Abstract
Background
There are few data on the prevalence of obesity and its influence on achieving blood glucose, blood pressure, and blood lipid (3B) goals in Chinese type 2 diabetes outpatients.
Methods
Patient demographic data, anthropometric measurements, medications, and blood glucose and lipid profiles of 24,512 type 2 diabetes patients from a large, geographically diverse study (CCMR-3B) were analyzed. Using cut-points for body mass index (BMI) and waist circumference (WC) recommended by the Working Group on Obesity in China, overweight and obesity were defined as BMIs of 24–27.9kg/m2 and ≥28.0kg/m2. Central obesity was defined as a waist circumference ≥80cm in women and ≥85cm in men. The 3B therapeutic goals were HbA1c<7.0%, BP<140/90mmHg and LDL-C<2.6mmol/L.
Results
Overall, 43.0% of type 2 diabetes patients were overweight and 16.7% were obese; 13.3% of overweight and and10.1% of obese patients achieved all the 3B target goals. Overweight or obese patients were less likely to achieve 3B goals than those with normal BMIs. More than a half the overweight or obese patients (69.6%) were centrally obese. Patients with abdominal obesity were less likely to achieve cardiometabolic targets than those without abdominal obesity. In multivariate logistic regression analysis, female, higher BMI and waist circumference, smoking, drinking, sedentary lifestyle, and longer diabetes duration were significantly correlated with failure to achieve 3B control goals.
Conclusions
Obesity is highly prevalent and associated with poor 3B control in Chinese type 2 diabetes patients. In clinical practice, more attention and resources should focus on weight loss for such patients.
Introduction
The global prevalence of diabetes is rapidly increasing, and in China, the estimated prevalence of type 2 diabetes in adults rose from 2.5% in 1994 to 9.7% in 2007–2008 [1, 2]. There is strong evidence from epidemiological studies showing that obese diabetes patients are at increased risk of cardiometabolic diseases including hyperglycemia, hypertension, and dyslipidemia [3–6]. A meta-analysis of five longitudinal cohort studies demonstrated that overweight or obese diabetes patients had a twofold greater relative risk of mortality than normal-weight patients[7]. However, currently no studies have directly compared the rates of achieving therapeutic goals for control of hyperglycemia, hypertension, and dyslipidemia in normal weight and obese patients with diabetes who had been receiving medical care in hospital setting.
Cardiovascular events contribute to morbidity and mortality from diabetes, but control of cardiometabolic risk factors among diabetes patients is reported to be poor [8]. Identification of the factors that contribute to poor control would help to reduce morbidity and mortality in these patients. Overweight and obesity are characterized by excessive body fat accumulation that impairs both physical and psychosocial health. General obesity, i.e., overall body fat, is usually estimated by the body mass index (BMI), and waist circumference (WC), which measures abdominal fat, is the easiest way to assess central obesity. A survey of 233 type 2 diabetes patients, found that control of hyperglycemia, hypertension, and dyslipidemia was poor in 65.7%, 51.9%, and 97.1% of the subjects respectively, and that 60.1% of them were either overweight or obese [8]. Study supports the combined use of general and central obesity, as measured by BMI and WC, to assess risk of cardiovascular diseases in patients with diabetes and metabolic disorders [9].
Current type 2 diabetes treatment guidelines recommend multifactorial intervention, including both lifestyle modification and pharmacologic treatment [10,11]. However, even with multifactorial interventions, it is not known if diabetes patients with different BMIs have similar success in achieving recommended target goals for control of hyperglycemia, hypertension, and dyslipidemia in a real-life setting. We evaluated a population of overweight and obese patients from the Nationwide Assessment of Cardiovascular Risk Factors: Blood Glucose, Blood Pressure, and Blood Lipid (3B) study, a large, cross-sectional investigation of Chinese patients with type 2 diabetes [12]. We aimed to assess the achievement of 3B goals in this population and to compare the proportions of patients with different BMIs who achieved the target therapeutic goals set by the parent study. The influence of lifestyle on achieving the 3B targeted goals was assessed.
Materials and Methods
Study design and participants
The 3B study was conducted from August 2010 to March 2011 in endocrinology, cardiology, nephrology, and internal medicine clinics in 104 hospitals across all major geographic regions in China (registered in clinicaltrials.gov, NCT01128205). The study design and population have been described previously [12]. Briefly, it was a purely observational study, as only available data were documented, and patient treatment or assessment was not changed by the study. Endocrinology, cardiology, nephrology, and internal medicine specialists conducted the study. Consecutive outpatients were eligible for inclusion if they were 18 years of age or older and were diagnosed with type 2 diabetes at least 6 months prior to study screening. The study protocol was approved by the Ethics Committees of Peking University People’s Hospital, China–Japan Friendship Hospital, The Third Affiliated Hospital of Sun Yat-sen University, Huashan Hospital Fudan University, Shanghai Changzhen Hospital, Jiangsu Province Hospital, and The Second Affiliated Hospital of Dalian Medical University. All patients provided written informed consent to participate. Of 25,454 eligible patients, 610 with a BMI <18.5 kg/m2, and 23 with missing data, including BMI, hemoglobin A1c (HbA1c), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), or triglycerides (TG), were excluded. An additional 309 participants with extreme values (i.e., below the 0.1 percentile or above the 99.9 percentile) of age, BMI, duration of diabetes, LDL-C, TC, HDL-C, TG, and HbA1c were excluded. The remaining 24,512 patients (11,543 men and 12,969 women) were included in this study.
