Better Option for Improving Metabolic Syndrome: Consideration of the Amount and Duration of Resistance Exercise or Physical Activity

Article information

Exerc Sci. 2023;32(2):222-230
Publication date (electronic) : 2023 May 31
doi : https://doi.org/10.15857/ksep.2023.00241
Sports Medicine Lab., Department of Physical Education, Kyungpook National University, Daegu, Korea
Corresponding author: Maeng-Kyu Kim Tel +82-53-950-5937 Fax +82-53-955-4235 E-mail kimmk@knu.ac.kr
*The KNHANES 2018 was approved by the Korea Centers for Disease Control and Prevention Institutional Review Board (2018-01-03-P-A).
Received 2023 May 16; Revised 2023 May 30; Accepted 2023 May 31.

Abstract

PURPOSE

Physical activity (PA) improves the metabolic syndrome (MetS) risk. According to a recent revision of the PA guidelines for Americans (2018), healthy adults should participate in PA for >300 min/week for additional health benefits. In addition, it is recommended to participate in resistance exercise (RE) ≥2 days/week. This study aimed to determine whether increasing the PA duration or adding RE is more efficient in improving MetS.

METHODS

Data from the 2016-2018 Korean National Health and Nutrition Examination Survey were used. The logistic regression and general linear models in the complex sample were performed with a sample of 8,662 Korean adults aged 19–65. According to the metabolic equivalent task (MET), PA intensity was categorized as low-(LP; <600 MET-min/week), moderate-(MP; 600-3,000 MET-min/week), and high-level PA (HP;≥3,000 MET-min/week). Furthermore, duration was categorized as high duration (HD) and low duration (LD), while RE was categorized more 2 days/week RE (MR) and less 2 days/week RE (LR).

RESULTS

Compared with LP-LR the MR groups showed a significantly low odds ratio (OR) of MetS (p<.05 respectively), whereas the LR groups had no significant OR (p>.05 respectively). Compared with LP-LD, HP-HD had significantly low OR (p<.05), whereas other groups had no significant OR (p>.05 respectively).

CONCLUSIONS

Frequent RE decreases the OR of MetS and is not dependent on PA intensity. To efficiently reduce the OR of MetS in Korean adults, participating in frequent RE, rather than simply prolonging PA, is recommended; although, increasing PA duration can have positive effect in HP. In terms of the reduction of the MetS, more than 300 min/week of PA is unlikely to achieve additional health benefits.

INTRODUCTION

Metabolic syndrome (MetS) is a complex metabolic disorder charac-terized by excess abdominal obesity, hypertension, high fasting glucose levels, and low high density cholesterol (HDL-C) and high triglyceride (TG) levels and may progress to diseases such as type 2 diabetes mellitus and atherosclerosis [1,2]. A patient with ≥3 metabolic disorders is diag-nosed with MetS [3]. According to the global epidemic of overweight and sedentary lifestyles, the prevalence of MetS increased with a global health problem [4].

It is well known that physical activity (PA) prevents unhealthy weight gain and obesity and improves the risk factors for chronic diseases as well as MetS [5]. PA consists of a variety of activities, including aerobic and resistance exercise (RE), and many studies have been investigated the optimal frequency, intensity, and duration of PA for improving MetS [6-9]. It is known that the risk of MetS may be reduced through aerobic exercise, which is the component of PA, through improving the obesity [10]. Furthermore, RE, one of the PA, also improves the MetS by en-hancing the lipid metabolism [11]. Although there were relatively rare large-scale evidences regarding whether PA and/or RE should be promoted to get beneficial effects on the MetS and its components, it was revealed that combination of aerobic exercise and RE have various positive effects on the individual components of MetS [12].

Interestingly, a recent revision of the PA guidelines for Americans rec-ommends that adults perform at least 150 minutes of moderate-intensity PA and participate for ≥300 minutes to gain more health benefits [13]. However, the beneficial effects for PA over 300 minutes are still unclear. Another recommendation to participate in RE more than twice a week [13]. The skeletal muscles are closely related to insulin resistance, and RE plays an important role in developing them [14]. Improving insulin resistance can prevent various metabolic diseases, and participating in RE can prevent various metabolic diseases [15].

Despite numerous studies on the beneficial effects of aerobic exercise or PA on improving MetS, several issues of PA or RE remain. For exam-ple, racial disparities occur in the prevalence of MetS [16,17]. Most of the studies and guidelines on the importance of the role of PA are mainly from Europe or the United States [13,18,19]. In addition, although few studies have investigated effects of PA and RE on MetS [20,21], the optimal duration of PA and the effects of RE with PA level on MetS have not been fully investigated. However, it is limited to identify the individuals or gender-specific characteristics that may affect their physical activities. Therefore, to examine the role of PA and RE in effect on the MetS, this study used a large-scale and reliable dataset from a national survey con-sist of the questionnaire based on physical movement habit of participants. Thus, this study aimed to determine which is more efficient for improving MetS in Korean adults, increasing the PA duration or adding RE.

