Abstract
Background
The associations between physical activity and metabolic syndrome (MetS) have been mainly found in cross-sectional studies. The aim of this longitudinal study was to examine the relationship between meeting step-based guidelines and changes in the risk of metabolic syndrome.
Methods
This study included data from older women (baseline age 62.9 ± 4.3 years) from a 7-year longitudinal study in Central Europe. At baseline and follow-up, physical activity was measured by an accelerometer, and the risk for MetS was assessed according to the NCEP-ATP III criteria. In 59 women, multivariate repeated measures ANOVA was used to compare differences in changes in the risk of MetS in groups based on meeting step-based guidelines (10,000 steps/day and 9000 steps/day for women aged <65 and ≥ 65 years, respectively).
Results
Over 7 years, steps/day increased from 10,944 ± 3560 to 11,652 ± 4865, and the risk of MetS decreased from 41 to 12% in our sample. Women who longitudinally met step-based guidelines had a significantly higher mean concentration of high-density cholesterol (HDL-C) (64.5 and 80.3 mg/dL at baseline and follow-up, respectively) and a lower concentration of triglycerides (TGs) (158.3 and 123.8 mg/dL at baseline and follow-up, respectively) at follow-up compared to baseline. Moreover, women who increased their daily steps over 7 years to the recommended steps/day value significantly decreased the concentration of TGs (158.3 mg/dL and 123.8 mg/dL at baseline and follow-up, respectively).
Conclusions
Our study might suggest that the long-term meeting of step-based guidelines or an increase in daily steps/day to achieve the recommended value could be related to a lower risk of MetS, specifically in concentrations of HDL-C and TG. These findings may help in designing interventions aiming to decrease the risk of MetS in older women.
Keywords: Health, Daily physical activity, Accelerometer, MetS components, Number of steps
Background
The concomitance of high blood pressure, hyperglycaemia, central obesity, and elevated cholesterol or triglyceride levels, known as metabolic syndrome (MetS), is indicated as one of the major socioeconomic problems faced by the contemporary world [1]. Research shows that MetS increases the risk of type 2 diabetes mellitus and cardiovascular diseases, and its components are among the main causes of death worldwide [2]. An early and accurate diagnosis of MetS enabling the application of effective therapies can therefore be very instrumental in protecting the health and well-being of populations [1]. This is particularly the case in older adults because the risk for MetS increases with age [3].
There is a growing body of evidence that the risk of developing MetS can be reduced by physical activity [4]. While most authors point to moderate-to-vigorous exercise as being much more effective [5] than light-intensity exercise [4], there is general consent that all attempts to quit a sedentary lifestyle can help prevent the development of MetS [6].
Older people, who are the most sedentary within the population [7] and develop MetS the most often [3, 8], are recommended to choose moderate-to-higher intensity exercise such as walking. As a low-impact and affordable form of exercise requiring neither special skills nor equipment [9], walking is very well suited to the needs and physical capabilities of older people. It also has advantages over other sports and recreational activities in that can be easily included in one’s daily activities and practised at very old ages [9]. It is also of importance that the increasing availability of step-counting technology makes it possible for people to monitor and regulate their daily physical activity [10].
The authors of a recent systematic review found an inverse relationship between the number of steps taken daily and the presence of MetS [4]. In the case of middle-aged and older adults, it is recommended that they take 10,000 steps per day to prevent the development of MetS [11–14].
Strong associations between the daily number of steps and the risk of MetS development are mostly reported by the authors of cross-sectional studies [15]. Relatively few longitudinal studies have thus far been undertaken to determine relationships between physical activity in older adults and age and their risk of MetS [16].
Given the higher prevalence of MetS in women than men [3] and the lack of longitudinal studies investigating changes in MetS related to physical activity, the aim of this study was to examine the relationship between long-term meetings of step-based guidelines (10,000 steps/day and 9000 steps/day for women aged <65 and ≥ 65 years, respectively) and changes in the risk of MetS in older women. Considering that the risk of MetS can be reduced by physical activity [4], we hypothesized that older women longitudinally meeting the step-based guidelines would have a lower risk of MetS.
Methods
Design and participants
We analysed the data from a longitudinal study in older women from Central European countries, which has been described elsewhere [17]. One hundred and six physically active women aged 60+ participating in a programme run at the University of Third Age (U3A) were invited to participate in this study. Of those, 51 failed to meet the study inclusion criteria, which required the participants to be able to walk without a prosthetic aid, not use medications for metabolic disorders, and not smoke cigarettes. Therefore, 89 women were assessed during the baseline stage. Over the 7-year period, 2 participants died, 7 had no contact, 5 were ineligible, and 12 refused to participate in the study again.
All the women were informed that their participation was voluntary and that they could withdraw from the study at any time. They provided their written consent for both baseline and follow-up stages.
