorespiratory fitness in Type 2 diabetes mellitus. Diabetologia. 2003;46(8):1071–81. [DOI] [PubMed] [Google Scholar]
- 25.Gordon BA, Benson AC, Bird SR, Fraser SF. Resistance training improves metabolic health in type 2 diabetes: a systematic review. Diabetes Res Clin Pract. 2009;83(2):157–75. Epub 2009/01/13. doi: S0168-8227(08)00587-1 [pii] 10.1016/j.diabres.2008.11.024 [doi]. [DOI] [PubMed] [Google Scholar]
- 26.Dunstan DW, Daly RM, Owen N, Jolley D, De Courten M, Shaw J, et al. High-intensity resistance training improves glycemic control in older patients with type 2 diabetes. Diabetes Care. 2002;25(10):1729–36. Epub 2002/09/28. [DOI] [PubMed] [Google Scholar]
- 27.Liu Y, Ye W, Chen Q, Zhang Y, Kuo CH, Korivi M. Resistance Exercise Intensity is Correlated with Attenuation of HbA1c and Insulin in Patients with Type 2 Diabetes: A Systematic Review and Meta-Analysis. Int J Environ Res Public Health. 2019;16(1).(pii):ijerph16010140. doi: 10.3390/ijerph. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Sigal RJ, Kenny GP, Boule NG, Wells GA, Prud’homme D, Fortier M, et al. Effects of aerobic training, resistance training, or both on glycemic control in type 2 diabetes: a randomized trial. Ann Intern Med. 2007;147(6):357–69. Epub 2007/09/19. doi: 147/6/357 [pii]. [DOI] [PubMed] [Google Scholar]
- 29.Church TS, Blair SN, Cocreham S, Johannsen N, Johnson W, Kramer K, et al. Effects of aerobic and resistance training on hemoglobin A1c levels in patients with type 2 diabetes: a randomized controlled trial. JAMA. 2010;304(20):2253–62. Epub 2010/11/26. doi: 304/20/2253 [pii] 10.1001/jama.2010.1710 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Schwingshackl L, Missbach B, Dias S, Konig J, Hoffmann G. Impact of different training modalities on glycaemic control and blood lipids in patients with type 2 diabetes: a systematic review and network meta-analysis. Diabetologia. 2014;57(9):1789–97. Epub 2014/07/06. doi: 10.1007/s00125-014-3303-z. [DOI] [PubMed] [Google Scholar]
- 31.Grace A, Chan E, Giallauria F, Graham PL, Smart NA. Clinical outcomes and glycaemic responses to different aerobic exercise training intensities in type II diabetes: a systematic review and meta-analysis. Cardiovasc Diabetol. 2017;16(1):37. Epub 2017/03/16. doi: 10.1186/s12933-017-0518-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Gillen JB, Little JP, Punthakee Z, Tarnopolsky MA, Riddell MC, Gibala MJ. Acute high-intensity interval exercise reduces the postprandial glucose response and prevalence of hyperglycaemia in patients with type 2 diabetes. Diabetes, obesity & metabolism. 2012;14(6):575–7. Epub 2012/01/25. doi: 10.1111/j.1463-1326.2012.01564.x. [DOI] [PubMed] [Google Scholar]
- 33.Savikj M, Gabriel BM, Alm PS, Smith J, Caidahl K, Bjornholm M, et al. Afternoon exercise is more efficacious than morning exercise at improving blood glucose levels in individuals with type 2 diabetes: a randomised crossover trial. Diabetologia. 2019;62(2):233–7. Epub 2018/11/15. doi: 10.1007/s00125-018-4767-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Karstoft K, Winding K, Knudsen SH, Nielsen JS, Thomsen C, Pedersen BK, et al. The effects of free-living interval-walking training on glycemic control, body composition, and physical fitness in type 2 diabetic patients: a randomized, controlled trial. Diabetes Care. 2013;36(2):228–36. doi: 10.2337/dc12-0658. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Nieuwoudt S, Fealy CE, Foucher JA, Scelsi AR, Malin SK, Pagadala M, et al. Functional high-intensity training improves pancreatic β-cell function in adults with type 2 diabetes. Am J Physiol Endocrinol Metab. 2017;313(3):E314–e20. Epub 2017/05/18. doi: 10.1152/ajpendo.00407.2016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Little JP, Gillen JB, Percival ME, Safdar A, Tarnopolsky MA, Punthakee Z, et al. Low-volume high-intensity interval training reduces hyperglycemia and increases muscle mitochondrial capacity in patients with type 2 diabetes. J Appl Physiol. 2011;111(6):1554–60. Epub 2011/08/27. doi: japplphysiol.00921.2011 [pii] 10.1152/japplphysiol.00921.2011 [doi]. [DOI] [PubMed] [Google Scholar]
- 37.Mitranun W, Deerochanawong C, Tanaka H, Suksom D. Continuous vs interval training on glycemic control and macro-and microvascular reactivity in type 2 diabetic patients. Scand J Med Sci Sports. 2014;24(2):e69–76. Epub 2013/10/10. doi: 10.1111/sms.12112. [DOI] [PubMed] [Google Scholar]
- 38.Hollekim-Strand SM, Bjorgaas MR, Albrektsen G, Tjonna AE, Wisloff U, Ingul CB. High-intensity interval exercise effectively improves cardiac function in patients with type 2 diabetes mellitus and diastolic dysfunction: a randomized controlled trial. J Am Coll Cardiol. 2014;64(16):1758–60. Epub 2014/10/18. doi: 10.1016/j.jacc.2014.07.971. [DOI] [PubMed] [Google Scholar]
- 39.Revdal A, Hollekim-Strand SM, Ingul CB. Can Time Efficient Exercise Improve Cardiometabolic Risk Factors in Type 2 Diabetes? A Pilot Study. J Sports Sci Med. 2016;15(2):308–13. Epub 2016/06/09. [PMC free article] [PubMed] [Google Scholar]
- 40.Ghardashi Afousi A, Izadi MR, Rakhshan K, Mafi F, Biglari S, Gandomkar Bagheri H. Improved brachial artery shear patterns and increased flow-mediated dilatation after low-volume high-intensity interval training in type 2 diabetes. Exp Physiol. 2018;103(9):1264–76. Epub 2018/06/23. doi: 10.1113/ep087005. [DOI] [PubMed] [Google Scholar]
- 41.Braun B, Zimmermann MB, Kretchmer N. Effects of exercise intensity on insulin sensitivity in women with non-insulin-dependent diabetes mellitus. J Appl Physiol. 1995;78(1):300–6. Epub 1995/01/01. [DOI] [PubMed] [Google Scholar]
- 42.Ryan BJ, Schleh MW, Ahn C, Ludzki AC, Gillen JB, Varshney P, et al. Moderate-Intensity Exercise and High-Intensity Interval Training Affect Insulin Sensitivity Similarly in Obese Adults. J Clin Endocrinol Metab. 2020;105(8):e2941–59. Epub 2020/06/04. doi: 10.1210/clinem/dgaa345. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Heiston EM, Eichner NZ, Gilbertson NM, Malin SK. Exercise improves adiposopathy, insulin sensitivity and metabolic syndrome severity independent of intensity. Exp Physiol. 2020;105(4):632–40. Epub 2020/02/06. doi: 10.1113/ep088158. [DOI] [PubMed] [Google Scholar]
- 44.Hansen D, Dendale P, Jonkers RA, Beelen M, Manders RJ, Corluy L, et al. Continuous low-to moderate-intensity exercise training is as effective as moderate- to high-intensity exercise training at lowering blood HbA(1c) in obese type 2 diabetes patients. Diabetologia. 2009;52(9):1789–97. Epub 2009/04/17. doi: 10.1007/s00125-009-1354-3 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Jelleyman C, Yates T, O’Donovan G, Gray LJ, King JA, Khunti K, et al. The effects of high-intensity interval training on glucose regulation and insulin resistance: a meta-analysis. Obes Rev. 2015;16(11):942–61. Epub 2015/10/21. doi: 10.1111/obr.12317. [DOI] [PubMed] [Google Scholar]