METHODS

1. Participants

This study used data from the Korean National Health and Nutrition Examination Survey (KNHANES), which was conducted by the recom-mendations of the World Health Organization (WHO) and with the approval of the institutional review board of the Korea Centers for Disease Control and Prevention [22]. In addition, the statistical data of the KNHANES are representative of South Korea, which is extracted annu-ally by stratified, clustered, and systematic sampling. In this study, the 7th data of the KNHANES, where 24,269 people participated in 576 survey districts nationwide, from 2016 to 2018 were vertically merged and analyzed to increase statistical power. Before analysis, data of individuals who had cardiovascular diseases or cancer did not complete ma-jor surveys, or were pregnant women were excluded. The final data of 8,662 (unweighted cases) participants aged ≥19 and ≤65 years of age and who completed clinical examinations and questions in the KNHANES-related PA were used according to the purpose of this study (Fig. 1). The demographic characteristics of participants are shown in Table 1.

Fig. 1.

Flow diagram of the study participants.

Basic characteristics of study participants in this study according to PA level

2. Research instrument

The sampling frame of the KNHANES used the data from the latest Population and Housing Census available at the time of sampling design. Through this process, the representative samples were collected from South Korean citizens aged ≥1 year, which was the target population. The KNHANES consists of a household member confirmation survey, a health survey, a medical examination survey, and a nutrition survey.

3. Physical activity and resistance exercise

Since 2014, the KNHNS has analyzed the populationʼ s physical activity using Global Physical Activity Questionnaire (GPAQ) to accurately measure and interpret the quantity of physical activity per area (work, travel, and recreation activities) and take into account the intensity of physical activity. In this study, the GPAQ was standardized to measure the PA level of people worldwide. PA was assessed by the metabolic equivalent task (MET)-minutes of GPAQ guideline [23]. During work and at leisure, PA was calculated as the sum of walking, moderate, and vigorous MET-minutes in a week. Walking, moderate, and vigorous MET-minutes were calculated as follows:

  • - Occupational vigorous PA (MET)=8.0×vigorous PA (day/week)×1-day vigorous PA (min/day)

  • - Occupational moderate PA (MET)=4.0×moderate PA (day/week)×1-day moderate PA (min/day)

  • - Recreational vigorous PA (MET)=8.0×vigorous PA (day/week)×1-day vigorous PA (min/day)

  • - Recreational moderate PA (MET)=4.0×moderate PA (day/week)×1-day moderate PA (min/day)

  • - Place movement (MET)=4.0×place movement (day/week)×1-day place movement (min/day)

  • - Total=occupational vigorous PA+occupational moderate PA+ recreational vigorous PA+recreational moderate PA+place movement

The level of PA was classified into three groups based on the WHO guidelines, low-level PA (LP; <600 MET - min/week), moderate-level PA (MP; 600-3,000 MET - min/week), and high-level PA (HP; ≥3,000 MET - min/week). Furthermore, duration was categorized as high duration (HD; ≥300 min PA per week) and low duration (LD; <300 min PA per week), whereas RE was categorized as ≥2 days RE per week (MR) and <2 days RE per week (LR).

4. Metabolic syndrome

According to the National Cholesterol Education Program Adult Treatment Panel Ⅲ [3], the criteria for MetS include waist circumference (WC), blood pressure (BP), fasting glucose, high-density lipoprotein cholesterol (HDL-C), and triglyceride (TG). We used the criterion of the Asia-Pacific Region for WC instead of the original [24]. MetS was defined as the presence of ≥3 of the following components: (i) WC ≥90 cm for men and ≥80 cm for women; (ii) systolic blood pressure (SBP) ≥130 mmHg or diastolic blood pressure (DBP) ≥85 mmHg; (iii) fasting glucose >100 mg/dL; (iv) HDL-C <40 mg/dL for men and <50 mg/dL for women; and (v) TG ≥150 mg/dL.

5. Statistical analysis Metabolic syndrome

All analyses were performed using IBP SPSS for Windows version 25.0 (IBM Corp., Armonk, NY, USA). Because stratified, clustered, and systematic sampling methods were used in KNHANES, sampling weight with complex sample procedures were applied to decrease the bias associated with nonresponse and non-coverage of the population. Logistic regression and general linear model were performed by adjusting for covariates such as sex, age, current smoking status and alcohol use. Statistical significance was considered for p-values <.05.