This study was approved by the Ethics Commission at The Jerzy Kukuczka Academy of Physical Education (reference number. 3/2009). Moreover, an overarching longitudinal study in Central European countries was approved by the Institutional Research Ethics Committee, Faculty of Physical Culture, Palacký University Olomouc (reference number 20/2017).
Biochemical and anthropometric assessments
Between 8:00 and 10:00 a.m., fasting blood samples were taken from participants, and their systolic/diastolic blood pressure (SDP and DBP, respectively) was measured using a standard mercury sphygmomanometer. The results of two measurements taken at an interval of 15 min were averaged for analysis. The serum concentrations of glucose, high-density lipoprotein cholesterol (HDL-C), and serum triglycerides (TG) were determined using enzymatic assays and commercially available diagnostic kits (Randox UK, cat. no. GL 2623, CH 200, CH 203, TR 1697). Serum was separated in the usual manner and analysed immediately or kept frozen at − 80 °C until analysis.
Waist circumference (WC) was determined to the nearest 0.5 cm using anthropometric tape midway between the lowest rib and the iliac crest in a standing position. The percentages of body fat (PBF) and visceral fat area (VFA) at the umbilical level were determined using an InBody 720 analyser [18, 19] according to the manufacturer’s instructions (Biospace Co., Ltd., Seoul, Korea).
The presence of MetS was determined in line with the NCEP/ATP III revised guidelines [20]. According to the guidelines, MetS occurs when three or more of the following criteria are met: (1) WC ≥88 cm; (2) TG ≥150 mg/dl; 3) HDL-C < 50 mg/dL; 4) systolic blood pressure (SBP) ≥130 mmHg and diastolic blood pressure (DBP) ≥85 mmHg; and 5) fasting glucose level ≥ 100 mg/dl.
Physical activity assessment
At baseline and follow-up, the participants’ physical activity (PA) was measured using an accelerometer (ActiGraph GT1M, Manufacturing Technology Inc., FL, USA). The accelerometers were worn by the participants in the small pockets of the elastic belts positioned near the right iliac crest for at least 12 h each day over a period of 8 days and were only removed for water exercises and before bedtime. The first day’s readings were excluded from analysis to ensure that the potential reactivity of participants did not compromise the reliability of measurements [21]. All the participants were instructed to record the duration and type of each physical activity they performed during the day (e.g., walking for 10 min).
The time sampling interval of the accelerometers was set at 1 min, an epoch commonly used to measure free-living physical activity (PA) and in epidemiological research [21], and the step mode was activated. The accelerometer readings were processed in ActiLife v6.13.1 (Pensacola, FL, USA).
Other assessments
Several self-rated data were obtained from the participants. Smoking status and education level were obtained at both time points. At follow-up, the participants were retrospectively asked about their dietary habits over the 7 years and possible treatment for metabolic disorders.
Data and statistical analysis
The statistical analysis of the data was performed in STATISTICA 12.5 (StatSoft, USA). The descriptive statistics represent means and their 95% confidence intervals. Moreover, the numbers and percentages of women meeting the diagnostic criteria for each MetS component and step-based guidelines were calculated for baseline and follow-up. The number of steps/day was selected as a commonly used indicator of physical activity level in adults and older adults [22–25].
To divide women aged < 65 and ≥ 65 years into physically highly active (meeting step-based guidelines) and physically low active (not meeting step-based guidelines), threshold values of 10,000 and 9000 steps per day, respectively, were used. The first number was adopted from Bassett et al. [15], Freak-Poli et al. [26], Harris et al. [27], and Tudor-Locke et al. [28], who recommend that adults take at least 10,000 steps per day to stay healthy. For women aged 65+, it was lowered to account for the likely effect of their age on their activity.
Based on meeting daily step-based guidelines at baseline and follow-up, women were divided into four physical activity groups. Women in the low-low (LL) group were below the recommended step-based thresholds at both baseline and follow-up. Women in the high-low (HL) group reached their step-based thresholds only at baseline and those in the low-high (LH) group only at follow-up. The high-high (HH) group included women who met step-based guidelines at both time points.
Differences between participants’ anthropometric parameters, MetS components, and physical activity levels measured in 2009 and 2016, as well as between-group differences in the number of steps, were assessed for statistical significance using a paired t-test. The longitudinal changes in MetS components (the effect of time, TE), the between-group differences in MetS components (the effect of physical activity, PAE), and the associations between the groups’ physical activity and changes in MetS components (the interaction effect, INT) were assessed by multivariate repeated-measures ANOVA (MANOVA). The effect size was determined by calculating eta squared (η2) as per the following formula: η2 = SS effect/SS total, where SS effect is the sum of squares for a given effect and SS total is the total of squares for all effects, interactions, and errors [29]. The 95% confidence intervals calculated for individual MetS components were also analysed [30, 31].