Data collection
Patient data were collected from medical charts and clinical examinations conducted at one outpatient visit. Information on health behavior (i.e., smoking status, alcohol consumption, and exercise intensity), current medications, and personal history of hypertension and major cardiovascular diseases were obtained by self-reporting during a face-to-face interview. Physical examination included anthropometry and blood pressure measurements; height and weight were measured with patients standing with bare feet and light clothing on a mechanical balance. Fasting serum glucose, TC, LDL-C, HDL-C, and TG were measured at each study site with an automated analyzer. An HbA1c concentration known to have been obtained during the 3 months prior to the enrollment visit, or obtained at enrollment, was recorded.
Definitions of variables
Smoking was defined as consuming an average of at least one cigarette daily for at least 1 year. Drinking was defined as consuming an average at least 50 g of alcohol daily for at least 1 year. A sedentary lifestyle was defined as not participating in regular physical activities.
BMI was calculated as weight in kilograms divided by the square of height in meters (kg/m2). As recommended by the Working Group on Obesity in China, normal weight was defined as a BMI of 18.5–23.9 kg/m2, overweight as a BMI of 24.0–27.9, and obesity as a BMI of 28.0 kg/m2 or higher [13–15]. A normal WC was defined as <80cm in women and <85 cm in men; WCs ≥80cm in women and ≥85cm in men indicated central obesity [13].
Each patient was evaluated for attainment of 3B study therapeutic control goals. According to the China Guidelines for Type 2 Diabetes (2013) and the American Diabetes Association recommendations (2015) [16,17], attainment of the glycemic goal was defined as an HbA1c <7%, the blood pressure (BP) goal was a systolic blood pressure (SBP) <140mmHg and a diastolic blood pressure (DBP) <90mmHg regardless of a history of hypertension or current antihypertensive treatment. The LDL-C goal was <2.6mmol/l regardless of a history of dyslipidemia or current anti-hyperlipidemia treatment.
Statistical analysis
Statistical analysis was performed using SAS version 9.2 (SAS Institute Inc., Cary, NC, USA). Quantitative variables were expressed as means±standard deviation (SD) or medians and percentiles (25th percentile, 75th percentile). Categorical variables were reported as numbers and percentages. Between-group differences of continuous variables were tested for significance using one-way analysis of variance (ANOVA), and the chi-square or Fisher’s exact test were used for categorical data. Logistic regression analysis was used to determine the independent association between attainment of 3B therapeutic goals and the variables of age, gender, smoking status, alcohol consumption, sedentary lifestyle, BMI, WC, diabetes duration, and diabetes complications. Backward elimination (= 0.05) was performed. The results were expressed as odds ratios (ORs) with 95% confidence intervals (CIs). Statistical significance was accepted as a two-sided test with an alpha level of 0.05.
Results
Demographic and clinical characteristics
The demographic and clinical characteristics of the 24,512 patients with type 2 diabetes were stratified by BMI and WC and are shown in Table 1. The prevalence of overweight was 43.0% (n = 10,548), and 16.7% (n = 4098) of the patients were obese; 11,543 (47.1%) were men and 12,969 (52.9%) were women. The mean age of normal-weight diabetes patients was 63.5±11.6years, overweight patients were 62.2±11.7years of age, and obese patients were 60.8±12.4years of age (P<0.001). Obese patients had a shorter diabetes duration than normal-weight patients, but were more likely to have comorbidities (hypertension or hypertension with dyslipidemia). Alcohol consumption and sedentary lifestyle were more common in obese than in normal-weight patients. A greater percentage of overweight and obese patients had diabetes complications, including cardiovascular diseases, cerebrovascular disease, and nephropathy, compared with normal-weight patients (all P<0.05).
Table 1. Demographic and clinical characteristics of diabetes patients stratified by BMI and WC.
Total(n = 24,512) | BMI (kg/m2) | BMI ≥24kg/m2 | ||||||