- 46.Innes KE, Selfe TK. Yoga for adults with type 2 diabetes: A systematic review of controlled trials. Journal of diabetes research. 2016;2016:6979370. Epub 2016/10/21. doi: 10.1155/2016/6979370. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Ahn S, Song R. Effects of Tai Chi Exercise on glucose control, neuropathy scores, balance, and quality of life in patients with type 2 diabetes and neuropathy. J Altern Complement Med. 2012;18(12):1172–8. Epub 2012/09/19. doi: 10.1089/acm.2011.0690. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Hamman RF, Wing RR, Edelstein SL, Lachin JM, Bray GA, Delahanty L, et al. Effect of weight loss with lifestyle intervention on risk of diabetes. Diabetes Care. 2006;29(9):2102–7. Epub 2006/08/29. doi: 29/9/2102 [pii] 10.2337/dc06-0560 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Knowler WC, Fowler SE, Hamman RF, Christophi CA, Hoffman HJ, Brenneman AT, et al. 10-year follow-up of diabetes incidence and weight loss in the Diabetes Prevention Program Outcomes Study. Lancet. 2009;374(9702):1677–86. Epub 2009/11/03. doi: 10.1016/s0140-6736(09)61457-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Long-term effects of lifestyle intervention or metformin on diabetes development and microvascular complications over 15-year follow-up: the Diabetes Prevention Program Outcomes Study. Lancet Diabetes Endocrinol. 2015;3(11):866–75. doi: 10.1016/S2213-8587(15)00291-0. Epub 2015 Sep 13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Kriska AM, Rockette-Wagner B, Edelstein SL, Bray GA, Delahanty LM, Hoskin MA, et al. The Impact of Physical Activity on the Prevention of Type 2 Diabetes: Evidence and Lessons Learned From the Diabetes Prevention Program, a Long-Standing Clinical Trial Incorporating Subjective and Objective Activity Measures. Diabetes Care. 2021;44(1):43–9. Epub 2021/01/15. doi: 10.2337/dc20-1129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Slentz CA, Bateman LA, Willis LH, Granville EO, Piner LW, Samsa GP, et al. Effects of exercise training alone vs a combined exercise and nutritional lifestyle intervention on glucose homeostasis in prediabetic individuals: a randomised controlled trial. Diabetologia. 2016;59(10):2088–98. Epub 2016/07/17. doi: 10.1007/s00125-016-4051-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Pi-Sunyer X, Blackburn G, Brancati FL, Bray GA, Bright R, Clark JM, et al. Reduction in weight and cardiovascular disease risk factors in individuals with type 2 diabetes: one-year results of the look AHEAD trial. Diabetes Care. 2007;30(6):1374–83. Epub 2007/03/17. doi: dc07-0048 [pii] 10.2337/dc07-0048. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Franz MJ, Boucher JL, Rutten-Ramos S, VanWormer JJ. Lifestyle weight-loss intervention outcomes in overweight and obese adults with type 2 diabetes: a systematic review and meta-analysis of randomized clinical trials. J Acad Nutr Diet. 2015;115(9):1447–63. Epub 2015/05/04. doi: 10.1016/j.jand.2015.02.031. [DOI] [PubMed] [Google Scholar]
- 55.Terranova CO, Brakenridge CL, Lawler SP, Eakin EG, Reeves MM. Effectiveness of lifestyle-based weight loss interventions for adults with type 2 diabetes: a systematic review and meta-analysis. Diabetes Obes Metab. 2015;17(4):371–8. Epub 2014/12/20. doi: 10.1111/dom.12430. [DOI] [PubMed] [Google Scholar]
- 56.Look ARG, Wing RR, Bolin P, Brancati FL, Bray GA, Clark JM, et al. Cardiovascular effects of intensive lifestyle intervention in type 2 diabetes. N Engl J Med. 2013;369(2):145–54. doi: 10.1056/NEJMoa1212914. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Espeland MA, Glick HA, Bertoni A, Brancati FL, Bray GA, Clark JM, et al. Impact of an intensive lifestyle intervention on use and cost of medical services among overweight and obese adults with type 2 diabetes: the action for health in diabetes. Diabetes Care. 2014;37(9):2548–56. Epub 2014/08/26. doi: 10.2337/dc14-0093. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Ross R, Dagnone D, Jones P, Smith H, Paddags A, Hudson R, et al. Reduction in obesity and related comorbid conditions after diet-induced weight loss or exercise-induced weight loss in men: a randomized controlled trial. Ann Intern Med. 2000;1333:92–103. [DOI] [PubMed] [Google Scholar]
- 59.Ross R, Janssen I, Dawson J, Kungle A-M, Kuk J, Wong S, et al. Exercise-induced reduction in obesity and insulin resistance in women: a randomized controlled trial. Obesity Research. 2004;12:789–98. [DOI] [PubMed] [Google Scholar]
- 60.Yassine HN, Marchetti CM, Krishnan RK, Vrobel TR, Gonzalez F, Kirwan JP. Effects of exercise and caloric restriction on insulin resistance and cardiometabolic risk factors in older obese adults--a randomized clinical trial. J Gerontol A Biol Sci Med Sci. 2009;64(1):90–5. Epub 2009/01/24. doi: 10.1093/gerona/gln032. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Giannopoulou I, Fernhall B, Carhart R, Weinstock R, Baynard T, Figueroa A, et al. Effects of diet and/or exercise on the adipocytokine and inflammatory cytokine levels of postmenopausal women with type 2 diabetes. Metabolism. 2005;54:866–75. [DOI] [PubMed] [Google Scholar]
- 62.Vounzoulaki E, Khunti K, Abner SC, Tan BK, Davies MJ, Gillies CL. Progression to type 2 diabetes in women with a known history of gestational diabetes: systematic review and meta-analysis. BMJ. 2020;369:m1361. Epub 2020/05/15. doi: 10.1136/bmj.m1361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.14. Management of Diabetes in Pregnancy: Standards of Medical Care in Diabetes-2021. Diabetes Care. 2021;44(Suppl 1):S200–s10. Epub 2020/12/11. doi: 10.2337/dc21-S014. [DOI] [PubMed] [Google Scholar]
- 64.Li Z, Cheng Y, Wang D, Chen H, Ming WK, Wang Z. Incidence Rate of Type 2 Diabetes Mellitus after Gestational Diabetes Mellitus: A Systematic Review and Meta-Analysis of 170,139 Women. J Diabetes Res. 2020;2020:3076463. Epub 2020/05/15. doi: 10.1155/2020/3076463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Dempsey JC, Butler CL, Sorensen TK, Lee IM, Thompson ML, Miller RS, et al. A case-control study of maternal recreational physical activity and risk of gestational diabetes mellitus. Diabetes Res Clin Pract. 2004;66(2):203–15. Epub 2004/11/10. doi: S0168822704001056 [pii] 10.1016/j.diabres.2004.03.010 [doi]. [DOI] [PubMed] [Google Scholar]
- 66.Dempsey JC, Sorensen TK, Williams MA, Lee IM, Miller RS, Dashow EE, et al. Prospective study of gestational diabetes mellitus risk in relation to maternal recreational physical activity before and during pregnancy. Am J Epidemiol. 2004;159(7):663–70. Epub 2004/03/23. [DOI] [PubMed] [Google Scholar]
- 67.Oken E, Ning Y, Rifas-Shiman SL, Radesky JS, Rich-Edwards JW, Gillman MW. Associations of physical activity and inactivity before and during pregnancy with glucose tolerance. Obstet Gynecol. 2006;108(5):1200–7. Epub 2006/11/02. doi: 108/5/1200 [pii] 10.1097/01.AOG.0000241088.60745.70 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Zhang C, Solomon CG, Manson JE, Hu FB. A prospective study of pregravid physical activity and sedentary behaviors in relation to the risk for gestational diabetes mellitus. Arch Intern Med. 2006;166(5):543–8. Epub 2006/03/15. doi: 166/5/543 [pii] 10.1001/archinte.166.5.543 [doi]. [DOI] [PubMed] [Google Scholar]
- 69.Barakat R, Refoyo I, Coteron J, Franco E. Exercise during pregnancy has a preventative effect on excessive maternal weight gain and gestational diabetes. A randomized controlled trial. Braz J Phys Ther. 2019;23(2):148–55. Epub 2018/11/25. doi: 10.1016/j.bjpt.2018.11.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Wang C, Wei Y, Zhang X, Zhang Y, Xu Q, Sun Y, et al. A randomized clinical trial of exercise during pregnancy to prevent gestational diabetes mellitus and improve pregnancy outcome in overweight and obese pregnant women. Am J Obstet Gynecol. 2017;216(4):340–51. Epub 2017/02/06. doi: 10.1016/j.ajog.2017.01.037. [DOI] [PubMed] [Google Scholar]
- 71.Davenport MH, Ruchat SM, Poitras VJ, Jaramillo Garcia A, Gray CE, Barrowman N, et al. Prenatal exercise for the prevention of gestational diabetes mellitus and hypertensive disorders of pregnancy: a systematic review and meta-analysis. Br J Sports Med. 2018;52(21):1367–75. Epub 2018/10/20. doi: 10.1136/bjsports-2018-099355. [DOI] [PubMed] [Google Scholar]
- 72.Sanabria-Martínez G, García-Hermoso A, Poyatos-León R, Álvarez-Bueno C, Sánchez-López M, Martínez-Vizcaíno V. Effectiveness of physical activity interventions on preventing gestational diabetes mellitus and excessive maternal weight gain: a meta-analysis. Bjog. 2015;122(9):1167–74. Epub 2015/06/04. doi: 10.1111/1471-0528.13429. [DOI] [PubMed] [Google Scholar]
- 73.Mottola MF, Davenport MH, Ruchat SM, Davies GA, Poitras VJ, Gray CE, et al. 2019 Canadian guideline for physical activity throughout pregnancy. Br J Sports Med. 2018;52(21):1339–46. Epub 2018/10/20. doi: 10.1136/bjsports-2018-100056. [DOI] [PubMed] [Google Scholar]
- 74.Gynecology ACoOa. ACOG Committee Opinion No. 650: Physical Activity and Exercise During Pregnancy and the Postpartum Period. Obstet Gynecol. 2015;126(6):e135–42. Epub 2015/11/26. doi: 10.1097/aog.0000000000001214. [DOI] [PubMed] [Google Scholar]