RESULTS

1. Participant characteristics

Table 1 presents the baseline characteristics of the participants. Among 8,662 participants, 2,229 (27.3%) participated in RE ≥2 days a week, and 5,609 (62.8%) participated in PA for ≥300 minutes per week. Furthermore, 1,346 (14.8%) developed MetS.

Tables 2 and 3 show the differences in MetS and MetS components according to the PA intensity with RE level or PA duration. In Table 2, participants were categorized into six groups based on PA intensity and RE level. Significant differences in MetS prevalence and MetS components, excluding SBP and DBP, were identified. In Table 3, participants were categorized into six groups based on PA intensity and duration. Significant differences in MetS prevalence and WC among MetS components were observed.

Basal characteristics of participants according to the PA level and RE level

Basal characteristics of participants according to the PA level and duration level

2. Effects of physical activity duration and intensity on the metabolic syndrome

The results of the complex samples logistic regression analysis of the MetS prevalence and MetS components according to the PA level and duration are shown in Fig. 2 and Table 4. This model was adjusted by sex, age, current smoking status, and alcohol use. The prevalence of MetS was significantly lower than the baseline values for HP-HD (0.756, 95% confidence interval [CI) 0.597-0.957).

Fig. 2.

Odds ratio of metabolic syndrome according to physical activity level and duration.

LP, low level physical activity; LD, less than 300 minutes physical activity per week; HD, more than 300 minutes physical activity per week; MP, moderate level physical activity; HP, high level physical activity.

Odds ratios (95% CI) for MetS components according to PA and duration level

High TG odds ratio (OR) was significantly reduced for HP-HD (0.810, 95% CI 0.675-0.971). Low HDL-C OR were significantly reduced for MP-HD (0.866, 95% CI 0.756-0.991) and HP-HD (0.757, 95% CI 0.621-0.923).

3. Effects of resistance exercise and physical activity on the metabolic syndrome

The results of the complex samples logistic regression analysis of the MetS prevalence and MetS components according to the PA and RE levels are shown in Fig. 3 and Table 5. This model was adjusted by sex, age, current smoking status, and alcohol use. The prevalence of MetS was significantly lower than the baseline values for MR groups (HP-MR: 0.471, 95% CI: 0.332-0.669; MP-MR: 0.644, 95% CI: 0.509-0.815; LP-MR: 0.581, 95% CI: 0.435-0.776).

Fig. 3.

Odds ratio of metabolic syndrome according to physical activity level with resistance exercise participation.

LP, low level physical activity; LR, less than two days resistance training per week; MR, more than two days resistance training per week; MP, moderate level physical activity; HP, high level physical activity.

Odds ratios (95% CI) for MetS components according to PA and RE level

Large WC OR were significantly reduced for MP-MR (0.492, 95% CI: 0.338-0.715) and LP-MR (0.436, 95% CI 0.278-0.683). High TG (HP-MR: 0.640, 95% CI 0.495-0.827; MP-MR: 0.731, 95% CI 0.604-0.884; LP-MR: 0.658, 95% CI 0.517-0.839) and high glucose OR (HP-MR: 0.766, 95% CI 0.597-0.983; MP-MR: 0.799, 95% CI 0.660-0.966; LP-MR: 0.732, 95% CI 0.581-0.921) were also significantly lower than the baseline values for MR groups. Low HDL-C OR were significantly reduced for MP-MR (0.617, 95% CI 0.509-0.748]) and HP-MR (0.621, 95% CI 0.477-0.809).

DISCUSSION

The KNHANES is a nationally representative survey that provides data on the health and nutritional status of the Korean population. This study investigated the relationship between RE and PA with MetS. The results showed that both RE and PA had a beneficial effect on MetS, with RE having a greater effect.

Significant differences were found between the PA level, RE level, and PA duration in MetS. Except for BP, other MetS components demon-strated significant differences according to the PA and RE levels. However, only the WC showed significant differences according to the PA level and duration. The results of complex samples logistic regression analysis revealed that frequent RE participants showed a significantly decreased MetS risk and risk for some MetS components. Although prolonged PA duration also decreased MetS risk and risk for some MetS components, HP-HD showed a significantly decreased risk of MetS, high TG level, and low HDL-C level, and MP-HD showed a significantly decreased risk of low HDL-C.