---|---|---|---|---|---|---|---|---|
<24(n = 9866) | 24–27.9(n = 10,548) | ≥28(n = 4098) | P | Normal WC(n = 2904) | Central obesity(n = 6642) | P | ||
Age, years (mean±SD) | 62.5±11.8 | 63.5±11.6 | 62.2±11.7 | 60.8±12.4 | <0.001 | 62.0±11.8 | 60.6±12.1 | <0.001 |
<45 | 1697 (6.9) | 576 (5.8) | 717 (6.8) | 404 (9.9) | <0.001 | 202 (7.0) | 631 (9.5) | <0.001 |
45–54 | 4408 (18.0) | 1615 (16.4) | 1968 (18.7) | 825 (20.1) | 572 (19.7) | 1386 (20.9) | ||
55–64 | 7323 (29.9) | 2856 (28.9) | 3263 (30.9) | 1204 (29.4) | 888 (30.6) | 2032 (30.6) | ||
≥65 | 11084 (45.2) | 4819 (48.8) | 4600 (43.6) | 1665 (40.6) | 1242 (42.8) | 2593 (39.0) | ||
Male | 11543 (47.1) | 4524 (45.9) | 5291 (50.2) | 1728 (42.2) | <0.001 | 1345 (46.3) | 4614 (69.5) | <0.001 |
Diabetes duration, years, median (25th, 75th percentile) | 6.2 (2.7, 11.3) | 6.7 (2.7, 12.0) | 6.0 (2.7,11.0) | 5.9 (2.5, 10.9) | <0.001 | 6.0 (2.6, 11.0) | 5.7 (2.4, 10.8) | 0.001 |
<1 | 2210 (9.0) | 897 (9.1) | 950 (9.0) | 363 (8.9) | <0.001 | 265 (9.1) | 653 (9.8) | 0.002 |
1–4 | 8135 (33.2) | 3101 (31.4) | 3578 (33.9) | 1456 (35.5) | 967 (33.3) | 2399 (36.12) | ||
5–9 | 5878 (24.0) | 2289 (23.2) | 2579 (24.5) | 1010 (24.6) | 704 (24.2) | 1622 (24.42) | ||
≥10 | 8289 (33.8) | 3579 (36.3) | 3441 (32.6) | 1269 (31.0) | 968 (33.3) | 1968 (29.6) | ||
Comorbidities* | 17756 (72.4) | 6447 (65.3) | 7931 (75.2) | 3378 (82.4) | <0.001 | 2084 (71.8) | 5079 (76.5) | <0.001 |
Hypertension | 7367 (30.1) | 2926 (29.7) | 3150 (29.9) | 1291 (31.5) | 866 (29.8) | 1942 (29.2) | ||
Dyslipidemia | 3018 (12.3) | 1156 (11.7) | 1404 (13.3) | 458 (11.2) | 351 (12.1) | 973 (14.7) | ||
Hypertension and Dyslipidemia | 7371 (30.1) | 2365 (24.0) | 3377 (32.0) | 1629 (39.8) | 867 (29.9) | 2164 (32.6) | ||
Smoking | 4052 (16.5) | 1433 (14.5) | 1921 (18.2) | 698 (17.0) | <0.001 | 471 (16.2) | 1669 (25.1) | <0.001 |
Alcohol consumption | 1959 (8.0) | 607 (6.2) | 958 (9.1) | 394 (9.6) | <0.001 | 227 (7.8) | 876 (13.2) | <0.001 |
Sedentary lifestyle | 8824 (36.0) | 3403 (34.5) | 3692 (35.0) | 1729 (42.2) | <0.001 | 1031 (35.5) | 2313 (34.8) | 0.522 |
Diabetes complications | ||||||||
Cardiovascular diseases | 3653 (14.9) | 1266 (12.8) | 1663 (15.8) | 724 (17.7) | <0.001 | 458 (15.8) | 1004 (15.1) | 0.413 |
Cerebrovascular disease | 2469 (10.1) | 981 (9.9) | 1061 (10.1) | 427 (10.4) | 0.694 | 245 (8.4) | 653 (9.8) | 0.032 |
Peripheral vascular diseases | 370 (1.5) | 161 (1.6) | 132 (1.3) | 77 (1.9) | 0.009 | 31 (1.1) | 85 (1.3) | 0.384 |
Nephropathy | 3525 (14.4) | 1271 (12.9) | 1540 (14.6) | 714 (17.4) | <0.001 | 377 (13.0) | 1021 (15.4) | 0.002 |
Retinopathy | 4018 (16.4) | 1698 (17.2) | 1645 (15.6) | 675 (16.5) | 0.008 | 409 (14.1) | 891 (13.4) | 0.380 |
Neuropathy | 3702 (15.1) | 1486 (15.1) | 1545 (14.6) | 671 (16.4) | 0.032 | 387 (13.3) | 933 (14.1) | 0.348 |
Data are expressed as n (%) unless otherwise indicated.
* Comorbidities included hypertension only, dyslipidemia only, and both conditions.
Of the 9546 overweight patients with a BMI ≥24kg/m2 (excluding 5,100 patients with missing WC data), 6642 (69.6%) were centrally obese; and of those, 69.5% were men. A significantly larger percentage of patients with central obesity had comorbidities compared with those who had a normal WC (76.5% vs. 71.8%, P<0.001). Centrally obese patients were also more likely to be smokers or alcohol drinkers (P<0.001).
Medication regimens
The numbers and percentages of patients receiving pharmaceutical treatment for diabetes, hypertension, and dyslipidemia are shown in Table 2. The most frequently reported oral antidiabetic agents were metformin (38.6%), followed by sulfonylureas (28.9%) and -glucosidase inhibitors (26.6%). Use of antihypertensive, lipid lowering and oral antidiabetic agents was most frequent in obese patients. More than half of the obese patients (52.3%) were taking antihypertensive agents, and more than a quarter (27.9%) were taking blood-lipid lowering agents, compared with 37.6% and 19.8% of normal-weight patients, respectively (P<0.001). More centrally obese patients than patients with a normal WC were taking antihypertensive and oral antidiabetic agents (P<0.001). Interestingly, insulin treatment did not vary among patients with different BMI.
Table 2. Medication regimens of diabetes patients stratified by BMI and WC.