- 75.Craft LL, Perna FM. The Benefits of Exercise for the Clinically Depressed. Prim Care Companion J Clin Psychiatry. 2004;6(3):104–11. Epub 2004/09/14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Bettio LEB, Thacker JS, Rodgers SP, Brocardo PS, Christie BR, Gil-Mohapel J. Interplay between hormones and exercise on hippocampal plasticity across the lifespan. Biochim Biophys Acta Mol Basis Dis. 2020;1866(8):165821. Epub 2020/05/08. doi: 10.1016/j.bbadis.2020.165821. [DOI] [PubMed] [Google Scholar]
- 77.Williamson DA, Rejeski J, Lang W, Van Dorsten B, Fabricatore AN, Toledo K, et al. Impact of a weight management program on health-related quality of life in overweight adults with type 2 diabetes. Arch Intern Med. 2009;169(2):163–71. Epub 2009/01/28. doi: 169/2/163 [pii] 10.1001/archinternmed.2008.544 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Rubin RR, Wadden TA, Bahnson JL, Blackburn GL, Brancati FL, Bray GA, et al. Impact of intensive lifestyle intervention on depression and health-related quality of life in type 2 diabetes: the Look AHEAD Trial. Diabetes Care. 2014;37(6):1544–53. Epub 2014/05/24. doi: 10.2337/dc13-1928. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 79.MacDonald CS, Nielsen SM, Bjørner J, Johansen MY, Christensen R, Vaag A, et al. One-year intensive lifestyle intervention and improvements in health-related quality of life and mental health in persons with type 2 diabetes: a secondary analysis of the U-TURN randomized controlled trial. BMJ Open Diabetes Res Care. 2021;9(1). Epub 2021/01/15. doi: 10.1136/bmjdrc-2020-001840. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Palta P, Schneider AL, Biessels GJ, Touradji P, Hill-Briggs F. Magnitude of cognitive dysfunction in adults with type 2 diabetes: a meta-analysis of six cognitive domains and the most frequently reported neuropsychological tests within domains. J Int Neuropsychol Soc. 2014;20(3):278–91. Epub 2014/02/22. doi: 10.1017/s1355617713001483. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Robinson MM, Lowe VJ, Nair KS. Increased Brain Glucose Uptake After 12 Weeks of Aerobic High-Intensity Interval Training in Young and Older Adults. J Clin Endocrinol Metab. 2018;103(1):221–7. Epub 2017/10/28. doi: 10.1210/jc.2017-01571. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Honkala SM, Johansson J, Motiani KK, Eskelinen JJ, Virtanen KA, Löyttyniemi E, et al. Short-term interval training alters brain glucose metabolism in subjects with insulin resistance. J Cereb Blood Flow Metab. 2018;38(10):1828–38. Epub 2017/09/30. doi: 10.1177/0271678x17734998.. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 83.Kullmann S, Valenta V, Wagner R, Tschritter O, Machann J, Häring HU, et al. Brain insulin sensitivity is linked to adiposity and body fat distribution. Nat Commun. 2020;11(1):1841. Epub 2020/04/17. doi: 10.1038/s41467-020-15686-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.Espeland MA, Lipska K, Miller ME, Rushing J, Cohen RA, Verghese J, et al. Effects of Physical Activity Intervention on Physical and Cognitive Function in Sedentary Adults With and Without Diabetes. J Gerontol A Biol Sci Med Sci. 2017;72(6):861–6. Epub 2016/09/04. doi: 10.1093/gerona/glw179. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Yanagawa M, Umegaki H, Uno T, Oyun K, Kawano N, Maeno H, et al. Association between improvements in insulin resistance and changes in cognitive function in elderly diabetic patients with normal cognitive function. Geriatr Gerontol Int. 2011;11(3):341–7. Epub 2011/03/18. doi: 10.1111/j.1447-0594.2011.00691.x. [DOI] [PubMed] [Google Scholar]
- 86.Shellington EM, Reichert SM, Heath M, Gill DP, Shigematsu R, Petrella RJ. Results From a Feasibility Study of Square-Stepping Exercise in Older Adults With Type 2 Diabetes and Self-Reported Cognitive Complaints to Improve Global Cognitive Functioning. Can J Diabetes. 2018;42(6):603–12.e1. Epub 2018/06/10. doi: 10.1016/j.jcjd.2018.02.003. [DOI] [PubMed] [Google Scholar]
- 87.Baker LD, Frank LL, Foster-Schubert K, Green PS, Wilkinson CW, McTiernan A, et al. Aerobic exercise improves cognition for older adults with glucose intolerance, a risk factor for Alzheimer’s disease. J Alzheimers Dis. 2010;22(2):569–79. Epub 2010/09/18. doi: 10.3233/jad-2010-100768. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Espeland MA, Rapp SR, Bray GA, Houston DK, Johnson KC, Kitabchi AE, et al. Long-term impact of behavioral weight loss intervention on cognitive function. J Gerontol A Biol Sci Med Sci. 2014;69(9):1101–8. Epub 2014/03/13. doi: 10.1093/gerona/glu031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Cooke S, Pennington K, Jones A, Bridle C, Smith MF, Curtis F. Effects of exercise, cognitive, and dual-task interventions on cognition in type 2 diabetes mellitus: A systematic review and meta-analysis. PLoS One. 2020;15(5):e0232958. Epub 2020/05/15. doi: 10.1371/journal.pone.0232958. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Colberg SR, Somma CT, Sechrist SR. Physical activity participation may offset some of the negative impact of diabetes on cognitive function. J Am Med Dir Assoc. 2008;9(6):434–8. Epub 2008/07/01. doi: S1525-8610(08)00121-7 [pii] 10.1016/j.jamda.2008.03.014 [doi]. [DOI] [PubMed] [Google Scholar]
- 91.Devore EE, Kang JH, Okereke O, Grodstein F. Physical activity levels and cognition in women with type 2 diabetes. Am J Epidemiol. 2009;170(8):1040–7. Epub 2009/09/05. doi: 10.1093/aje/kwp224. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92.Piercy KL, Troiano RP, Ballard RM, Carlson SA, Fulton JE, Galuska DA, et al. The Physical Activity Guidelines for Americans. JAMA. 2018;320(19):2020–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 93.Powell KE, King AC, Buchner DM, Campbell WW, DiPietro L, Erickson KI, et al. The Scientific Foundation for the Physical Activity Guidelines for Americans, 2nd Edition. J Phys Act Health. 2018;17:1–11. [DOI] [PubMed] [Google Scholar]
- 94.Boulé NG, Weisnagel SJ, Lakka TA, Tremblay A, Bergman RN, Rankinen T, et al. Effects of exercise training on glucose homeostasis: the HERITAGE Family Study. Diabetes Care. 2005;28(1):108–14. [DOI] [PubMed] [Google Scholar]
- 95.King DS, Baldus PJ, Sharp RL, Kesl LD, Feltmeyer TL, Riddle MS. Time course for exercise-induced alterations in insulin action and glucose tolerance in middle-aged people. J Appl Physiol. 1995;78(1):17–22. Epub 1995/01/01. [DOI] [PubMed] [Google Scholar]
- 96.Colberg SR, Sigal RJ, Yardley JE, Riddell MC, Dunstan DW, Dempsey PC, et al. Physical Activity/Exercise and Diabetes: A Position Statement of the American Diabetes Association. Diabetes Care. 2016;39(11):2065–79. Epub 2016/12/08. doi: 10.2337/dc16-1728. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 97.Abate M, Schiavone C, Pelotti P, Salini V. Limited joint mobility in diabetes and ageing: recent advances in pathogenesis and therapy. Int J Immunopathol Pharmacol. 2011;23(4):997–1003. Epub 2011/01/20. doi: 4 [pii]. [DOI] [PubMed] [Google Scholar]
- 98.Herriott MT, Colberg SR, Parson HK, Nunnold T, Vinik AI. Effects of 8 weeks of flexibility and resistance training in older adults with type 2 diabetes. Diabetes care. 2004;27(12):2988–9. Epub 2004/11/25. doi: 27/12/2988 [pii]. [DOI] [PubMed] [Google Scholar]
- 99.Jayawardena R, Ranasinghe P, Chathuranga T, Atapattu PM, Misra A. The benefits of yoga practice compared to physical exercise in the management of type 2 Diabetes Mellitus: A systematic review and meta-analysis. Diabetes Metab Syndr. 2018;12(5):795–805. doi: 10.1016/j.dsx.2018.04.008. Epub Apr 18. [DOI] [PubMed] [Google Scholar]
- 100.Chapman A, Meyer C, Renehan E, Hill KD, Browning CJ. Exercise interventions for the improvement of falls-related outcomes among older adults with diabetes mellitus: A systematic review and meta-analyses. J Diabetes Complications. 2017;31(3):631–45. Epub 2016/10/22. doi: 10.1016/j.jdiacomp.2016.09.015. [DOI] [PubMed] [Google Scholar]