Previous studies have reported that PA negatively associated with the prevalence of MetS [25,26]. Recent studies have shown that PA or aerobic exercise can improve various components of MetS, including body composition [27,28], insulin resistance and lipid metabolism [29-31], and cardiovascular function [31,32]. Specifically aerobic exercise reduces chronic inflammation, increases energy expenditure, and increases expression of PGC-1a, which protects against mitochondrial diseases such as apoptosis and oxidative damage [28-31]. Several studies comparing PA intensity and duration in improving metabolic function have been conducted [19,33]; however, studies on the combined effects of PA intensity and duration remain insufficient. Despite the importance of PA intensity, PA duration also plays an important role in reducing the prevalence and risk of MetS. Churilla & Fitzhugh (2012) reported that those who met the recommendation of PA duration have reduced MetS risk, and inves-tigators suggested that not only the intensity but also the duration of PA may affect MetS risk [19]. In the present study, duration does not affect in the LP group; however, in the MP and HP groups, HD improved the MetS components compared with LD. In this respect, for the MetS components, prolonged PA duration appears to be most effective when ac-companied by at least moderate levels of PA intensity.

Although the HP-LD group did not have a significantly low OR, many previous studies have reported that high-intensity PA improves MetS. Laaksonen et al. [18] reported the benefit of high-level PA on the risk of MetS, and Laursen et al. [33] suggested that high-intensity PA is important in reducing MetS. Interestingly, our findings were consistent with those of Johnson et al. [34] who reported that low-volume vigorous-intensity group had no significant improvement in MetS components compared with the inactive group. Similar to the study by Johnson et al. [34] the results of the present study are considered influenced by the effect of low frequency in the HP-LD group or by the large deviation because of the small sample size. Thus, experimental studies analyzing various variables are needed to solve the problem in the future.

RE such as muscular strengthening exercise is an effective strategy for improving muscle mass and strength and improving insulin sensitivity and glycemic control [5,35]. Specifically, increased muscle mass has positive effect on total activity of glycogen synthase, protein content of GLUT4, and AMP-activated protein kinase, which in turn improves lipid metabolism and insulin sensitivity [5,35]. Our findings suggest that the prevalence of MetS among Korean adults in MP or HP is not significantly lower than that of the LP-LR group if they do not participate in RE. According to Bateman et al. [20] performing aerobic and resistance training in combination, rather than performing them alone, was the most effective. Specifically, when only resistance training was performed, only the peak oxygen consumption and strength were significantly increased, and when only aerobic training was performed, only the body mass, peak oxygen consumption, and TG were significantly improved.

However, when aerobic and resistance training were performed in combination, body mass, peak oxygen consumption, strength, TG, WC, and BP were significantly improved [20]. These results appear to be simi-lar to our findings. In this study, TG and glucose were improved in the group that performed the recommended level of RE along with the increase in PA level, and WC and HDL-C were independent of the PA level, but improved when RE was added. This finding is consistent with those of previous studies that reported a negative relationship between muscular strengthening PA and MetS [5,15], which may be due to improved insulin resistance and glycemic control by the involvement of more muscles. This suggests that participation in RE as a long-term strategy to improve the MetS may lead to mechanisms that improve lipid metabolism and consequently reduce the prevalence of MetS. Interestingly one previous study found that men who had significantly reduced physical activity due to the COVID-19 pandemic but continued to participate in RE reported lower rates of abdominal obesity than those who did not participate in RE [36]. These findings are in line with those reported in the present study, where higher RE frequency was associated with protection against MetS even at the level of PA decreased.

This study has some limitations. First, the cross-sectional design prevents the inference of causality. Second, data using questionnaires that have potential recall bias for responses regarding PA patterns may have limited accuracy. Finally, we could not completely rule out the possibility of residual confounding because of unmeasured covariates, such as di-etary factors.

CONCLUSION

In conclusion, participating in frequent RE decreases the OR of MetS prevalence, and it is not dependent on PA intensity. Although the analysis was conducted using a large-scale data set, the proportion of people with high physical activity level was still low. Moreover, while our findings suggest the importance of RE, paradoxically, ratio of participation in RE is insufficient. Therefore, to efficiently reduce the OR of MetS in Korean adults, participation in RE should be actively promoted rather than simply prolonging the PA, although increasing the PA duration can positively affect HP group.

Notes

The authors have no conflicts of interest to declare for this study. This research did not receive any specific grant from any funding agencies in the public, commercial, or not-for-profit sectors.

AUTHOR CONTRIBUTION

Conceptualization: MK Kim; Methodology: MK Kim, HD Jo; Formal analysis: MK Kim, HD Jo; Data Curation: MK Kim, HD Jo; Writing - Original Draft: MK Kim, HD Jo; Writing - Review & Editing: MK Kim, HD Jo.