BMI (kg/m2) | BMI ≥24kg/m2 | |||||||
---|---|---|---|---|---|---|---|---|
Total(n = 24,512) | <24(n = 9866) | 24–27.9(n = 10,548) | ≥28(n = 4098) | P | Normal WC(n = 2904) | Central obesity(n = 6642) | P | |
Antihypertensive agents | 10577 (43.2) | 3711 (37.6) | 4722 (44.8) | 2144 (52.3) | <0.001 | 1244 (42.8) | 2965 (44.6) | <0.001 |
Lipid lowering agents | 5776 (23.6) | 1954 (19.8) | 2679 (25.4) | 1143 (27.9) | <0.001 | 715 (24.6) | 1727 (26.0) | 0.473 |
Oral anti-diabetic agents | 17992 (73.4) | 7140 (72.4) | 7753 (73.5) | 3099 (75.6) | <0.001 | 2019 (69.5) | 4919 (74.1) | <0.001 |
Metformin | 9460 (38.6) | 3314 (33.6) | 4216 (40.0) | 1930 (47.1) | <0.001 | 1064 (36.6) | 2774 (41.8) | 0.131 |
α-glucosidase inhibitors | 6527 (26.6) | 2664 (27.0) | 2774 (26.3) | 1089 (26.6) | 0.031 | 696 (24.0) | 1735 (261.) | 0.424 |
Sulfonylureas | 7075 (28.9) | 3038 (30.8) | 3016 (28.6) | 1021 (24.9) | <0.001 | 752 (25.9) | 1816 (27.3) | 0.664 |
Thiazolidinediones | 1820 (7.4) | 677 (6.9) | 782 (7.4) | 361 (8.8) | 0.289 | 159 (5.5) | 530 (8.0) | 0.098 |
Insulin | 8688 (35.4) | 3414 (34.6) | 3788 (35.9) | 1486 (36.3) | 0.072 | 1077 (37.1) | 2334 (35.1) | 0.068 |
Data are expressed as n (%)
Control of blood glucose, blood pressure and blood lipids
The 3B profiles and goal-attainment rates of the study patients are shown in Table 3. Overweight and obese patients had higher SBP, DBP, and fasting serum glucose, HbA1c, TC, LDL-C and TG, but lower HDL-C levels than normal-weight patients (P<0.05). Centrally obese patients had higher HbA1c and TG levels, but lower HDL-C levels than did patients with a normal WC (P<0.05).
Table 3. 3B profiles and goal attainment rates of diabetes patients stratified by BMI and WC.
BMI (kg/m2) | BMI ≥24 kg/m2 | |||||||
---|---|---|---|---|---|---|---|---|
Total(n = 24,512) | <24(n = 9866) | 24–27.9(n = 10,548) | ≥28(n = 4098) | P | Normal WC(n = 2904) | Central obesity(n = 6642) | P | |
SBP (mmHg) | 133.1±15.7 | 131.2±15.4 | 133.8±15.5 | 135.9±16.1 | <0.001 | 133.4±15.5 | 133.5±15.4 | 0.797 |
DBP (mmHg) | 78.9±8.9 | 77.3±8.5 | 79.4±8.8 | 81.4±9.5 | <0.001 | 79.7±9.0 | 80.0±9.0 | 0.088 |
FPG (mmol/L) | 8.4±3.4 | 8.3±3.5 | 8.4±3.3 | 8.6±3.3 | <0.001 | 8.4±3.5 | 8.4±3.2 | 0.849 |
HbA1c (%) | 7.6±2.0 | 7.5±2.1 | 7.6±1.9 | 7.8±1.9 | <0.001 | 7.5±2.0 | 7.7±1.9 | 0.003 |
TC (mmol/L) | 4.97±1.21 | 4.95±1.22 | 4.97±1.20 | 5.01±1.21 | 0.015 | 5.01±1.24 | 4.92±1.18 | 0.092 |
LDL-C (mmol/L) | 2.84±0.91 | 2.82±0.90 | 2.95±0.91 | 2.86±0.92 | 0.014 | 2.84±0.92 | 2.83±0.90 | 0.570 |
HDL-C (mmol/L) | 1.30±0.43 | 1.35±0.44 | 1.27±0.42 | 1.26±0.44 | <0.001 | 1.29±0.45 | 1.24±0.41 | <0.001 |
TG (mmol/L) | 1.98±1.65 | 1.76±1.42 | 2.09±1.75 | 2.25±1.80 | <0.001 | 2.03±1.49 | 2.17±1.93 | <0.001 |
HbA1c <7.0% | 11,000 (44.9) | 4793 (48.6) | 4623 (43.8) | 1584 (38.7) | <0.001 | 1341 (46.2) | 2834 (42.7) | 0.001 |
BP <140/90 mmHg | 9885 (40.3) | 4655 (47.2) | 4000 (37.9) | 1230 (30.0) | <0.001 | 1930 (66.5) | 4313 (64.9) | 0.150 |
LDL-C <2.6 mmol/L | 10,426 (42.5) | 4287 (43.5) | 4427 (42.0) | 1712 (41.8) | 0.057 | 1254 (43.2) | 2858 (43.0) | 0.890 |
3B at goal | 3512 (14.3) | 1696 (17.2) | 1401 (13.3) | 415 (10.1) | <0.001 | 426 (14.7) | 853 (12.8) | 0.016 |
FPG, fasting plasma glucose. *3B goal was BP<140/90mmHg, LDL-C<2.6mmol/L, and HbA1c<7.0%. Data are shown as means±SD or n (%).
A total of 44.9% of the patients reached the recommended glycemic control target (HbA1c <7%); 40.3% achieved the BP target (<140/90mmHg), and 42.5% reached the lipid control target (LDL-C <2.6mmol/L). All 3B target goals (i.e., control of HbA1c, BP, and LDL-C) were achieved by 14.3% of the study participants. A total of 48.6% of normal-weight patients achieved HbA1c control, 47.2% achieved BP control, and 17.2% achieved all the 3B target goals compared with 38.7%, 30.0% and 10.1% of obese patients, respectively (P<0.001). A similar trend was seen in centrally obese patients, suggesting that patients who had an abnormal BMI and an abnormal WC were at increased risk of failure to achieve target therapeutic goals.