Results
Out of 106 older women, the analytical sample consisted of 59 women with a mean baseline age of 62.9 ± 4.3 years and baseline BMI of 26.8 ± 4.2 kg/m2 at baseline, having tertiary (35.6%), secondary (59.2%), and primary (15.2%) education. The women reported no smoking, no change in their dietary habits and no treatment for metabolic disorders for 7 years. Other sample characteristics for baseline and follow-up are shown in Table 1.
Table 1.
Characteristic | Baseline | Follow-up | Difference | ||
---|---|---|---|---|---|
M | 95% CI | M | 95% CI | % | |
Anthropometrics | |||||
Height (m) | 158.2 | (156.9, 159.6) | 157.3 | (155.9, 158.7) | 0.6 |
Weight (kg) | 67.1 | (64.4, 69.8) | 68.0 | (65.2, 70.7) | −1.2 |
BMI (kg/m2) | 26.8 | (25.8, 27.9) | 27.7 | (26.5, 28.8) | 3.2* |
VFA (cm2) | 133.3 | (125.2, 141,4) | 131.0 | (121.6, 140.4) | −1.7 |
PBF (%) | 36.8 | (34.9, 38.6) | 39.1 | (37.2, 40.9) | 6.3* |
Metabolic syndrome | |||||
WC (cm) | 84.1 | (81.2, 87.1) | 85.1 | (82.3, 87.9) | 1.2 |
Fasting glucose (mg/dL) | 90.3 | (86.9, 93.6) | 98.8 | (95.1, 102.5) | 9.4* |
HDL-C (mg/dL) | 64.4 | (60.0, 68.8) | 76.5 | (71.6, 81.3) | 18.8* |
TG (mg/dL) | 127.5 | (115.0, 140.0) | 106.3 | (94.9, 117.7) | −16.6* |
SBP (mmHg) | 129.8 | (125.7, 133.9) | 135.4 | (130.3, 140.5) | 4.3 |
DBP (mmHg) | 77.0 | (74.5, 79.6) | 79.9 | (77.1, 82.7) | 3.8 |
No. of MetS criteria | 2.2 | (1.9, 2.6) | 1.4 | (1.2, 1.7) | −35.6* |
Risk of MetS (N, %) | 24 | 40.1 | 7 | 11.8 | −30.8* |
Physical activity | |||||
Steps/day | 10.944 | (10.006, 11.882) | 11,652 | (10.384, 12.920) | 6.5 |
Steps/day aged < 65 years | 11.596 | (10.379, 12.814) | 12.847 | (11.280, 14.414) | 10.8 |
Steps/day aged ≥65 years | 9.673 | (8.285, 11.060) | 9.322 | (7.399, 11.244) | −3.3 |
M Mean, 95% CI Confidence interval, BMI Body mass index, VFA Visceral fat area, PBF Percent body fat, WC Waist circumference, HDL-C High-density lipoprotein cholesterol, TG Triglycerides, SBP Systolic blood pressure, DBP Diastolic blood pressure, MetS Metabolic syndrome
* – statistically significant at p < .001
Over 7 years, BMI and PBF significantly increased by 3.2 and 6.3%, respectively, but the risk of MetS decreased from 39 to 12%, and the mean number of criteria for MetS fell by 35.6%. Decreases were also noted in the concentrations of HDL-C and TG, which are MetS risk factors.
Figure 1 and Table 2 show the range of participants meeting different MetS criteria (0–5). Over 7 years, the number of women who met 3 or more criteria for MetS decreased from 24 to 7. At follow-up, the numbers of participants with elevated TG and BP concentrations and WC ≥ 88 cm decreased by 50, 32.5, and 36.1%, respectively, but the number of women with raised fasting glucose (< 100 mg/dL) increased by 23%. The number of participants with normal HDL-C increased by 58.6%.
Table 2.
MetS component | No. of participants meeting the criterion | No. of participants not meeting the criterion | ||
---|---|---|---|---|
Baseline | Follow-up | Baseline | Follow-up | |
n (%) | n (%) | n (%) | n (%) | |
HDL-C | 25 (42.4) | 1 (1.7) | 34 (57.6) | 58 (98.3) |
TG | 16 (27.0) | 8 (13.6) | 43 (73.0) | 51 (86.4) |
Fasting glucose | 15 (25.5) | 23 (39.0) | 44 (74.5) | 36 (61.0) |
BP | 40 (68.0) | 27 (46.0) | 19 (32.0) | 32 (54.0) |
WC | 36 (61.0) | 23 (39.0) | 23 (39.0) | 36 (61.0) |
HDL-C High-density cholesterol, TG Triglycerides, BP Blood pressure, WC Waist circumference
Long-term differences in steps/day were not significant. However, it is clear from Table 1 that women increased their mean steps/day by 6.5% (10,944 and 11,652 steps/day at baseline and follow-up, respectively). This was mainly due to an increase in daily steps in women aged < 65 (11,596 and 12,847 steps/day at baseline and follow-up, respectively).