- 101.Pfeifer LO, Botton CE, Diefenthaeler F, Umpierre D, Pinto RS. Effects of a power training program in the functional capacity, on body balance and lower limb muscle strength of elderly with type 2 diabetes mellitus. J Sports Med Phys Fitness. 2021. Epub 2021/01/23. doi: 10.23736/s0022-4707.21.11880-8. [DOI] [PubMed] [Google Scholar]
- 102.Morrison S, Colberg SR, Mariano M, Parson HK, Vinik AI. Balance training reduces falls risk in older individuals with type 2 diabetes. Diabetes care. 2010;33(4):748–50. Epub 2010/01/26. doi: dc09-1699 [pii] 10.2337/dc09-1699 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103.Morrison S, Simmons R, Colberg SR, Parson HK, Vinik AI. Supervised Balance Training and Wii Fit-Based Exercises Lower Falls Risk in Older Adults With Type 2 Diabetes. Journal of the American Medical Directors Association. 2018;19(2):185.e7–.e13. Epub 2017/12/27. doi: 10.1016/j.jamda.2017.11.004. [DOI] [PubMed] [Google Scholar]
- 104.Cui J, Yan JH, Yan LM, Pan L, Le JJ, Guo YZ. Effects of yoga in adults with type 2 diabetes mellitus: A meta-analysis. J Diabetes Investig. 2017;8(2):201–9. Epub 2016/07/03. doi: 10.1111/jdi.12548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 105.Thind H, Lantini R, Balletto BL, Donahue ML, Salmoirago-Blotcher E, Bock BC, et al. The effects of yoga among adults with type 2 diabetes: A systematic review and meta-analysis. Prev Med. 2017;105:116–26. Epub 2017/09/04. doi: 10.1016/j.ypmed.2017.08.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 106.Chao M, Wang C, Dong X, Ding M. The Effects of Tai Chi on Type 2 Diabetes Mellitus: A Meta-Analysis. J Diabetes Res. 2018;2018:7350567.(doi): 10.1155/2018/7350567. eCollection 2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 107.Qin J, Chen Y, Guo S, You Y, Xu Y, Wu J, et al. Effect of Tai Chi on Quality of Life, Body Mass Index, and Waist-Hip Ratio in Patients With Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis. Front Endocrinol (Lausanne). 2020;11:543627. Epub 2021/02/06. doi: 10.3389/fendo.2020.543627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 108.Cai H, Li G, Jiang S, Yin H, Liu P, Chen L. Effect of Low-Intensity, Kinect™-Based Kaimai-Style Qigong Exercise in Older Adults With Type 2 Diabetes. J Gerontol Nurs. 2019;45(2):42–52. Epub 2019/01/29. doi: 10.3928/00989134-20190111-05. [DOI] [PubMed] [Google Scholar]
- 109.Meng D, Chunyan W, Xiaosheng D, Xiangren Y. The Effects of Qigong on Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis. Evid Based Complement Alternat Med. 2018;2018:8182938.(doi): 10.1155/2018/8182938. eCollection 2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Melo KCB, Araújo FS, Cordeiro Júnior CCM, de Andrade KTP, Moreira SR. Pilates Method Training: Functional and Blood Glucose Responses of Older Women With Type 2 Diabetes. J Strength Cond Res. 2020;34(4):1001–7. Epub 2018/07/10. doi: 10.1519/jsc.0000000000002704. [DOI] [PubMed] [Google Scholar]
- 111.Larsen BA, Martin L, Strong DR. Sedentary behavior and prevalent diabetes in Non-Latino Whites, Non-Latino Blacks and Latinos: findings from the National Health Interview Survey. J Public Health (Oxf). 2015;37(4):634–40. Epub 2014/12/30. doi: 10.1093/pubmed/fdu103. [DOI] [PubMed] [Google Scholar]
- 112.van der Berg JD, Stehouwer CD, Bosma H, van der Velde JH, Willems PJ, Savelberg HH, et al. Associations of total amount and patterns of sedentary behaviour with type 2 diabetes and the metabolic syndrome: The Maastricht Study. Diabetologia. 2016;59(4):709–18. Epub 2016/02/03. doi: 10.1007/s00125-015-3861-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 113.Cooper AJ, Brage S, Ekelund U, Wareham NJ, Griffin SJ, Simmons RK. Association between objectively assessed sedentary time and physical activity with metabolic risk factors among people with recently diagnosed type 2 diabetes. Diabetologia. 2014;57(1):73–82. Epub 2013/11/08. doi: 10.1007/s00125-013-3069-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 114.Nauman J, Stensvold D, Coombes JS, Wisløff U. Cardiorespiratory Fitness, Sedentary Time, and Cardiovascular Risk Factor Clustering. Med Sci Sports Exerc. 2016;48(4):625–32. Epub 2015/11/21. doi: 10.1249/mss.0000000000000819.. [DOI] [PubMed] [Google Scholar]
- 115.Dempsey PC, Larsen RN, Sethi P, Sacre JW, Straznicky NE, Cohen ND, et al. Benefits for Type 2 Diabetes of Interrupting Prolonged Sitting With Brief Bouts of Light Walking or Simple Resistance Activities. Diabetes Care. 2016;39(6):964–72. Epub 2016/05/22. doi: 10.2337/dc15-2336. [DOI] [PubMed] [Google Scholar]
- 116.Duvivier BM, Schaper NC, Hesselink MK, van Kan L, Stienen N, Winkens B, et al. Breaking sitting with light activities vs structured exercise: a randomised crossover study demonstrating benefits for glycaemic control and insulin sensitivity in type 2 diabetes. Diabetologia. 2017;60(3):490–8. Epub 2016/12/03. doi: 10.1007/s00125-016-4161-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 117.Honda H, Igaki M, Hatanaka Y, Komatsu M, Tanaka S, Miki T, et al. Stair climbing/descending exercise for a short time decreases blood glucose levels after a meal in people with type 2 diabetes. BMJ Open Diabetes Res Care. 2016;4(1):e000232. Epub 2016/08/23. doi: 10.1136/bmjdrc-2016-000232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 118.Honda H, Igaki M, Hatanaka Y, Komatsu M, Tanaka SI, Miki T, et al. Repeated 3-minute stair climbing-descending exercise after a meal over 2 weeks increases serum 1,5-anhydroglucitol levels in people with type 2 diabetes. J Phys Ther Sci. 2017;29(1):75–8. Epub 2017/02/18. doi: 10.1589/jpts.29.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 119.Godkin FE, Jenkins EM, Little JP, Nazarali Z, Percival ME, Gibala MJ. The effect of brief intermittent stair climbing on glycemic control in people with type 2 diabetes: a pilot study. Appl Physiol Nutr Metab. 2018;43(9):969–72. Epub 2018/05/03. doi: 10.1139/apnm-2018-0135. [DOI] [PubMed] [Google Scholar]
- 120.Holmstrup M, Fairchild T, Keslacy S, Weinstock R, Kanaley J. Multiple short bouts of exercise over 12-h period reduce glucose excursions more than an energy-matched single bout of exercise. Metabolism. 2014;63(4):510–9. doi: 10.1016/j.metabol.2013.12.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 121.Francois ME, Baldi JC, Manning PJ, Lucas SJ, Hawley JA, Williams MJ, et al. ‘Exercise snacks’ before meals: a novel strategy to improve glycaemic control in individuals with insulin resistance. Diabetologia. 2014;57(7):1437–45. Epub 2014/05/13. doi: 10.1007/s00125-014-3244-6. [DOI] [PubMed] [Google Scholar]
- 122.Loh R, Stamatakis E, Folkerts D, Allgrove JE, Moir HJ. Effects of Interrupting Prolonged Sitting with Physical Activity Breaks on Blood Glucose, Insulin and Triacylglycerol Measures: A Systematic Review and Meta-analysis. Sports Med. 2020;50(2):295–330. Epub 2019/09/26. doi: 10.1007/s40279-019-01183-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123.Blankenship JM, Chipkin SR, Freedson PS, Staudenmayer J, Lyden K, Braun B. Managing free-living hyperglycemia with exercise or interrupted sitting in type 2 diabetes. J Appl Physiol (1985). 2019;126(3):616–25. Epub 2018/12/21. doi: 10.1152/japplphysiol.00389.2018. [DOI] [PubMed] [Google Scholar]
- 124.Nadeau KJ, Anderson BJ, Berg EG, Chiang JL, Chou H, Copeland KC, et al. Youth-Onset Type 2 Diabetes Consensus Report: Current Status, Challenges, and Priorities. Diabetes Care. 2016;39(9):1635–42. Epub 2016/08/04. doi: 10.2337/dc16-1066. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 125.Savoye M, Caprio S, Dziura J, Camp A, Germain G, Summers C, et al. Reversal of early abnormalities in glucose metabolism in obese youth: results of an intensive lifestyle randomized controlled trial. Diabetes Care. 2014;37(2):317–24. Epub 2013/09/26. doi: 10.2337/dc13-1571. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 126.Group TS. Effects of metformin, metformin plus rosiglitazone, and metformin plus lifestyle on insulin sensitivity and beta-cell function in TODAY. Diabetes Care. 2013;36(6):1749–57. Epub 2013/05/25. doi: 10.2337/dc12-2393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 127.Group TS, Zeitler P, Hirst K, Pyle L, Linder B, Copeland K, et al. A clinical trial to maintain glycemic control in youth with type 2 diabetes. N Engl J Med. 2012;366(24):2247–56. Epub 2012/05/01. doi: 10.1056/NEJMoa1109333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 128.Armstrong MJ, Rabi DM, Southern DA, Nanji A, Ghali WA, Sigal RJ. Clinical Utility of Pre-Exercise Stress Testing in People With Diabetes. Can J Cardiol. 2019;35(2):185–92. Epub 2019/02/15. doi: 10.1016/j.cjca.2018.11.007. [DOI] [PubMed] [Google Scholar]