Risk factors that influence the 3B control
Logistic regression analysis showed (Table 4) that higher BMI (OR = 1.26; 95%CI, 1.15–1.38 for BMI = 24–27.9kg/m2 and OR = 1.62; 95%CI, 1.37–1.93 for BMI ≥28 kg/m2), higher WC (OR = 1.01; 95%CI, 1.01–1.02), smoking (OR = 1.38; 95%CI, 1.22–1.57), drinking (OR = 1.31; 95%CI, 1.10–1.55), and longer diabetic duration (OR = 1.69; 95%CI, 1.46–1.95 for 5–9 years and OR = 1.45; 95% CI, 1.25–1.68 for ≥10 years) made it less likely to achieve 3B control goals. Male patients (OR = 0.78; 95%CI, 0.71–0.86) and frequent exercisers (OR = 0.85; 95%CI, 0.78–0.93) were more likely to achieve all 3B control targets.
Table 4. Factors associated with failure to achieve 3B goals by logistic regression analysis.
Variables | BP <140/90mmHg | LDL-C <2.6mmol/L | HbA1c <7.0% | 3B at goal | ||||
---|---|---|---|---|---|---|---|---|
OR (95% CI) | P | OR (95% CI) | P | OR (95% CI) | P | OR (95% CI) | P | |
Age (years), vs. <45years | ||||||||
45–54 | 1.63 (1.39, 1.91) | <0.001 | 1.02 (0.90, 1.16) | 0.727 | 0.76 (0.66, 0.87) | <0.001 | 1.05 (0.88, 1.25) | 0.611 |
55–64 | 1.89 (1.62, 2.20) | <0.001 | 1.15 (1.02, 1.31) | 0.022 | 0.56 (0.50, 0.64) | <0.001 | 1.03 (0.87, 1.23) | 0.699 |
≥65 | 2.29 (1.96, 2.66) | <0.001 | 0.94 (0.83, 1.07) | 0.340 | 0.48 (0.43, 0.55) | <0.001 | 0.85 (0.72, 1.01) | 0.060 |
Gender (male vs. female) | 0.98 (0.91, 1.06) | 0.616 | 0.67 (0.62, 0.72) | <0.001 | 0.97 (0.90, 1.04) | 0.350 | 0.78 (0.71, 0.86) | <0.001 |
Smoking (yes vs. no) | 1.00 (0.91, 1.10) | 0.991 | 1.12 (1.02, 1.22) | 0.012 | 1.41 (1.29, 1.54) | <0.001 | 1.38 (1.22, 1.57) | <0.001 |
Drinking (yes vs. no) | 1.18 (1.05, 1.33) | 0.006 | 1.11 (0.99, 1.24) | 0.067 | 1.15 (1.03, 1.29) | 0.016 | 1.31 (1.10, 1.55) | 0.002 |
Exercise (yes vs. no) | 0.87 (0.82, 0.94) | <0.001 | 0.99 (0.93, 1.04) | 0.653 | 0.77 (0.72, 0.82) | <0.001 | 0.85 (0.78, 0.93) | <0.001 |
BMI (kg/m2) vs. <24kg/m2 | ||||||||
24–27.9 | 1.30 (1.21, 1.40) | <0.001 | 1.04 (0.97, 1.11) | 0.298 | 1.11 (1.04, 1.19) | 0.002 | 1.26 (1.15, 1.38) | <0.001 |
≥28 | 1.66 (1.48, 1.87) | <0.001 | 1.03 (0.92, 1.16) | 0.567 | 1.25 (1.11, 1.4) | <0.001 | 1.62 (1.37, 1.93) | <0.001 |
Abnormal WC vs. normal WC | 1.01 (1.00, 1.01) | <0.001 | 1.01 (1.00, 1.01) | 0.002 | 1.01 (1.01, 1.02) | <0.001 | 1.01 (1.01, 1.02) | <0.001 |
Diabetes duration (years), vs. <1year | ||||||||
1–4 | 1.05 (0.93, 1.18) | 0.466 | 1.00 (0.89, 1.11) | 0.931 | 0.95 (0.85, 1.06) | 0.383 | 1.06 (0.92, 1.21) | 0.415 |
5–9 | 1.25 (1.11, 1.42) | <0.001 | 0.99 (0.88, 1.10) | 0.813 | 1.99 (1.77, 2.22) | <0.001 | 1.69 (1.46, 1.95) | <0.001 |
≥10 | 1.11 (0.98, 1.26) | 0.106 | 1.02 (0.91, 1.15) | 0.682 | 1.44 (1.28, 1.61) | <0.001 | 1.45 (1.25, 1.68) | <0.001 |
Diabetes complications (yes vs. no) | ||||||||
Cardiovascular | 1.18 (1.08, 1.29) | <0.001 | 0.70(0.64, 0.77) | <0.001 | 0.93 (0.85, 1.01) | 0.093 | 0.82 (0.73, 0.92) | <0.001 |
Cerebrovascular | 1.37 (1.23, 1.52) | <0.001 | 0.93 (0.84, 1.02) | 0.133 | 1.05 (0.95, 1.17) | 0.350 | 1.15 (1.00, 1.34) | 0.057 |
Peripheral | 1.47 (1.14, 1.89) | 0.003 | 0.96 (0.75, 1.23) | 0.737 | 1.20 (0.92, 1.56) | 0.178 | 1.53 (0.99, 2.37) | 0.055 |
Nephropathy | 1.68 (1.54, 1.84) | <0.001 | 0.96 (0.88, 1.04) | 0.312 | 1.05 (0.96, 1.15) | 0.258 | 1.40 (1.22, 1.60) | <0.001 |
Retinopathy | 1.18 (1.08, 1.29) | <0.001 | 1.05 (0.96, 1.15) | 0.258 | 0.96 (0.88, 1.05) | 0.385 | 1.07 (0.94, 1.20) | 0.305 |
Neuropathy | 1.13 (1.03, 1.24) | 0.009 | 1.06 (0.97 1.15) | 0.211 | 1.47 (1.34, 1.61) | <0.001 | 1.29 (1.13, 1.47) | <0.001 |
Discussion
Although the attainment of integrated glycemic, blood pressure and lipid goal is recommended by the current diabetes treatment guidelines, a smaller percentage of obese or overweight diabetes patients were able to achieve 3B goals compared with normal-weight patients. Furthermore, we observed that central obesity was significantly correlated with failure to achieve the 3B goal. To our knowledge, the present analysis is a first study to systematically assess the effect of obesity on 3B control in a large, geographically diverse sample of patients with type 2 diabetes. Given the upward trajectory in prevalence of obesity in diabetes, our findings clearly illustrate the importance of weight control for improving the 3B control rate and reducing the disease burden.