Table 3 shows 7-year changes in steps/day in different physical activity groups. Groups LH and HH significantly increased daily steps (p = 0.002 and p = 0.04, respectively), while the HL group significantly decreased steps/day (p = 0.012). No change was found for the LL group.
Table 3.
Groupa | N | Baseline | Follow-up | ||||
---|---|---|---|---|---|---|---|
Age | Steps/day | Age | Steps/day | ||||
M | M | 95% CI | M | M | 95% CI | ||
LL | 12 | 66.0 | 7189 | (6146, 8231) | 73.0 | 6258 | (5068, 7447) |
HL | 9 | 64.7 | 11,182 | (9094, 13,269) | 71.7 | 7441* | (5797, 9084) |
LH | 10 | 60.8 | 8005 | (7463, 8546) | 67.8 | 13247* | (10,538, 15,957) |
HH | 28 | 61.7 | 13,527 | (12,434, 14,621) | 68.7 | 14747* | (13,319, 16,175) |
M Mean, 95% CI Confidence interval
* – statistically significant at p < 0.05
a LL Low-low group (women not meeting step-based guidelines nor in baseline neither in follow-up), HL High-low group (women meeting step-based guidelines at baseline but not in follow-up), LH Low-high group (women meeting step-based guidelines at follow-up but not in baseline), HH High-high group (women meeting step-based guidelines at both time points)
Changes in physical activity and the risk for MetS
According to MANOVA (Fig. 2a-f), significant changes between baseline and follow-up were found for the concentrations of HDL-C (F = 15.789, p < 0.001), TG (F = 17.182, p < 0.001) and fasting glucose (F = 19.309, p < 0.001). The effect of time (TE) was not significant for SBP, DBP, or WC. In follow-up, the HH group and the LH group had significantly higher concentrations of HDL-C than at baseline (64.5 mg/dL [CI: 58.8, 70.2] vs. 80.3 [CI: 73.2, 87.3] and 66.9 [CI: 55.2., 78.6] vs. 79.2 [CI: 73.2, 87.3], respectively). Moreover, the LH group had a significantly decreased concentration of TG (158.3 mg/dL [CI: 105.4, 211.2] vs. 123.8 mg/dL [CI: 82.3, 165.4]). TG decreases in the other three groups were not significant.
All groups had higher levels of fasting glucose in follow-up, but significant changes were noted only in the HH group (87.6 mg/dL [CI: 81.9, 90.3] vs. 95.8 mg/dL [CI: 99.9, 100.8]) and the LL group (94.3 mg/dL [CI: 86.0, 102.7] vs. 107.3 mg/dL [CI: 94.3, 120.3]). The fasting glucose level in the HH group was < 100 mg/dL in both 2009 and 2016.
WC was the only one of the five MetS components that was associated with the levels of participants’ physical activity (F = 5.392, p = 0.003). At baseline, the HH, LH, and HL groups had smaller mean WCs than the LL group. After 7 years, it was still smaller in the groups that had maintained or increased physical activity (HH and LH), but in the HL group, it increased and was similar to the LL group’s WC.
The interaction effect of time and physical activity was not significant in any of the MetS criteria.
Discussion
Our longitudinal study in older women suggests a decreasing risk of MetS in longitudinally active older women. Although the effect of group and time was not significant in any of the MetS criteria, women with recommended values of steps/day at baseline and follow-up and women who increased their daily steps over 7 years and met the guidelines in follow-up improved their values in several MetS criteria, mainly in concentrations of HDL-C and TG. Conversely, older women longitudinally not meeting the step-based guidelines had risk values of WC at baseline and follow-up and risk values of fasting glucose at baseline.
Looking at the mean values of steps/day at baseline and follow-up and a 6.5% increase during the 7-year period, our sample consisted of very active women in comparison with the average values of healthy older adults based on normative data [32] and did not support the expected age-related decrease in daily physical activity [33–35]. On the other hand, BMI and PBF significantly increased over 7 years, which is in concordance with other longitudinal studies [36, 37].
It should be mentioned that overweight and obesity may lead to metabolic syndrome after menopause [38–40], especially in older women [41]. In our sample, the risk of MetS decreased over time, although the average values of BMI and PBF were in the overweight (25–29.9 kg/m2) and obesity (> 35%) categories at baseline and follow-up. However, abdominal obesity indicators, VFA and WC, which did not change, could be stronger predictors of MetS in older women [14, 42].