- 129.Curtis JM, Horton ES, Bahnson J, Gregg EW, Jakicic JM, Regensteiner JG, et al. Prevalence and predictors of abnormal cardiovascular responses to exercise testing among individuals with type 2 diabetes: the Look AHEAD (Action for Health in Diabetes) study. Diabetes Care. 2010;33(4):901–7. Epub 2010/01/09. doi: 10.2337/dc09-1787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 130.Young LH, Wackers FJ, Chyun DA, Davey JA, Barrett EJ, Taillefer R, et al. Cardiac outcomes after screening for asymptomatic coronary artery disease in patients with type 2 diabetes: the DIAD study: a randomized controlled trial. JAMA. 2009;301(15):1547–55. Epub 2009/04/16. doi: 301/15/1547 [pii] 10.1001/jama.2009.476 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 131.Featherstone JF, Holly RG, Amsterdam EA. Physiologic responses to weight lifting in coronary artery disease. Am J Cardiol. 1993;71(4):287–92. Epub 1993/02/01. [DOI] [PubMed] [Google Scholar]
- 132.Ghilarducci LE, Holly RG, Amsterdam EA. Effects of high resistance training in coronary artery disease. Am J Cardiol. 1989;64(14):866–70. Epub 1989/10/15. [DOI] [PubMed] [Google Scholar]
- 133.Wenger NK, Froelicher ES, Smith LK, Ades PA, Berra K, Blumenthal JA, et al. Cardiac rehabilitation as secondary prevention. Agency for Health Care Policy and Research and National Heart, Lung, and Blood Institute. Clin Pract Guidel Quick Ref Guide Clin. 1995(17):1–23. Epub 1995/10/01. [PubMed] [Google Scholar]
- 134.Sigal RJ, Kenny GP, Wasserman DH, Castaneda-Sceppa C. Physical activity/exercise and type 2 diabetes. Diabetes Care. 2004;27(10):2518–39. Epub 2004/09/29. doi: 10.2337/diacare.27.10.2518. [DOI] [PubMed] [Google Scholar]
- 135.Kennedy JW, Hirshman MF, Gervino EV, Ocel JV, Forse RA, Hoenig SJ, et al. Acute exercise induces GLUT4 translocation in skeletal muscle of normal human subjects and subjects with type 2 diabetes. Diabetes. 1999;48(5):1192–7. Epub 1999/05/20. doi: 10.2337/diabetes.48.5.1192. [DOI] [PubMed] [Google Scholar]
- 136.Musi N, Fujii N, Hirshman MF, Ekberg I, Froberg S, Ljungqvist O, et al. AMP-activated protein kinase (AMPK) is activated in muscle of subjects with type 2 diabetes during exercise. Diabetes. 2001;50(5):921–7. Epub 2001/05/04. doi: 10.2337/diabetes.50.5.921. [DOI] [PubMed] [Google Scholar]
- 137.Rosenstock J, Hassman DR, Madder RD, Brazinsky SA, Farrell J, Khutoryansky N, et al. Repaglinide versus nateglinide monotherapy: a randomized, multicenter study. Diabetes Care. 2004;27(6):1265–70. Epub 2004/05/27. doi: 10.2337/diacare.27.6.1265. [DOI] [PubMed] [Google Scholar]
- 138.Larsen JJ, Dela F, Madsbad S, Vibe-Petersen J, Galbo H. Interaction of sulfonylureas and exercise on glucose homeostasis in type 2 diabetic patients. Diabetes Care. 1999;22(10):1647–54. Epub 1999/10/20. doi: 10.2337/diacare.22.10.1647. [DOI] [PubMed] [Google Scholar]
- 139.Riddell MC, Gallen IW, Smart CE, Taplin CE, Adolfsson P, Lumb AN, et al. Exercise management in type 1 diabetes: a consensus statement. Lancet Diabetes Endocrinol. 2017;5(5):377–90. Epub 2017/01/28. doi: 10.1016/S2213-8587(17)30014-1. [DOI] [PubMed] [Google Scholar]
- 140.Gordon BA, Bird SR, MacIsaac RJ, Benson AC. Does a single bout of resistance or aerobic exercise after insulin dose reduction modulate glycaemic control in type 2 diabetes? A randomised cross-over trial. J Sci Med Sport. 2016. Epub 2016/02/26. doi: 10.1016/j.jsams.2016.01.004. [DOI] [PubMed] [Google Scholar]
- 141.Kjaer M, Hollenbeck CB, Frey-Hewitt B, Galbo H, Haskell W, Reaven GM. Glucoregulation and hormonal responses to maximal exercise in non-insulin-dependent diabetes. J Appl Physiol. 1990;68(5):2067–74. Epub 1990/05/01. [DOI] [PubMed] [Google Scholar]
- 142.Hernandez-Quiles C, Ramirez-Duque N, Acosta-Delgado D. Ketoacidosis Due to Empagliflozin, a Paradigm Shift: Case Report and Review of Literature. Curr Diabetes Rev. 2019;15(4):259–62. Epub 2018/07/27. doi: 10.2174/1573399814666180726114044. [DOI] [PubMed] [Google Scholar]
- 143.Notley SR, Poirier MP, Hardcastle SG, Flouris AD, Boulay P, Sigal RJ, et al. Aging Impairs Whole-Body Heat Loss in Women under Both Dry and Humid Heat Stress. Med Sci Sports Exerc. 2017;49(11):2324–32. Epub 2017/10/19. doi: 10.1249/mss.0000000000001342. [DOI] [PubMed] [Google Scholar]
- 144.Poirier MP, Notley SR, Boulay P, Sigal RJ, Friesen BJ, Malcolm J, et al. Type 2 diabetes does not exacerbate body heat storage in older adults during brief, extreme passive heat exposure. Temperature (Austin). 2020;7(3):263–9. Epub 2020/10/31. doi: 10.1080/23328940.2020.1736760. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 145.Notley SR, Poirier MP, Sigal RJ, D’Souza A, Flouris AD, Fujii N, et al. Exercise heat stress in patients with and without Type 2 Diabetes. Jama. 2019;322(14):1409–11. Epub 2019/10/09. doi: 10.1001/jama.2019.10943. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 146.Kenny GP, Stapleton JM, Yardley JE, Boulay P, Sigal RJ. Older adults with type 2 diabetes store more heat during exercise. Med Sci Sports Exerc. 2013;45(10):1906–14. Epub 2013/04/02. doi: 10.1249/MSS.0b013e3182940836. [DOI] [PubMed] [Google Scholar]
- 147.Layton JB, Li W, Yuan J, Gilman JP, Horton DB, Setoguchi S. Heatwaves, medications, and heat-related hospitalization in older Medicare beneficiaries with chronic conditions. PLoS One. 2020;15(12):e0243665. Epub 2020/12/11. doi: 10.1371/journal.pone.0243665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 148.de Lemos Muller CH, Rech A, Botton CE, Schroeder HT, Bock PM, Farinha JB, et al. Heat-induced extracellular HSP72 release is blunted in elderly diabetic people compared with healthy middle-aged and older adults, but it is partially restored by resistance training. Exp Gerontol. 2018;111:180–7. Epub 2018/07/28. doi: 10.1016/j.exger.2018.07.014. [DOI] [PubMed] [Google Scholar]
- 149.Macartney MJ, Notley SR, Herry CL, Sigal RJ, Boulay P, Kenny GP. Effect of exercise-heat acclimation on cardiac autonomic modulation in type 2 diabetes: a pilot study. Appl Physiol Nutr Metab. 2021;46(3):284–7. Epub 2020/11/18. doi: 10.1139/apnm-2020-0785. [DOI] [PubMed] [Google Scholar]
- 150.11. Microvascular Complications and Foot Care: Standards of Medical Care in Diabetes-2021. Diabetes Care. 2021;44(Suppl 1):S151–s67. Epub 2020/12/11. doi: 10.2337/dc21-S011. [DOI] [PubMed] [Google Scholar]
- 151.10. Cardiovascular Disease and Risk Management: Standards of Medical Care in Diabetes-2021. Diabetes Care. 2021;44(Suppl 1):S125–s50. Epub 2020/12/11. doi: 10.2337/dc21-S010. [DOI] [PubMed] [Google Scholar]
- 152.Rossboth S, Lechleitner M, Oberaigner W. Risk factors for diabetic foot complications in type 2 diabetes-A systematic review. Endocrinol Diabetes Metab. 2021;4(1):e00175. Epub 2021/02/04. doi: 10.1002/edm2.175. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 153.Biswas A, Oh PI, Faulkner GE, Bajaj RR, Silver MA, Mitchell MS, et al. Sedentary time and its association with risk for disease incidence, mortality, and hospitalization in adults: a systematic review and meta-analysis. Ann Intern Med. 2015;162(2):123–32. Epub 2015/01/20. doi: 10.7326/m14-1651. [DOI] [PubMed] [Google Scholar]
- 154.Wilmot EG, Edwardson CL, Achana FA, Davies MJ, Gorely T, Gray LJ, et al. Sedentary time in adults and the association with diabetes, cardiovascular disease and death: systematic review and meta-analysis. Diabetologia. 2012;55(11):2895–905. Epub 2012/08/15. doi: 10.1007/s00125-012-2677-z. [DOI] [PubMed] [Google Scholar]