References

1. . Liese AD, Mayer-Davis EJ, Haffner SM. Development of the multiple metabolic syndrome: an epidemiologic perspective. Epidemiol Rev 1998;20:157–72.
2. . Ardern CI, Janssen I. Metabolic syndrome and its association with morbidity and mortality. Appl Physiol Nutr Metab 2007;32:33–45.
3. . Grundy SM. Third report of the national cholesterol education pro-gram (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) final report. Circulation 2002;106:3143–421.
4. . World Health Organization. Obesity: preventing and managing the global epidemic. World Health Organ Tech Rep Ser 2000;894:1–253.
5. . Lakka TA, Laaksonen DE. Physical activity in prevention and treatment of the metabolic syndrome. Appl Physiol Nutr Metab 2007;32:76–88.
6. . Janssen I, Ross R. Vigorous intensity physical activity is related to the metabolic syndrome independent of the physical activity dose. Int J Epidemiol 2012;41:1132–40.
7. . Clarke J, Janssen I. Is the frequency of weekly moderate-to-vigorous physical activity associated with the metabolic syndrome in Canadian adults? Appl Physiol Nutr Metab 2013;38:773–8.
8. . Jefferis BJ, Parsons TJ, Sartini C, Ash S, Lennon L, et al. Does duration of physical activity bouts matter for adiposity and metabolic syndrome? A cross-sectional study of older British men. Int J Behav Nutr Phys Act 2016;13:1–11.
9. . Powell KE, King AC, Buchner DM, Campbell WW, DiPietro L, et al. The scientific foundation for the physical activity guidelines for Americans. J Phys Act Health 2018;16:1–11.
10. . Okura T, Nakata Y, Ohkawara K, Numao S, Katayama Y, et al. Effects of aerobic exercise on metabolic syndrome improvement in response to weight reduction. Obesity 2007;15:2478–84.
11. . Costa RR, Buttelli ACK, Vieira AF, Coconcelli L, de Lima Magalhães R, et al. Effect of strength training on lipid and inflammatory outcomes: systematic review with meta-analysis and meta-regression. J Phys Act Health 2019;16:477–91.
12. . Wewege MA, Thom JM, Rye K-A, Parmenter BJ. Aerobic, resistance or combined training: a systematic review and meta-analysis of exercise to reduce cardiovascular risk in adults with metabolic syndrome. Atherosclerosis 2018;274:162–71.
13. . Piercy KL, Troiano RP, Ballard RM, Carlson SA, Fulton JE, et al. The physical activity guidelines for Americans. Jama 2018;320:2020–28.
14. . Kelley DE. Skeletal muscle fat oxidation: timing and flexibility are ev-erything. J Clin Investig 2005;115:1699–02.
15. . Green DJ, Maiorana A, O'Driscoll G, Taylor R. Effect of exercise training on endothelium-derived nitric oxide function in humans. J Physiol 2004;561:1–25.
16. . Lear SA, Gasevic D. Ethnicity and metabolic syndrome: Implications for assessment, management and prevention. Nutrients 2019;12:15.
17. . Zhang R, Sun J, Wang C, Wang X, Zhao P, et al. The Racial Disparities in the Epidemic of Metabolic Syndrome With Increased Age: A Study From 28,049 Chinese and American Adults. Front Public Health 2022. 2385.
18. . Laaksonen DE, Lakka H-M, Salonen JT, Niskanen LK, Rauramaa R, et al. Low levels of leisure-time physical activity and cardiorespiratory fitness predict development of the metabolic syndrome. Diabetes care 2002;25:1612–8.
19. . Churilla JR, Fitzhugh EC. Total physical activity volume, physical activity intensity, and metabolic syndrome: 1999-2004 National Health and Nutrition Examination Survey. Metab Syndr Relat Disord 2012;10:70–6.
20. . Bateman LA, Slentz CA, Willis LH, Shields AT, Piner LW, Bales CW, et al. Comparison of aerobic versus resistance exercise training effects on metabolic syndrome (from the Studies of a Targeted Risk Reduction Intervention Through Defined Exercise-STRRIDE-AT/RT). Am J Card 2011;108:838–44.
21. . Bakker EA, Lee D-c, Sui X, Artero EG, Ruize JR, Eijsvogels TM, et al. Association of resistance exercise, independent of and combined with aerobic exercise, with the incidence of metabolic syndrome. Mayo Clin Proc 2017;92:1214–22.
22. . Park J, Park Y, Lee Y, Lee J, Lee S, Shin C, Sung ES. Comparative analysis of energy intake and physical activity according to household type and presence of metabolic syndrome in middle-aged men based on data from the 7th Korea national health and nutrition examination survey (KNHANES)(2016-2018). Phys Act Nutr 2021;25(4):1.
23. . World Health Organization. Global physical activity questionnaire (GPAQ) analysis guide. Geneva: World Health Organ 2012. 1–22.
24. . World Health Organization. The Asia-Pacific perspective: redefining obesity and its treatment 2000.
25. . Petersen CB, Nielsen AJ, Bauman A, Tolstrup JS. Joint association of physical activity in leisure and total sitting time with metabolic syndrome amongst 15,235 Danish adults: a cross-sectional study. Prev Med 2014;69:5–7.
26. . Hastert TA, Gong J, Campos H, Baylin A. Physical activity patterns and metabolic syndrome in Costa Rica. Prev Med 2015;70:39–45.
27. . Rodriguez-Hernandez MG, Wadsworth DW. The effect of 2 walking programs on aerobic fitness, body composition, and physical activity in sedentary office employees. PloS One 2019;14:e0210447.
28. . da Silva MR, Waclawovsky G, Perin L, Camboim I, Eibel B, et al. Effects of high-intensity interval training on endothelial function, lipid profile, body composition and physical fitness in normal-weight and overweight-obese adolescents: a clinical trial. Physiol Behav 2020;213:112728.
29. . Houmard JA, Tanner CJ, Slentz CA, Duscha BD, McCartney JS, et al. Effect of the volume and intensity of exercise training on insulin sensitivity. J Appl Physiol 2004;96:101–6.
30. . Ingelsson E, Ärnlöv J, Sundström J, Risérus U, Michaëlsson K, et al. Rel-ative importance and conjoint effects of obesity and physical inactivity for the development of insulin resistance. Eur J Prev Cardiol 2009;16:28–33.
31. . Muscella A, Stefano E, Marsigliante S. The effects of exercise training on lipid metabolism and coronary heart disease. Am J Physiol Heart Circ Physiol 2020;319:H76–H88.
32. . Huang Z, Chen G, Wang X, Zang Y, Yue Q, et al. The effect of acute aerobic exercise on arterial stiffness in individuals with different body fat percentages: A cross-sectional study. Front Cardiovasc Med 2022;9
33. . Laursen AH, Kristiansen OP, Marott JL, Schnohr P, Prescott E. Intensity versus duration of physical activity: implications for the metabolic syndrome. A prospective cohort study. BMJ Open 2012;2:e001711.
34. . Johnson JL, Slentz CA, Houmard JA, Samsa GP, Duscha BD, et al. Exercise training amount and intensity effects on metabolic syndrome (from Studies of a Targeted Risk Reduction Intervention through Defined Exercise). Am J Card 2007;100:1759–66.
35. . Churilla JR, Johnson TM, Magyari PM, Crouter SE. Descriptive analysis of resistance exercise and metabolic syndrome. Diabetes Metab Syndr 2012;6:42–7.
36. . Park MY, Chung N. Changes in physical activity and energy intake according to abdominal obesity in Korean adult men before and after COVID-19: Data from 2019 and 2020 Korea National Health and Nutrition Examination Survey (KNHANES). Phys Act Nutr 2022;26(3):006–015.