In this study, we found improvement in HDL-C and TG in the whole sample, but with the largest change in women in the HH group (longitudinally meeting steps/day guidelines) and in women in the LH group (meeting the guidelines in follow-up). On the other hand, deterioration was found in fasting glucose in the sample, but only women in the LL group (not longitudinally meeting steps/day guidelines) or HL group (not meeting steps guidelines at follow-up) exceeded the risk cut-off point ≥100 mg/dl. WC was the highest in the women longitudinally not meeting the step/day recommendation and in women who decreased their steps/day over 7 years. These findings might confirm previous studies suggesting that the risk values of different MetS components can be reduced by exercise and sufficient physical activity [43–46]. Our findings are in line with the USA study [13], suggesting that adults who took more steps/day tended to have lower WC, higher HDL-C, and lower levels of TG. Additionally, a recent review [4] reported a negative association with MetS in all studies assessing step counts.
The strengths of this study are its longitudinal design with a long follow-up duration and objective assessments of physical activity and MetS criteria. The limitations of the study are mainly the relatively small number of participants impeding the generalization of its results and reducing the power of statistical testing. Moreover, the results of the study were not adjusted for dietary information, although the impact of specific food or products on the risk of MetS was suggested in previous studies [47–49]. Additionally, genetic information, family history or comorbidities that could be related to the risk of MetS were not considered in this study. Another limitation lies in the treatment of physical activity. Steps/day were already used in some previous studies, enabling valuable comparison [4, 13]. However, they did not provide information on the intensity and type of physical activity that might influence the strengths of associations between physical activity and risk of MetS [4].
Conclusion
Our longitudinal study in a cohort of active older women might suggest that the long-term meeting of step-based guidelines or longitudinal increases in daily steps/day to achieve the recommended value could be related to a lower risk of MetS, specifically in concentrations of HDL-C and TG. These findings may help in designing interventions aiming to decrease the risk of MetS in older women.
Acknowledgements
The authors wish to thank the study participants for their commitment and cooperation. The financial support offered by the Jerzy Kukuczka Academy of Physical Education and the Czech Science Foundation is also gratefully acknowledged.
Abbreviations
- MetS
Metabolic syndrome
- HDL-C
High-density cholesterol
- TG
Triglycerides
- VFA
Visceral fat accumulation
- BMI
Body mass index
- PBF
Percent body fat
- BP
Blood pressure
- DBP
Diastolic blood pressure
- SDP
Systolic blood pressure
- WC
Waist circumference
- PA
Physical activity
- 95% CI
Confidence interval
- TE
The effect of time
- PAE
The effect of physical activity
- INT
The interaction effect
- TE
The effect of time
- LL
Low physical activity at baseline (2009) and follow-up (2016)
- HL
High physical activity at baseline (2009) and low at follow-up (2016)
- LH
Low physical activity at baseline (2009) and high at follow-up (2016)
- HH
High physical activity at baseline (2009) and follow-up (2016)
Authors’ contributions
IZG – study design and supervision, data collection and analysis, manuscript writing; JP – study design and manuscript writing; DG – study design and proofreading of the manuscript; MP – data collection and manuscript proofreading; ANS – data collection and manuscript proofreading; AK – data analysis and manuscript proofreading; AG – data collection and manuscript proofreading; ESK – biochemical blood tests, analysis of their results, and manuscript proofreading. The final version of the manuscript and its publication were unanimously approved.
Funding
The study was jointly funded by the Czech Science Foundation (research grant No. 18-16423S) and the Jerzy Kukuczka Academy of Physical Education (under statutory funding). The funding sources had no role in the design of the study and did not have any role in collection, analysis, and interpretation of data or in writing the manuscript.
Availability of data and materials
The dataset analyzed during the current study is available in the Figshare repository, https://figshare.com/articles/dataset/Dataset/13234544.