The health consequences of diabetes are compounded by overweight and obesity. In this study, 43.0% of diabetes patients were overweight and 16.7% were obese. In fact, we overestimated overweight and obesity based on the Chinese-specific BMI cutoffs of 24 and 28kg/m2 relative to the WHO criteria of 25 and 30kg/m2. Therefore, we recalculated the prevalence of overweight and obesity in this Chinese population using the WHO criteria, which gave prevalences of 38.77% (9503/24 512) for overweight and 7.14% (1750/24 512) for obesity in our study population. These rates are considerably lower than the percentages reported in a survey conducted in the United States in 1999–2002 [18]. In that survey, the combined prevalence of overweight and obesity (BMI ≥25kg/m2) was 85.2%, and the prevalence of obesity (BMI ≥30kg/m2) was 54.8%. A systematic literature review found a high variability in the prevalence of obesity in type 2 diabetes patients living in different countries [19]. Given the differences of ethnicities, country specified obesity criteria (e.g., BMI, WC, and waist/hip ratio) and obesity thresholds should be adapt for the country.
Hyperglycemia, hypertension, and dyslipidemia occur frequently in type 2 diabetes patients [19,20]. Iwahashi et al. reported that after oral glucose loading, insulin levels were higher in obese than in non-obese type 2 diabetes patients [21]. Obese (BMI ≥30kg/m2) type 2 diabetes patients treated at a clinic in the UK had higher blood pressure and triglyceride levels than nonobese patients, and that total cholesterol and glycemic control were worse in obese than nonobese male patients [22]. Similarly, our study found that overweight or obesity was associated with increased likelihood of comorbid hypertension and/or dyslipidemia. Overweight and obese patients also had higher SBP, DBP, fasting serum glucose, HbA1c, TC, LDL-C, and TG, but lower HDL-C levels than normal-weight patients. We also found that comorbidities occurred more often in overweight patients with central obesity than in those with a normal WC. Overall, these findings are in line with the Look AHEAD (Action for Health in Diabetes) study, a long-term trial of lifestyle intervention for weight loss that reported weight loss improved glycemic control, blood pressure, and lipid profiles in overweight type 2 diabetes patients [23].
In this study, the most frequently used oral antidiabetic agents were metformin (38.6%), sulfonylureas (28.9%), and α-glucosidase inhibitors (26.6%). A clinical trial conducted in Chinese patients with newly diagnosed type 2 diabetes reported no differences in the efficacy of metformin monotherapy to reduce HbA1c and LDL-C levels in normal weight, overweight, or obese patients after 16 weeks of treatment [24]. Another observational study reported similar reductions of glycaemia in patients with different BMIs after insulin detemir was added to treatment regimens that included oral glucose lowering drugs [25]. In this study, obese patients had higher average levels of TC, TG, and HbA1c, than other patients, but antihypertensive, lipid lowering and oral antidiabetic agents were used more frequently in obese than in other patients. This suggests that obese patients might require more complex pharmacological therapy to modify their cardiovascular risk factors.
Overall, only 14.3% of the enrolled patients achieved all 3B target goals. The proportion of 3B-controled patients decreased in overweight and obese patients, with only 10.1% of obese patients achieving all three therapeutic targets. Our findings confirm the negative impact of obesity on achieving 3B treatment goals, and that the negative effects were not offset by pharmacotherapy, emphasizing the known benefit of weight loss in diabetes patients [26,27]. The occurrence of hypertension, diabetes, and hyperlipidemia along with obesity has been referred to as a cardiometabolic risk factor cluster (CMRFC) [28]. More than 80% of the diabetes patients in this study had one or more concomitant cardiovascular risk factor, which made the choice of a treatment regimen complex and presented a significant challenge to effective achievement of 3B targets. The logistic regression analysis found that a BMI ≥24kg/m2 and an abnormal WC predicted failure to achieve the 3B therapeutic goals. Interestingly, our logistic regression results indicated that BMI seemed to be a stronger predictor than waist circumference. Determining this with certainty, however, will require long-term follow-up and further investigation.