Article information Continued

Fig. 1.

Flow diagram of the study participants.

Table 1.

Basic characteristics of study participants in this study according to PA level

Weighted N Unweighted N % (Weighted)
Sex
  Male 11,463,174.85 3,797 51.2
  Female 10,926,842.89 4,865 48.8
Age
  19-29 5,555,118.43 1,647 24.8
  30-39 4,768,054.92 1,810 21.3
  40-49 5,302,773.36 2,101 23.7
  50-59 4,745,577.79 2,001 21.2
  60-65 2,018,493.24 1,103 9.0
Current smoking status
  Yes 4,924,167.26 1,672 22.0
  No 17,465,850.48 6,990 78.0
Alcohol use
  Yes 21,314,777.41 8,173 95.2
  No 1,075,240.33 489 4.8
Resistance exercise
  less than 2 days 16,274,569.48 6,433 72.7
  more than 2 days 6,115,448.26 2,229 27.3
Physical activity duration
  less than 300 min 8,318,364.25 3,053 37.2
  more than 300 min 14,071,653.49 5,609 62.8
MetS prevalnce 3,311,370.68 1,346 14.8

Data are expressed as mean±SEM. or number(%); columns total 100.

RE, resistance exercise participation per week; DU, physical activity duration per week; MetS, metabolic syndrome.

Table 2.