Ethics approval and consent to participate
This study was approved by the Ethics Commission at The Jerzy Kukuczka Academy of Physical Education (reference number. 3/2009). Moreover, an overarching longitudinal study in Central European countries was approved by the Institutional Research Ethics Committee, Faculty of Physical Culture, Palacký University Olomouc (reference number 20/2017). and was performed in accordance with the Declaration of Helsinki. All participants agreed in writing to participate in the study. The consent forms are in possession of the authors and can be made available upon request.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.O’Neill S, O’Driscoll L. Metabolic syndrome: a closer look at the growing epidemic and its associated pathologies. Obes Rev. 2015;16:1–12. doi: 10.1111/obr.12229. [DOI] [PubMed] [Google Scholar]
- 2.Wilson PWF, D’Agostino RB, Parise H, Sullivan L, Meigs JB. Metabolic syndrome as a precursor of cardiovascular disease and type 2 diabetes mellitus. Circulation. 2005;112:3066–3072. doi: 10.1161/CIRCULATIONAHA.105.539528. [DOI] [PubMed] [Google Scholar]
- 3.Aguilar M, Bhuket T, Torres S, Liu B, Wong RJ. Prevalence of the metabolic syndrome in the United States, 2003-2012. JAMA. 2015;313:1973–1974. doi: 10.1001/jama.2015.4260. [DOI] [PubMed] [Google Scholar]
- 4.Amirfaiz S, Shahril MR. Objectively measured physical activity, sedentary behavior, and metabolic syndrome in adults: systematic review of observational evidence. Metab Syndr Relat Disord. 2019;17(1):1–21. doi: 10.1089/met.2018.0032. [DOI] [PubMed] [Google Scholar]
- 5.Rennie K, McCarthy N, Yazdgerdi S, Marmot M, Brunner E. Association of the metabolic syndrome with both vigorous and moderate physical activity. Int J Epidemiol. 2003;32:600–606. doi: 10.1093/ije/dyg179. [DOI] [PubMed] [Google Scholar]
- 6.Edwardson CL, Gorely T, Davies MJ, Gray LJ, Khunti K, Wilmot EG, et al. Association of sedentary behaviour with metabolic syndrome: a meta-analysis. PLoS One. 2012;7:e34916. doi: 10.1371/journal.pone.0034916. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Harvey JA, Chastin SFM, Skelton DA. How sedentary are older people? A systematic review of the amount of sedentary behavior. J Aging Phys Act. 2015;23:471–487. doi: 10.1123/japa.2014-0164. [DOI] [PubMed] [Google Scholar]
- 8.Chuang T-J, Huang C-L, Lee C-H, Hsieh C-H, Hung Y-J, Hung C-F, et al. The differences of metabolic syndrome in elderly subgroups: a special focus on young-old, old-old and oldest old. Arch Gerontol Geriatr. 2016;65:92–97. doi: 10.1016/j.archger.2016.03.008. [DOI] [PubMed] [Google Scholar]
- 9.Ogilvie D, Foster CE, Rothnie H, Cavill N, Hamilton V, Fitzsimons CF, et al. Interventions to promote walking: systematic review. BMJ. 2007;334:1204. doi: 10.1136/bmj.39198.722720.BE. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Tudor-Locke C, Han H, Aguiar EJ, Barreira TV, Schuna JM, Jr, Kang M, et al. How fast is fast enough? Walking cadence (steps/min) as a practical estimate of intensity in adults: a narrative review. Br J Sports Med. 2018;52:776–788. doi: 10.1136/bjsports-2017-097628. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Cocate PG, de Oliveira A, Hermsdorff HHM, Rita de Cássia GA, Amorim PRS, Longo GZ, et al. Benefits and relationship of steps walked per day to cardiometabolic risk factor in Brazilian middle-aged men. J Sci Med Sport. 2014;17:283–287. doi: 10.1016/j.jsams.2013.04.017. [DOI] [PubMed] [Google Scholar]
- 12.Schmidt MD, Cleland VJ, Shaw K, Dwyer T, Venn AJ. Cardiometabolic risk in younger and older adults across an index of ambulatory activity. Am J Prev Med. 2009;37:278–284. doi: 10.1016/j.amepre.2009.05.020. [DOI] [PubMed] [Google Scholar]
- 13.Sisson SB, Camhi SM, Church TS, Tudor-Locke C, Johnson WD, Katzmarzyk PT. Accelerometer-determined steps/day and metabolic syndrome. Am J Prev Med. 2010;38:575–582. doi: 10.1016/j.amepre.2010.02.015. [DOI] [PubMed] [Google Scholar]
- 14.Zając-Gawlak I, Kłapcińska B, Kroemeke A, Pośpiech D, Pelclová J, Přidalová M. Associations of visceral fat area and physical activity levels with the risk of metabolic syndrome in postmenopausal women. Biogerontology. 2017;18:357–366. doi: 10.1007/s10522-017-9693-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Bassett DR, Jr, Toth LP, LaMunion SR, Crouter SE. Step counting: a review of measurement considerations and health-related applications. Sports Med (Auckland, NZ) 2017;47:1303–1315. doi: 10.1007/s40279-016-0663-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Chen L-J, Lai Y-J, Sun W-J, Fox KR, Chu D, Ku P-W. Associations of exercise, sedentary time and insomnia with metabolic syndrome in Taiwanese older adults: a 1-year follow-up study. Endocr Res. 2015;40:220–226. doi: 10.3109/07435800.2015.1020547. [DOI] [PubMed] [Google Scholar]