Lifestyle can influence achievement of therapeutic goals for control of hyperglycemia, hypertension, and dyslipidemia in diabetic patients. In this study, alcohol consumption and a sedentary lifestyle were reported by more obese than normal weight patients. Frequent exercise might be of benefit in achieving 3B control. Qin et al. proposed that obesity and physical activity have an additive impact, and that prevention of either obesity or physical inactivity effectively reduces the risks of diabetes and its comorbid cardiometabolic diseases [29]. Physical activity may increase insulin sensitivity, glucose disposal, and oxidation of free fatty acids [29]. Moreover, the benefits of physical activity may extend beyond weight loss alone to include reduction of systemic and vascular inflammation [30]. Thus, 150 min/week of regular physical activity has been recommended as an intervention in diabetes treatment [10]. However, some studies have found that exercise had no measurable effect on glucose regulation in obese individuals without concomitant weight loss, and that the beneficial effect of exercise on metabolic complications seems only achievable when accompanied by weight loss [29]. In this study, smoking and drinking appeared to be independent risk factors for the failure to attain 3B goals. Therefore, overweight or obese patients with type 2 diabetes should be encouraged to adopt preventive lifestyle interventions, including frequent exercise and restriction of smoking and drinking habits.
This analysis of a large, geographically diverse population of type 2 diabetes patients adds to our knowledge of the negative effects of overweight or obesity on control of cardiometabolic risk in patients with type 2 diabetes. The main study limitation was its cross-sectional design, which made it difficult to confirm a causal relationship between obesity and failure to achieve treatment goals. This needs to be further explored in subsequent follow-up analyses of the 3B Study. Also, because the WC data was incomplete in nearly half the patients, the difference in 3B control achieved by centrally obese and non-centrally obese patients might be subject to selection bias. In addition, we did not include data on adherence to antidiabetic medication in the analysis. Finally, because dietary data were not available in the 3B Study, the relationships between diet and obesity or diet and 3B control could not be evaluated.
Conclusions
Obesity was associated with poor control of blood glucose, blood pressure and blood lipids. The risk of cardiovascular complications thus remained increased in obese patients even though they were receiving more complex pharmacotherapy regimens than normal weight patients were. More attention and resources should be focused on encouraging and achieving weight loss and increased physical activity in patients with type 2 diabetes.
Supporting Information
Acknowledgments
The authors would like to thank all 3B study investigators (S1 Appendix) for their contribution to the successful completion of this study, and Dr. Jihu Li and Dr. Ruya Zhang of MSD China Holding Co., Ltd. for their assistance in preparing this manuscript.
Data Availability
All relevant data are available within the paper.
Funding Statement
This study was supported by an unrestricted research grant (#39103) from MSD China Holding Co., Ltd.(www.msdchina.com.cn) to LJ. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Yang W, Lu J, Weng J, Jia W, Ji L, Xiao J, China National Diabetes and Metabolic Disorders Study Group. et al. Prevalence of diabetes among men and women in China. N Engl J Med. 2010;362:1090–1101. 10.1056/NEJMoa0908292 [DOI] [PubMed] [Google Scholar]
- 2.Pan XR, Yang WY, Li GW, Liu J. Prevalence of diabetes and its risk factors in China, 1994. Diabetes Care. 1997;20:1664–1669 [DOI] [PubMed] [Google Scholar]
- 3.Reeder BA, Angel A, Ledoux M, Rabkin SW, Young TK, Sweet LE. Obesity and its relation to cardiovascular disease risk factors in Canadian adults. Canadian Heart Health Surveys Research Group. CMAJ. 1992;146:2009–2019. [PMC free article] [PubMed] [Google Scholar]
- 4.Said Q, Marx CM, Schwartz JS, Ben-Joseph R, Brixner DI. Impact of body mass index on the incidence of cardiometabolic risk factors in ambulatory care settings over 5 years or more. Value Health. 2010;13:265–272. 10.1111/j.1524-4733.2009.00649.x [DOI] [PubMed] [Google Scholar]
- 5.Félix-Redondo FJ, Grau M, Baena-Díez JM, Dégano IR, de León AC, Guembe MJ, et al. Prevalence of obesity and associated cardiovascular risk: the DARIOS study. BMC Public Health. 2013;13:542 10.1186/1471-2458-13-542 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Mokdad AH, Ford ES, Bowman BA, Dietz WH, Vinicor F, Bales VS,et al. Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001. JAMA. 2003;289:76–79. [DOI] [PubMed] [Google Scholar]
- 7.Carnethon MR, De Chavez PJ, Biggs ML, Lewis CE, Pankow JS, Bertoni AG, et al. Association of weight status with mortality in adults with incident diabetes. JAMA. 2012;308:581–590. 10.1001/jama.2012.9282 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Okafor CI, Ofoegbu EN. Control to goal of cardiometabolic risk factors among Nigerians living with type 2 diabetes mellitus. Niger J Clin Pract. 2012;15:15–18. 10.4103/1119-3077.94089 [DOI] [PubMed] [Google Scholar]