Basal characteristics of participants according to the PA level and RE level

Low Moderate High p-value
LR (n=2,934) MR (n=664) LR (n=2,875) MR (n=989) LR (n=624) MR (n=576)
Age 42.80±0.29 43.25±0.59 40.51±0.31 39.82±0.50 39.76±0.59# 37.16±0.61*# .000
BMI 23.69±0.09 23.59±0.13 23.90±0.09 23.57±0.12 24.40±0.18 24.24±0.16 .000
HR 70.76±0.23 69.74±0.43 70.39±0.22 69.54±0.37 68.93±0.44# 67.67±0.48# .000
MetS 552 (17.7) 87 (12.7)* 434 (14.5) 127 (12.2) 95 (15.4) 51 (9.0)* .000
WC 80.88±0.24 81.35±0.41 81.10±0.25 80.63±0.35 82.61±0.50# 81.55±0.47 .022
  M≥90, F≥80 321 (9.7) 29 (3.8) 292 (9.0) 43 (4.2) 55 (8.3) 30 (5.3)
SBP 115.15±0.35 114.87±0.57 114.65±0.34 115.73±0.50 116.36±0.64 115.36±0.70 .167
DBP 76.39±0.24 76.05±0.41 76.39±0.24 76.75±0.38 76.78±0.44 76.02±0.47 .677
  SBP≥130, DBP≥85 727 (24.4) 180 (25.5) 711 (25.2) 254 (25.8) 176 (27.8) 132 (24.2)
TG 140.64±3.60 127.92±4.47 132.03±2.44 131.74±4.95 143.30±7.65 115.00±3.70*# .000
  ≥150 869 (29.6) 172 (26.1) 745 (27) 251 (26.1) 170 (29.2) 135 (25)
Glucose 98.99±0.46 95.89±0.56* 96.78±0.41 96.56±0.80 98.96±1.59 95.35±1.01 .001
  >100 923 (30.2) 196 (28.3) 812 (26.6) 271 (25.8) 183 (29.2) 138 (23.8)
HDL-C 51.96±0.26 51.44±0.50 52.55±0.28 53.32±0.46 51.94±0.66 52.99±0.58 .034
  M<40, F<50 929 (29.7) 166 (24.1) 819 (27.6) 200 (18.6) 149 (24.2) 104 (17.2)

Data are expressed as mean±SEM. or number (%); columns total 100%. p-values were obtained from modified F-test or chi-square test.

PA, physical activity; RE, resistance exercise; LR, less than 2 days resistance training per week; MR, more than 2 days resistance training per week; HR, heart rate; MetS, metabolic syndrome; WC, waist circumference; SBP, systolic blood pressure; DBP, diastolic blood pressure; TG, triglyceride; HDL-C, high density lipoprotein cholesterol.

significant differences between Low and Moderate group in same RE level;

significant differences between Low and High group in same RE level;

#

significant differences between Moderate and High group in same RE level;

*

significant differences between LR and MR group in same PA level.

Table 3.

Basal characteristics of participants according to the PA level and duration level

Low Moderate High p-value
LD (n=3,454) HD (n=144) LD (n=2,099) HD (n=1,765) LD (n=56) HD (n=1,144)
Age 42.78±0.26 45.34±1.12 40.34±0.34 40.31±0.38 43.33±1.42 38.26±0.43* # .000
BMI 23.66±0.08 24.08±0.38 23.70±0.09 23.94±0.10 23.74±0.42 24.35±0.13 .000
HR 70.65±0.21 68.50±0.81 70.10±0.25 70.24±0.28 67.63±1.52 68.33±0.35# .000
MetS 609 (16.6) 30 (19.6) 316 (14.2) 245 (13.5) 4 (7.9) 142 (12.4) .003
Waist 80.90±0.22 82.45±0.97 80.79±0.27 81.17±0.29 80.69±1.27 82.14±0.36 .018
  M ≥90, F ≥80 337 (8.6) 13 (7.7) 192 (8.3) 143 (7.1) 1 (1.4) 84 (7.0)
SBP 115.01±0.31 117.15±1.34 114.40±0.37 115.57±0.40 116.52±2.26 115.83±0.49 .057
DBP 76.24±0.21 78.32±1.09 76.20±0.26 76.82±0.29 78.14±1.42 76.33±0.33 .148
  SBP ≥130, DBP ≥85 861 (24.4) 46 (30.4) 513 (24.7) 452 (26.1) 13 (25.0) 295 (26.0)
TG 137.96±3.10 143.54±10.50 130.41±2.88 133.71±3.39 198.22±54.34 126.31±3.95 .095
  ≥150 995 (28.8) 46 (30.8) 530 (26.5) 266 (27.1) 13 (25.7) 292 (27.2)
Glucose 98.21±0.39 102.66±2.98 96.38±0.44 97.11±0.61 100.03±3.35 97.04±1.03 .059
  >100 1069 (29.6) 50 (35.0) 582 (26.1) 501 (26.7) 19 (36.3) 302 (26.1)
HDL-C 51.92±0.25 50.49±1.14 52.93±0.31 52.55±0.34 50.59±2.03 52.54±0.45 .058
  M <40, F <50 1052 (28.7) 43 (28.0) 563 (25.8) 456 (24.5) 12 (27.6) 241 (20.5)

Data are expressed as mean±SEM. or number (%); columns total 100%. p-values were obtained from modified F-test or chi-square test.