- 155.Riebe D, Franklin BA, Thompson PD, Garber CE, Whitfield GP, Magal M, et al. Updating ACSM’s Recommendations for Exercise Preparticipation Health Screening. Med Sci Sports Exerc. 2015;47(11):2473–9. Epub 2015/10/17. doi: 10.1249/mss.0000000000000664. [DOI] [PubMed] [Google Scholar]
- 156.Derave W, Mertens A, Muls E, Pardaens K, Hespel P. Effects of post-absorptive and postprandial exercise on glucoregulation in metabolic syndrome. Obesity (Silver Spring). 2007;15(3):704–11. Epub 2007/03/21. doi: 10.1038/oby.2007.548. [DOI] [PubMed] [Google Scholar]
- 157.Larsen JJ, Dela F, Madsbad S, Galbo H. The effect of intense exercise on postprandial glucose homeostasis in type II diabetic patients. Diabetologia. 1999;42(11):1282–92. doi: 10.1007/s001250051440. [DOI] [PubMed] [Google Scholar]
- 158.Poirier P, Mawhinney S, Grondin L, Tremblay A, Broderick T, Cleroux J, et al. Prior meal enhances the plasma glucose lowering effect of exercise in type 2 diabetes. Med Sci Sports Exerc. 2001;33(8):1259–64. [DOI] [PubMed] [Google Scholar]
- 159.Terada T, Wilson BJ, Myette-Cote E, Kuzik N, Bell GJ, McCargar LJ, et al. Targeting specific interstitial glycemic parameters with high-intensity interval exercise and fasted-state exercise in type 2 diabetes. Metabolism. 2016;65(5):599–608. Epub 2016/04/18. doi: 10.1016/j.metabol.2016.01.003. [DOI] [PubMed] [Google Scholar]
- 160.Teo SYM, Kanaley JA, Guelfi KJ, Marston KJ, Fairchild TJ. The Effect of Exercise Timing on Glycemic Control: A Randomized Clinical Trial. Med Sci Sports Exerc. 2020;52(2):323–34. Epub 2019/09/04. doi: 10.1249/MSS.0000000000002139. [DOI] [PubMed] [Google Scholar]
- 161.Colberg SR, Zarrabi L, Bennington L, Nakave A, Thomas Somma C, Swain DP, et al. Postprandial walking is better for lowering the glycemic effect of dinner than pre-dinner exercise in type 2 diabetic individuals. Journal of the American Medical Directors Association. 2009;10(6):394–7. doi: 10.1016/j.jamda.2009.03.015. [DOI] [PubMed] [Google Scholar]
- 162.Heden TD, Winn NC, Mari A, Booth FW, Rector RS, Thyfault JP, et al. Postdinner resistance exercise improves postprandial risk factors more effectively than predinner resistance exercise in patients with type 2 diabetes. Journal of applied physiology. 2015;118(5):624–34. Epub 2014/12/30. doi: 10.1152/japplphysiol.00917.2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 163.USDA, Services HaH. Dietary Guidelines for Americans, 2020–2025. 9th ed December 2020. [Google Scholar]
- 164.van der Schaft N, Schoufour JD, Nano J, Kiefte-de Jong JC, Muka T, Sijbrands EJG, et al. Dietary antioxidant capacity and risk of type 2 diabetes mellitus, prediabetes and insulin resistance: the Rotterdam Study. Eur J Epidemiol. 2019;34(9):853–61. Epub 2019/08/11. doi: 10.1007/s10654-019-00548-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 165.Feinman RD, Pogozelski WK, Astrup A, Bernstein RK, Fine EJ, Westman EC, et al. Dietary carbohydrate restriction as the first approach in diabetes management: critical review and evidence base. Nutrition (Burbank, Los Angeles County, Calif). 2015;31(1):1–13. Epub 2014/07/16. doi: 10.1016/j.nut.2014.06.011. [DOI] [PubMed] [Google Scholar]
- 166.Lennerz BS, Koutnik AP, Azova S, Wolfsdorf JI, Ludwig DS. Carbohydrate restriction for diabetes: rediscovering centuries-old wisdom. J Clin Invest. 2021;131(1). Epub 2021/01/05. doi: 10.1172/jci142246. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 167.Kirk JK, Graves DE, Craven TE, Lipkin EW, Austin M, Margolis KL. Restricted-carbohydrate diets in patients with type 2 diabetes: a meta-analysis. J Am Diet Assoc. 2008;108(1):91–100. Epub 2007/12/25. doi: 10.1016/j.jada.2007.10.003. [DOI] [PubMed] [Google Scholar]
- 168.Powers MA, Bardsley J, Cypress M, Duker P, Funnell MM, Fischl AH, et al. Diabetes Self-Management Education and Support in Type 2 Diabetes: A Joint Position Statement of the American Diabetes Association, the American Association of Diabetes Educators, and the Academy of Nutrition and Dietetics. J Acad Nutr Diet. 2015;115(8):1323–34. Epub 2015/06/10. doi: 10.1016/j.jand.2015.05.012. [DOI] [PubMed] [Google Scholar]
- 169.Chester B, Babu JR, Greene MW, Geetha T. The effects of popular diets on type 2 diabetes management. Diabetes Metab Res Rev. 2019;35(8):e3188. Epub 2019/05/24. doi: 10.1002/dmrr.3188. [DOI] [PubMed] [Google Scholar]
- 170.Paoli A, Rubini A, Volek JS, Grimaldi KA. Beyond weight loss: a review of the therapeutic uses of very-low-carbohydrate (ketogenic) diets. Eur J Clin Nutr. 2013;67(8):789–96. Epub 2013/06/27. doi: 10.1038/ejcn.2013.116. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 171.Burke LM. Re-Examining High-Fat Diets for Sports Performance: Did We Call the ‘Nail in the Coffin’ Too Soon? Sports Med. 2015;45 Suppl 1(Suppl 1):S33–49. Epub 2015/11/11. doi: 10.1007/s40279-015-0393-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 172.McSwiney FT, Wardrop B, Hyde PN, Lafountain RA, Volek JS, Doyle L. Keto-adaptation enhances exercise performance and body composition responses to training in endurance athletes. Metabolism: clinical and experimental. 2018;81:25–34. Epub 2017/11/03. doi: 10.1016/j.metabol.2017.10.010. [DOI] [PubMed] [Google Scholar]
- 173.Wroble KA, Trott MN, Schweitzer GG, Rahman RS, Kelly PV, Weiss EP. Low-carbohydrate, ketogenic diet impairs anaerobic exercise performance in exercise-trained women and men: a randomized-sequence crossover trial. J Sports Med Phys Fitness. 2019;59(4):600–7. Epub 2018/04/06. doi: 10.23736/s0022-4707.18.08318-4. [DOI] [PubMed] [Google Scholar]
- 174.Sharoff CG, Hagobian TA, Malin SK, Chipkin SR, Yu H, Hirshman MF, et al. Combining short-term metformin treatment and one bout of exercise does not increase insulin action in insulin-resistant individuals. Am J Physiol Endocrinol Metab. 2010;298(4):E815–23. Epub 2010/01/15. doi: 10.1152/ajpendo.00517.2009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 175.Malin SK, Gerber R, Chipkin SR, Braun B. Independent and combined effects of exercise training and metformin on insulin sensitivity in individuals with prediabetes. Diabetes Care. 2012;35(1):131–6. Epub 2011/11/02. doi: dc11-0925 [pii] 10.2337/dc11-0925 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 176.Boule NG, Robert C, Bell GJ, Johnson ST, Bell RC, Lewanczuk RZ, et al. Metformin and exercise in type 2 diabetes: examining treatment modality interactions. Diabetes Care. 2011;34(7):1469–74. Epub 2011/05/24. doi: dc10-2207 [pii] 10.2337/dc10-2207 [doi]. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 177.Hällsten K, Virtanen KA, Lönnqvist F, Sipilä H, Oksanen A, Viljanen T, et al. Rosiglitazone but not metformin enhances insulin-and exercise-stimulated skeletal muscle glucose uptake in patients with newly diagnosed type 2 diabetes. Diabetes. 2002;51(12):3479–85. Epub 2002/11/28. doi: 10.2337/diabetes.51.12.3479. [DOI] [PubMed] [Google Scholar]
- 178.Ortega JF, Morales-Palomo F, Ramirez-Jimenez M, Moreno-Cabañas A, Mora-Rodríguez R. Exercise improves metformin 72-h glucose control by reducing the frequency of hyperglycemic peaks. Acta Diabetol. 2020;57(6):715–23. Epub 2020/02/06. doi: 10.1007/s00592-020-01488-7. [DOI] [PubMed] [Google Scholar]