- 17.Cuberek R, Pelclová J, Gába A, Pechová J, Svozilová Z, Přidalová M, et al. Adiposity and changes in movement-related behaviors in older adult women in the context of the built environment: a protocol for a prospective cohort study. BMC Public Health. 2019;19:1–7. doi: 10.1186/s12889-019-7905-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Ogawa H, Fujitani K, Tsujinaka T, Imanishi K, Shirakata H, Kantani A, et al. InBody 720 as a new method of evaluating visceral obesity. Hepatogastroenterology. 2011;58:42–44. [PubMed] [Google Scholar]
- 19.Park KS, Lee D-H, Lee J, Kim YJ, Jung KY, Kim KM, et al. Comparison between two methods of bioelectrical impedance analyses for accuracy in measuring abdominal visceral fat area. J Diabetes Complicat. 2016;30:343–349. doi: 10.1016/j.jdiacomp.2015.10.014. [DOI] [PubMed] [Google Scholar]
- 20.Grundy SM, Brewer HB, Cleeman JI, Smith SC, Lenfant C. Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition. Circulation. 2004;109:433–438. doi: 10.1161/01.CIR.0000111245.75752.C6. [DOI] [PubMed] [Google Scholar]
- 21.Esliger DW, Copeland JL, Barnes JD, Tremblay MS. Standardizing and optimizing the use of accelerometer data for free-living physical activity monitoring. J Phys Act Health. 2005;2:366–383. doi: 10.1123/jpah.2.3.366. [DOI] [Google Scholar]
- 22.Tudor-Locke C, Bassett DR. How many steps/day are enough? Preliminary pedometer indices for public health. Sports Med. 2004;34:1–8. doi: 10.2165/00007256-200434010-00001. [DOI] [PubMed] [Google Scholar]
- 23.Choi BCK, Pak AWP, Choi JCL, Choi ECL. Daily step goal of 10,000 steps: a literature review. Clin Invest Med. 2007;30:E146–E151. doi: 10.25011/cim.v30i3.1083. [DOI] [PubMed] [Google Scholar]
- 24.Tudor-Locke C, Hatano Y, Pangrazi RP, Kang M. Revisiting “how many steps are enough?”. Med Sci Sports Exerc. 2008;40(7 Suppl):S537–S543. doi: 10.1249/MSS.0b013e31817c7133. [DOI] [PubMed] [Google Scholar]
- 25.Aoyagi Y, Shephard RJ. Habitual physical activity and health in the elderly: the Nakanojo study. Geriatr Gerontol Int. 2010;10(Suppl 1):S236–S243. doi: 10.1111/j.1447-0594.2010.00589.x. [DOI] [PubMed] [Google Scholar]
- 26.Freak-Poli RLA, Cumpston M, Peeters A, Clemes SA. Workplace pedometer interventions for increasing physical activity. Cochrane Database Syst Rev. 2013:CD009209. 10.1002/14651858.CD009209.pub2. [DOI] [PubMed]
- 27.Harris T, Kerry SM, Limb ES, Furness C, Wahlich C, Victor CR, et al. Physical activity levels in adults and older adults 3-4 years after pedometer-based walking interventions: long-term follow-up of participants from two randomised controlled trials in UK primary care. PLoS Med. 2018;15:e1002526. doi: 10.1371/journal.pmed.1002526. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Tudor-Locke C, Craig CL, Brown WJ, Clemes SA, De Cocker K, Giles-Corti B, et al. How many steps/day are enough? For adults. Int J Behav Nutr Phys Act. 2011;8:79. doi: 10.1186/1479-5868-8-79. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Vacha-Haase T, Thompson B. How to estimate and interpret various effect sizes. J Couns Psychol. 2004;51:473–481. doi: 10.1037/0022-0167.51.4.473. [DOI] [Google Scholar]
- 30.Hopkins WG, Batterham AM, Marshall SW, Hanin J. Progressive statistics. Sport Sci. 2009;41(1):3–13. doi: 10.1249/MSS.0b013e31818cb278. [DOI] [PubMed] [Google Scholar]
- 31.Shieh G. Confidence intervals and sample size calculations for the weighted eta-squared effect sizes in one-way heteroscedastic ANOVA. Behav Res Methods. 2013;45:25–37. doi: 10.3758/s13428-012-0228-7. [DOI] [PubMed] [Google Scholar]