PA, physical activity, LD, less than 300 minutes physical activity per week; HD, more than 300 minutes physical activity per week; HR, heart rate; MetS, metabolic syndrome; WC, waist circumference; SBP, systolic blood pressure; DBP, diastolic blood pressure; TG, triglyceride; HDL-C, high density lipoprotein cholesterol.

significant differences between Low and Moderate group in same duration level;

significant differences between Low and vigorous group in same duration level;

#

significant differences between Moderate and Vigorous group in same duration level;

*

significant differences between LD and HD group in same intensity level.

Fig. 2.

Odds ratio of metabolic syndrome according to physical activity level and duration.

LP, low level physical activity; LD, less than 300 minutes physical activity per week; HD, more than 300 minutes physical activity per week; MP, moderate level physical activity; HP, high level physical activity.

Table 4.

Odds ratios (95% CI) for MetS components according to PA and duration level

Large WC Hypertension High TG High glucose Low HDL-C
LP-LD 1.00 (reference) 1.00 (reference) 1.00 (reference) 1.00 (reference) 1.00 (reference)
LP-HD 1.040 (0.540-2.006) 0.998 (0.640-1.556) 0.823 (0.538-1.260) 0.930 (0.602-1.436) 1.015 (0.682-1.511)
MP-LD 0.983 (0.786-1.228) 1.128 (0.964-1.321) 0.939 (0.806-1.094) 0.949 (0.814-1.107) 0.907 (0.795-1.034)
MP-HD 0.886 (0.700-1.121) 0.154 (0.981-1.358) 0.902 (0.778-1.046) 0.943 (0.811-1.097) 0.866* (0.756-0.991)
HP-LD 0.182 (0.025-1.306) 0.842 (0.409-1.731) 0.660 (0.321-1.355) 1.203 (0.614-2.354) 1.042 (0.499-2.177)
HP-HD 1.017 (0.762-1.359) 1.091 (0.892-1.333) 0.810* (0.675-0.971) 0.926 (0.769-1.116) 0.757** (0.621-0.923)

Data are expressed as odds ratio (95% confidence intervals [CIs]).

WC, waist circumference; TG, triglyceride; HDL-C, high density lipoprotein cholesterol; LD, less than 300 minutes physical activity per week; HD, more than 300 minutes physical activity per week; LP, low level physical activity; MP, moderate level physical activity; HP, high level physical activity.

* p<.05, ** p<.01 vs. reference. The model was adjusted for sex, age, current smoking status, alcohol use.

Fig. 3.

Odds ratio of metabolic syndrome according to physical activity level with resistance exercise participation.

LP, low level physical activity; LR, less than two days resistance training per week; MR, more than two days resistance training per week; MP, moderate level physical activity; HP, high level physical activity.

Table 5.

Odds ratios (95% CI) for MetS components according to PA and RE level

Large WC Hypertension High TG High glucose Low HDL-C
LP-LR 1.00 (reference) 1.00 (reference) 1.00 (reference) 1.00 (reference) 1.00 (reference)
LP-MR 0.436** (0.278-0.683) 0.836 (0.668-1.046) 0.658)** (0.517-0.839 0.732** (0.581-0.921) 0.819 (0.658-1.020)
MP-LR 0.962 (0.786-1.176) 1.133 (0.976-1.315) 0.907 (0.789-1.044) 0.931 (0.807-1.073) 0.948 (0.845-1.064)
MP-MR 0.492** (0.338-0.715) 1.014 (0.833-1.234) 0.731** (0.604-0.884) 0.799* (0.660-0.966) 0.617** (0.509-0.748)
HP-LR 0.998 (0.701-1.422) 1.160 (0.905-1.486) 0.852 (0.681-1.067) 0.999 (0.793-1.258) 0.849 (0.666-1.083)
HP-MR 0.723 (0.461-1.134) 0.920 (0.716-1.182) 0.640** (0.495-0.827) 0.766* (0.597-0.983) 0.621** (0.477-0.809)

Data are expressed as odds ratio (95% confidence intervals [CIs]).

WC, waist circumference; TG, triglyceride; HDL-C, high density lipoprotein cholesterol; LR, less than 2 days resistance training per week; MR, more than 2 days resistance training per week; LP, low level physical activity; MP, moderate level physical activity; HP, high level physical activity

*p<.05, **p<.01 vs. reference. The model was adjusted for sex, age, current smoking status, alcohol use.