- 179.Konopka AR, Laurin JL, Schoenberg HM, Reid JJ, Castor WM, Wolff CA, et al. Metformin inhibits mitochondrial adaptations to aerobic exercise training in older adults. Aging Cell. 2019;18(1):e12880. Epub 2018/12/15. doi: 10.1111/acel.12880. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 180.Walton RG, Dungan CM, Long DE, Tuggle SC, Kosmac K, Peck BD, et al. Metformin blunts muscle hypertrophy in response to progressive resistance exercise training in older adults: A randomized, double-blind, placebo-controlled, multicenter trial: The MASTERS trial. Aging Cell. 2019;18(6):e13039. Epub 2019/09/27. doi: 10.1111/acel.13039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 181.Malin SK, Stewart NR. Metformin may contribute to inter-individual variability for glycemic responses to exercise. Front Endocrinol (Lausanne). 2020;11:519. Epub 2020/08/28. doi: 10.3389/fendo.2020.00519. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 182.Mensberg P, Nyby S, Jørgensen PG, Storgaard H, Jensen MT, Sivertsen J, et al. Near-normalization of glycaemic control with glucagon-like peptide-1 receptor agonist treatment combined with exercise in patients with type 2 diabetes. Diabetes Obes Metab. 2017;19(2):172–80. Epub 2016/11/05. doi: 10.1111/dom.12797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 183.van Dijk JW, Tummers K, Stehouwer CD, Hartgens F, van Loon LJ. Exercise therapy in type 2 diabetes: is daily exercise required to optimize glycemic control? Diabetes Care. 2012;35(5):948–54. doi: 10.2337/dc11-2112. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 184.Sigal RJ, Fisher SJ, Halter JB, Vranic M, Marliss EB. Glucoregulation during and after intense exercise: effects of beta-adrenergic blockade in subjects with type 1 diabetes mellitus. J Clin Endocrinol Metab. 1999;84(11):3961–71. Epub 1999/11/24. [DOI] [PubMed] [Google Scholar]
- 185.de Muinck ED, Lie KI. Safety and efficacy of beta-blockers in the treatment of stable angina pectoris. J Cardiovasc Pharmacol. 1990;16 Suppl 5:S123–8. Epub 1990/01/01. [PubMed] [Google Scholar]
- 186.Colberg SR, Swain DP, Vinik AI. Use of heart rate reserve and rating of perceived exertion to prescribe exercise intensity in diabetic autonomic neuropathy. Diabetes Care. 2003;26(4):986–90. [DOI] [PubMed] [Google Scholar]
- 187.Nichols GA, Koro CE. Does statin therapy initiation increase the risk for myopathy? An observational study of 32,225 diabetic and nondiabetic patients. Clin Ther. 2007;29(8):1761–70. Epub 2007/10/09. doi: S0149-2918(07)00257-3 [pii] 10.1016/j.clinthera.2007.08.022 [doi]. [DOI] [PubMed] [Google Scholar]
- 188.Mingrone G, Panunzi S, De Gaetano A, Guidone C, Iaconelli A, Capristo E, et al. Metabolic surgery versus conventional medical therapy in patients with type 2 diabetes: 10-year follow-up of an open-label, single-centre, randomised controlled trial. Lancet. 2021;397:293–304. [DOI] [PubMed] [Google Scholar]
- 189.Schauer PR, Bhatt DL, Kirwan JP, Wolski K, Aminian A, Brethauer SA, et al. Bariatric Surgery versus Intensive Medical Therapy for Diabetes - 5-Year Outcomes. N Engl J Med. 2017;376(7):641–51. Epub 2017/02/16. doi: 10.1056/NEJMoa1600869. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 190.Bond DS, Jakicic JM, Unick JL, Vithiananthan S, Pohl D, Roye GD, et al. Pre- to postoperative physical activity changes in bariatric surgery patients: self report vs. objective measures. Obesity (Silver Spring). 2010;18(12):2395–7. Epub 2010/04/10. doi: 10.1038/oby.2010.88. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 191.Gilbertson NM, Gaitán JM, Osinski V, Rexrode EA, Garmey JC, Mehaffey JH, et al. Pre-operative aerobic exercise on metabolic health and surgical outcomes in patients receiving bariatric surgery: A pilot trial. PLoS One. 2020;15(10):e0239130. Epub 2020/10/03. doi: 10.1371/journal.pone.0239130. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 192.Gilbertson NM, Eichner NZM, Khurshid M, Rexrode EA, Kranz S, Weltman A, et al. Impact of pre-operative aerobic exercise on cardiometabolic health and quality of life in patients undergoing bariatric surgery. Front Physiol. 2020;11:1018. Epub 2020/09/29. doi: 10.3389/fphys.2020.01018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 193.Baillot A, Mampuya WM, Dionne IJ, Comeau E, Méziat-Burdin A, Langlois MF. Impacts of supervised exercise training in addition to interdisciplinary lifestyle management in subjects awaiting bariatric surgery: a randomized controlled study. Obes Surg. 2016;26(11):2602–10. Epub 2016/10/21. doi: 10.1007/s11695-016-2153-9. [DOI] [PubMed] [Google Scholar]
- 194.Berglind D, Willmer M, Eriksson U, Thorell A, Sundbom M, Uddén J, et al. Longitudinal assessment of physical activity in women undergoing Roux-en-Y gastric bypass. Obes Surg. 2015;25(1):119–25. Epub 2014/06/18. doi: 10.1007/s11695-014-1331-x. [DOI] [PubMed] [Google Scholar]
- 195.Coen PM, Tanner CJ, Helbling NL, Dubis GS, Hames KC, Xie H, et al. Clinical trial demonstrates exercise following bariatric surgery improves insulin sensitivity. J Clin Invest. 2015;125(1):248–57. Epub 2014/12/02. doi: 10.1172/JCI78016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 196.Dantas WS, Roschel H, Murai IH, Gil S, Davuluri G, Axelrod CL, et al. Exercise-induced increases in insulin sensitivity after bariatric surgery are mediated by muscle extracellular matrix remodeling. Diabetes. 2020;69(8):1675–91. Epub 2020/05/16. doi: 10.2337/db19-1180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 197.Mundbjerg LH, Stolberg CR, Cecere S, Bladbjerg EM, Funch-Jensen P, Gram B, et al. Supervised physical training improves weight loss after Roux-en-Y gastric bypass surgery: a randomized controlled trial. Obesity (Silver Spring). 2018;26(5):828–37. Epub 2018/03/23. doi: 10.1002/oby.22143.. [DOI] [PubMed] [Google Scholar]
- 198.Dantas W, Gil S, Hisashi Murai I, Costa-Hong V, Peçanha T, Abujabra Merege-Filho C, et al. Reversal of improved endothelial function after bariatric surgery is mitigated by exercise training. Journal of the American College of Cardiology 2018;72:2278–9. [DOI] [PubMed] [Google Scholar]
- 199.Gil S, Pecanha T, Dantas WS, Murai IH, Merege-Filho CAA, de Sa-Pinto AL, et al. Exercise enhances the effect of bariatric surgery in markers of cardiac autonomic function. Obes Surg. 2021;31(3):1381–6. Epub 2020/10/29. doi: 10.1007/s11695-020-05053-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 200.Oppert JM, Bellicha A, Roda C, Bouillot JL, Torcivia A, Clement K, et al. Resistance training and protein supplementation increase strength after bariatric surgery: a randomized controlled trial. Obesity (Silver Spring). 2018;26(11):1709–20. Epub 2018/10/26. doi: 10.1002/oby.22317. [DOI] [PubMed] [Google Scholar]
- 201.Diniz-Sousa F, Veras L, Boppre G, Sa-Couto P, Devezas V, Santos-Sousa H, et al. The effect of an exercise intervention program on bone health after bariatric Surgery: a randomized controlled trial. J Bone Miner Res. 2021;36(3):489–99. Epub 2020/12/10. doi: 10.1002/jbmr.4213. [DOI] [PubMed] [Google Scholar]
- 202.Murai IH, Roschel H, Dantas WS, Gil S, Merege-Filho C, de Cleva R, et al. Exercise mitigates bone loss in women with severe obesity after Roux-en-Y gastric bypass: a randomized controlled trial. J Clin Endocrinol Metab. 2019;104(10):4639–50. Epub 2019/07/20. doi: 10.1210/jc.2019-00074. [DOI] [PubMed] [Google Scholar]
- 203.Coates PS, Fernstrom JD, Fernstrom MH, Schauer PR, Greenspan SL. Gastric bypass surgery for morbid obesity leads to an increase in bone turnover and a decrease in bone mass. J Clin Endocrinol Metab. 2004;89(3):1061–5. Epub 2004/03/06. doi: 10.1210/jc.2003-031756. [DOI] [PubMed] [Google Scholar]
- 204.Yu EW. Bone metabolism after bariatric surgery. J Bone Miner Res. 2014;29(7):1507–18. Epub 2014/03/29. doi: 10.1002/jbmr.2226. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 205.Ott MT, Fanti P, Malluche HH, Ryo UY, Whaley FS, Strodel WE, et al. Biochemical Evidence of metabolic bone disease in women following Roux-Y gastric bypass for morbid Obesity. Obes Surg. 1992;2(4):341–8. Epub 1992/11/01. doi: 10.1381/096089292765559936. [DOI] [PubMed] [Google Scholar]
- 206.Tang MY, Smith DM, Mc Sharry J, Hann M, French DP. Behavior change techniques associated with changes in postintervention and maintained changes in self-efficacy for physical activity: A Systematic Review With Meta-analysis. Ann Behav Med. 2019;53(9):801–15. Epub 2018/12/12. doi: 10.1093/abm/kay090. [DOI] [PubMed] [Google Scholar]
- 207.Takahashi PY, Quigg SM, Croghan IT, Schroeder DR, Ebbert JO. SMART goals setting and biometric changes in obese adults with multimorbidity: Secondary analysis of a randomized controlled trial. SAGE Open Med. 2019;7:2050312119858042. Epub 2019/07/02. doi: 10.1177/2050312119858042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 208.Karmeniemi M, Lankila T, Ikaheimo T, Koivumaa-Honkanen H, Korpelainen R. The built environment as a determinant of physical activity: a systematic review of longitudinal studies and natural experiments. Ann Behav Med. 2018;52(3):239–51. doi: 10.1093/abm/kax043. [DOI] [PubMed] [Google Scholar]