- 9.Hou X, Lu J, Weng J, Ji L, Shan Z, Liu J, et al. ; China National Diabetes and Metabolic Disorders Study Group. Impact of waist circumference and body mass index on risk of cardiometabolic disorder and cardiovascular disease in Chinese adults: a national diabetes and metabolic disorders survey. PLoS One. 2013;8:e57319 10.1371/journal.pone.0057319 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.American Diabetes Association. Standards of medical care in diabetes—2014. Diabetes Care. 2014;37:S14–80. 10.2337/dc14-S014 [DOI] [PubMed] [Google Scholar]
- 11.Authors/Task Force Members, Rydén L, Grant PJ, Anker SD, Berne C, Cosentino F, Danchin N,et al. ESC Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD: the Task Force on diabetes, pre-diabetes, and cardiovascular diseases of the European Society of Cardiology (ESC) and developed in collaboration with the European Association for the Study of Diabetes (EASD). Eur Heart J. 2013;34:3035–3087. 10.1093/eurheartj/eht108 [DOI] [PubMed] [Google Scholar]
- 12.Ji L, Hu D, Pan C, Weng J, Huo Y, Ma C, et al. Primacy of the 3B approach to control risk factors for cardiovascular disease in type 2 diabetes patients. Am J Med. 2013;126:925, e11–22. [DOI] [PubMed] [Google Scholar]
- 13.Zhou BF. Predictive values of body mass index and waist circumference for risk factors of certain related diseases in Chinese adults—study on optimal cut-off points of body mass index and waist circumference in Chinese adults. Biomed Environ Sci. 2002;15:83–96. [PubMed] [Google Scholar]
- 14.Zhou BF. Effect of body mass index on all-cause mortality and incidence of cardiovascular diseases—report for meta-analysis of prospective studies open optimal cut-off points of body mass index in Chinese adults. Biomed Environ Sci. 2002;15:245–252. [PubMed] [Google Scholar]
- 15.Wu Y. Overweight and obesity in China. BMJ. 2006;333:362–363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Chinese Diabetes Society. China Guideline for Type 2 Diabetes. Chin J Diabetes Mellitus. 2014;6:447–498 [Google Scholar]
- 17.American Diabetes Association. Cardiovascular Disease and Risk Management. Diabetes Care. 2015;38:S49–S57 10.2337/dc15-S011 [DOI] [PubMed] [Google Scholar]
- 18.Centers for Disease Control and Prevention (CDC). Prevalence of overweight and obesity among adults with diagnosed diabetes—United States, 1988–1994 and 1999–2002. MMWR Morb Mortal Wkly Rep. 2004;53:1066–1068. [PubMed] [Google Scholar]
- 19.Colosia AD, Palencia R, Khan S. Prevalence of hypertension and obesity in patients with type 2 diabetes mellitus in observational studies: a systematic literature review. Diabetes Metab Syndr Obes. 2013;6:327–338. 10.2147/DMSO.S51325 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Chehade JM, Gladysz M, Mooradian AD. Dyslipidemia in type 2 diabetes: prevalence, pathophysiology, and management. Drugs. 2013;73:327–339. 10.1007/s40265-013-0023-5 [DOI] [PubMed] [Google Scholar]
- 21.Iwahashi H, Okauchi Y, Ryo M, Noguchi M, Morita S, Kishida K, et al. Insulin-secretion capacity in normal glucose tolerance, impaired glucose tolerance, and diabetes in obese and non-obese Japanese patients. J Diabetes Invest. 2012;3:271–275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Daousi C, Casson IF, Gill GV, MacFarlane IA, Wilding JP, Pinkney JH. Prevalence of obesity in type 2 diabetes in secondary care: association with cardiovascular risk factors. Postgrad Med J. 2006;82:280–284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Look AHEAD Research Group, Wadden TA, Bantle JP, Blackburn GL, Bolin P, Brancati FL, Bray GA,et al. Cardiovascular effects of intensive lifestyle intervention in type 2 diabetes. N Engl J Med. 2013;369:145–154. 10.1056/NEJMoa1212914 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Ji L, Li H, Guo X, Li Y, Hu R, Zhu Z. Impact of baseline BMI on glycemic control and weight change with metformin monotherapy in Chinese type 2 diabetes patients: phase IV open-label trial. PLoS One. 2013;8:e57222 10.1371/journal.pone.0057222 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Pan C, Han P, Ji L, Ji Q, Lu J, Lin J, et al. Weight-neutral effect of once-daily insulin detemir in Chinese type 2 diabetes patients-subgroup analysis of the SOLVE study. J Diabetes. 2015; 7:222–230. 10.1111/1753-0407.12179 [DOI] [PubMed] [Google Scholar]
- 26.Jones DW, Miller ME, Wofford MR, Anderson DC Jr, Cameron ME, Willoughby DL, et al. The effect of weight loss intervention on antihypertensive medication requirements in the hypertension Optimal Treatment (HOT) study. Am J Hypertens. 1999;12:1175–1180. [DOI] [PubMed] [Google Scholar]
- 27.Fujioka K, Seaton TB, Rowe E, Jelinek CA, Raskin P, Lebovitz HE,et al. Weight loss with sibutramine improves glycaemic control and other metabolic parameters in obese patients with type 2 diabetes mellitus. Diabetes Obes Metab. 2000;2:175–187. [DOI] [PubMed] [Google Scholar]
- 28.Belletti DA, Zacker C, Wogen J. Effect of cardiometabolic risk factors on hypertension management: a cross-sectional study among 28 physician practices in the United States.Cardiovasc Diabetol. 2010;9:7 10.1186/1475-2840-9-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Qin L, Knol MJ, Corpeleijn E, Stolk RP. Does physical activity modify the risk of obesity for type 2 diabetes: a review of epidemiological data. Eur J Epidemiol. 2010;25:5–12. 10.1007/s10654-009-9395-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Ryan AS, Ge S, Blumenthal JB, Serra MC, Prior SJ, Goldberg AP. Aerobic exercise and weight loss reduce vascular markers of inflammation and improve insulin sensitivity in obese women. J Am Geriatr Soc. 2014;62:607–614. 10.1111/jgs.12749 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All relevant data are available within the paper.