- 32.Tudor-Locke C, Craig CL, Aoyagi Y, Bell RC, Croteau KA, De Bourdeaudhuij I, et al. How many steps/day are enough? For older adults and special populations. Int J Behav Nutr Phys Act. 2011;8:80. doi: 10.1186/1479-5868-8-80. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Doherty A, Jackson D, Hammerla N, Plötz T, Olivier P, Granat MH, et al. Large scale population assessment of physical activity using wrist worn accelerometers: the UK biobank study. PLoS One. 2017;12(2):e0169649. doi: 10.1371/journal.pone.0169649. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Berkemeyer K, Wijndaele K, White T, Cooper AJM, Luben R, Westgate K, et al. The descriptive epidemiology of accelerometer-measured physical activity in older adults. Int J Behav Nutr Phys Act. 2016;13(1):2. doi: 10.1186/s12966-015-0316-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Troiano RP, Berrigan D, Dodd KW, Mâsse LC, Tilert T, McDowell M. Physical activity in the United States measured by accelerometer. Med Sci Sports Exerc. 2008;40:181–188. doi: 10.1249/mss.0b013e31815a51b3. [DOI] [PubMed] [Google Scholar]
- 36.Hughes VA, Frontera WR, Roubenoff R, Evans WJ, Singh MAF. Longitudinal changes in body composition in older men and women: role of body weight change and physical activity. Am J Clin Nutr. 2002;76(2):473–481. doi: 10.1093/ajcn/76.2.473. [DOI] [PubMed] [Google Scholar]
- 37.Raguso CA, Kyle U, Kossovsky MP, Roynette C, Paoloni-Giacobino A, Hans D, et al. A 3-year longitudinal study on body composition changes in the elderly: role of physical exercise. Clin Nutr. 2006;25(4):573–580. doi: 10.1016/j.clnu.2005.10.013. [DOI] [PubMed] [Google Scholar]
- 38.Carr MC. The emergence of the metabolic syndrome with menopause. J Clin Endocrinol Metab. 2003;88:2404–2411. doi: 10.1210/jc.2003-030242. [DOI] [PubMed] [Google Scholar]
- 39.Jouyandeh Z, Nayebzadeh F, Qorbani M, Asadi M. Metabolic syndrome and menopause. J Diabetes Metab Disord. 2013;12:1. doi: 10.1186/2251-6581-12-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Polotsky HN, Polotsky AJ. Metabolic implications of menopause. Semin Reprod Med. 2010;28:426–434. doi: 10.1055/s-0030-1262902. [DOI] [PubMed] [Google Scholar]
- 41.Pucci G, Alcidi R, Tap L, Battista F, Mattace-Raso F, Schillaci G. Sex-and gender-related prevalence, cardiovascular risk and therapeutic approach in metabolic syndrome: a review of the literature. Pharmacol Res. 2017;120:34–42. doi: 10.1016/j.phrs.2017.03.008. [DOI] [PubMed] [Google Scholar]
- 42.Kang SH, Cho KH, Park JW, Do JY. Comparison of waist to height ratio and body indices for prediction of metabolic disturbances in the Korean population: the Korean National Health and nutrition examination survey 2008–2011. BMC Endocr Disord. 2015;15:79. doi: 10.1186/s12902-015-0075-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Gordon B, Chen S, Durstine JL. The effects of exercise training on the traditional lipid profile and beyond. Curr Sports Med Rep. 2014;13:253–259. doi: 10.1249/JSR.0000000000000073. [DOI] [PubMed] [Google Scholar]
- 44.Marliss EB, Vranic M. Intense exercise has unique effects on both insulin release and its roles in glucoregulation: implications for diabetes. Diabetes. 2002;51(Suppl 1):S271–S283. doi: 10.2337/diabetes.51.2007.S271. [DOI] [PubMed] [Google Scholar]
- 45.Durstine JL, Grandjean PW, Davis PG, Ferguson MA, Alderson NL, DuBose KD. Blood lipid and lipoprotein adaptations to exercise: a quantitative analysis. Sports Med (Auckland, NZ) 2001;31:1033–1062. doi: 10.2165/00007256-200131150-00002. [DOI] [PubMed] [Google Scholar]
- 46.Durstine JL, Grandjean PW, Cox CA, Thompson PD. Lipids, lipoproteins, and exercise. J Cardpulm Rehabil. 2002;22:385–398. doi: 10.1097/00008483-200211000-00002. [DOI] [PubMed] [Google Scholar]
- 47.Kastorini CM, Milionis HJ, Esposito K, et al. The effect of mediterranean diet on metabolic syndrome and its components: a meta-analysis of 50 studies and 534,906 individuals. J Am Coll Cardiol. 2011;57:1299–1313. doi: 10.1016/j.jacc.2010.09.073. [DOI] [PubMed] [Google Scholar]
- 48.Sayon-Orea C, Martínez-González MA, Ruiz-Canela M, Bes-Rastrollo M. Associations between yogurt consumption and weight gain and risk of obesity and metabolic syndrome: a systematic review. Adv Nutr. 2017;8(1):146S–154S. doi: 10.3945/an.115.011536. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Shin JY, Kim JY, Kang HT, Han KH, Shim JY. Effect of fruits and vegetables on metabolic syndrome: a systematic review and meta-analysis of randomized controlled trials. Int J Food Sci Nutr. 2015;66(4):416–425. doi: 10.3109/09637486.2015.1025716. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The dataset analyzed during the current study is available in the Figshare repository, https://figshare.com/articles/dataset/Dataset/13234544.