- 209.Morowatisharifabad MA, Abdolkarimi M, Asadpour M, Fathollahi MS, Balaee P. Study on social support for exercise and its impact on the level of physical activity of patients with Type 2 Diabetes. Open Access Maced J Med Sci. 2019;7(1):143–7. Epub 2019/02/12. doi: 10.3889/oamjms.2019.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 210.Schmidt SK, Hemmestad L, MacDonald CS, Langberg H, Valentiner LS. Motivation and barriers to maintaining lifestyle changes in patients with Type 2 Diabetes after an intensive lifestyle intervention (The U-TURN Trial): a longitudinal qualitative study. Int J Environ Res Public Health. 2020;17(20). Epub 2020/10/18. doi: 10.3390/ijerph17207454. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 211.Wycherley TP, Mohr P, Noakes M, Clifton PM, Brinkworth GD. Self-reported facilitators of, and impediments to maintenance of healthy lifestyle behaviours following a supervised research-based lifestyle intervention programme in patients with type 2 diabetes. Diabet Med. 2012;29(5):632–9. Epub 2011/09/16. doi: 10.1111/j.1464-5491.2011.03451.x. [DOI] [PubMed] [Google Scholar]
- 212.Whitfield GP, Carlson SA, Ussery EN, Fulton JE, Galuska DA, Petersen R. Trends in meeting physical activity guidelines among urban and rural dwelling adults - United States, 2008-2017. MMWR Morb Mortal Wkly Rep. 2019;68(23):513–8. Epub 2019/06/14. doi: 10.15585/mmwr.mm6823a1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 213.Hammer NM, Bieler T, Beyer N, Midtgaard J. The impact of self-efficacy on physical activity maintenance in patients with hip osteoarthritis - a mixed methods study. Disabil Rehabil. 2016;38(17):1691–704. Epub 2015/12/19. doi: 10.3109/09638288.2015.1107642. [DOI] [PubMed] [Google Scholar]
- 214.Cerin E, Nathan A, van Cauwenberg J, Barnett DW, Barnett A. The neighbourhood physical environment and active travel in older adults: a systematic review and meta-analysis. Int J Behav Nutr Phys Act. 2017;14(1):15. doi: 0.1186/s12966-017-0471-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 215.den Braver NR, Lakerveld J, Rutters F, Schoonmade LJ, Brug J, Beulens JWJ. Built environmental characteristics and diabetes: a systematic review and meta-analysis. BMC Med. 2018;16(1):12. doi: 0.1186/s12916-017-0997-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 216.Aljasem LI, Peyrot M, Wissow L, Rubin RR. The impact of barriers and self-efficacy on self-care behaviors in type 2 diabetes. Diabetes Educator. 2001;27(3):393–404. Epub 2002/03/27. [DOI] [PubMed] [Google Scholar]
- 217.Dutton GR, Tan F, Provost BC, Sorenson JL, Allen B, Smith D. Relationship between self-efficacy and physical activity among patients with type 2 diabetes. Journal of Behavioral Medicine. 2009;32(3):270–7. Epub 2009/01/22. doi: 10.1007/s10865-009-9200-0. [DOI] [PubMed] [Google Scholar]
- 218.McAuley E, Blissmer B. Self-efficacy determinants and consequences of physical activity. Exerc Sport Sci Rev. 2000;28(2):85–8. [PubMed] [Google Scholar]
- 219.Armit CM, Brown WJ, Marshall AL, Ritchie CB, Trost SG, Green A, et al. Randomized trial of three strategies to promote physical activity in general practice. Preventive Medicine. 2009;48(2):156–63. Epub 2008/12/23. doi: S0091-7435(08)00620-8 [pii] 10.1016/j.ypmed.2008.11.009. [DOI] [PubMed] [Google Scholar]
- 220.Balducci S, Zanuso S, Fernando F, Nicolucci A, Cardelli P, Cavallo S, et al. The Italian diabetes and exercise study. Diabetes. 2008;57(Suppl. 1):A306–A7. [Google Scholar]
- 221.Statistics NCfH. Health, United States, 2018. Hyattsville, MD: 2019. [Google Scholar]
- 222.Saffer H, Dave D, Grossman M, Leung LA. Racial, ethnic, and gender differences in physical activity. J Hum Cap. 2013;7(4):378–410. Epub 2013/01/01. doi: 10.1086/671200. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 223.Moore LV, Harris CD, Carlson SA, Kruger J, Fulton JE. Trends in no leisure-time physical activity--United States, 1988–2010. Res Q Exerc Sport. 2012;83(4):587–91. Epub 2013/02/02. doi: 10.1080/02701367.2012.10599884. [DOI] [PubMed] [Google Scholar]
- 224.QuickStats: Percentage of Adults Who Met Federal Guidelines for Aerobic Physical Activity Through Leisure-Time Activity,* by Race/Ethnicity - National Health Interview Survey,(†) 2008-2017. MMWR Morb Mortal Wkly Rep. 2019;68(12):292. Epub 2019/03/29. doi: 10.15585/mmwr.mm6812a6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 225.Gray CL, Messer LC, Rappazzo KM, Jagai JS, Grabich SC, Lobdell DT. The association between physical inactivity and obesity is modified by five domains of environmental quality in U.S. adults: A cross-sectional study. PLoS One. 2018;13(8):e0203301. Epub 2018/08/31. doi: 10.1371/journal.pone.0203301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 226.Hawes AM, Smith GS, McGinty E, Bell C, Bower K, LaVeist TA, et al. Disentangling race, poverty, and place in disparities in physical activity. Int J Environ Res Public Health. 2019;16(7). Epub 2019/04/17. doi: 10.3390/ijerph16071193. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 227.Chien LC, Li X, Staudt A. Physical inactivity displays a mediator role in the association of diabetes and poverty: A spatiotemporal analysis. Geospat Health. 2017;12(2):528. Epub 2017/12/15. doi: 10.4081/gh.2017.528. . [DOI] [PubMed] [Google Scholar]
- 228.Hunter RF, Christian H, Veitch J, Astell-Burt T, Hipp JA, Schipperijn J. The impact of interventions to promote physical activity in urban green space: a systematic review and recommendations for future research. Soc Sci Med. 2015;124:246–56. Epub 2014/12/03. doi: 10.1016/j.socscimed.2014.11.051. [DOI] [PubMed] [Google Scholar]
- 229.Kershaw KN, Pender AE. Racial/ethnic residential segregation, obesity, and diabetes mellitus. Current diabetes reports. 2016;16(11):108. Epub 2016/09/25. doi: 10.1007/s11892-016-0800-0. [DOI] [PubMed] [Google Scholar]
- 230.Kuo M How might contact with nature promote human health? Promising mechanisms and a possible central pathway. Front Psychol. 2015;6:1093. Epub 2015/09/18. doi: 10.3389/fpsyg.2015.01093. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 231.Prevention CfDCa. Status Report for Step It Up! The Surgeon General’s Call to Action to Promote Walking and Walkable Communities. US Dept of Health and Human Services; 2017. [Google Scholar]
- 232.Thornton PL, Kumanyika SK, Gregg EW, Araneta MR, Baskin ML, Chin MH, et al. New research directions on disparities in obesity and type 2 diabetes. Annals of the New York Academy of Sciences. 2020;1461(1):5–24. Epub 2019/12/04. doi: 10.1111/nyas.14270. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 233.Drewnowski A, Arterburn D, Zane J, Aggarwal A, Gupta S, Hurvitz PM, et al. The Moving to Health (M2H) approach to natural experiment research: A paradigm shift for studies on built environment and health. SSM Popul Health. 2019;7:100345. Epub 2019/01/19. doi: 10.1016/j.ssmph.2018.100345. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 234.Auchincloss AH, Diez Roux AV, Mujahid MS, Shen M, Bertoni AG, Carnethon MR. Neighborhood resources for physical activity and healthy foods and incidence of type 2 diabetes mellitus: the Multi-Ethnic study of Atherosclerosis. Arch Intern Med. 2009;169(18):1698–704. Epub 2009/10/14. doi: 10.1001/archinternmed.2009.302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 235.Ludwig J, Sanbonmatsu L, Gennetian L, Adam E, Duncan GJ, Katz LF, et al. Neighborhoods, obesity, and diabetes--a randomized social experiment. N Engl J Med. 2011;365(16):1509–19. Epub 2011/10/21. doi: 10.1056/NEJMsa1103216. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 236.Diabetes Canada. The Built Environment and Diabetes: A Position Statement. Ottawa, 2020. https://www.diabetes.ca/advocacy---policies/our-policy-positions/the-built-environment-and-diabetes [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.