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Article

Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women

by
Jin-Suk Ra
1 and
Hyesun Kim
2,*
1
College of Nursing, National University, Daejeon 35015, Korea
2
Department of Nursing, National University Hospital, Chungbuk 28644, Korea
*
Author to whom correspondence should be addressed.
Healthcare 2021, 9(7), 848; https://doi.org/10.3390/healthcare9070848
Submission received: 24 May 2021 / Revised: 1 July 2021 / Accepted: 2 July 2021 / Published: 5 July 2021
(This article belongs to the Special Issue Diagnosis and Treatment for Women's Health)
Versions Notes

Abstract

:
This study aimed to identify the combined effects of unhealthy lifestyle behaviors, including diet, sedentary behavior, and physical activity on metabolic syndrome (MS) and components of MS among postmenopausal women. Secondary data analysis was conducted using the Korean National Health and Nutrition Examination Survey (2014–2018) with a cross-sectional study design. Logistic regression analysis was conducted with data from 6114 Korean postmenopausal women. While no significant effects of unhealthy lifestyle behaviors, either individually or as a combination, were found for MS, prolonged sedentary behavior without poor dietary behavior and insufficient physical activity was associated with increased likelihood of abdominal obesity (adjusted odds ratio [AOR]: 1.59, 95% confidence interval [CI]: 1.10–2.29) and impaired fasting glucose (AOR: 1.54, 95% CI: 1.13–2.10). The combination of poor dietary behavior and prolonged sedentary behaviors was also associated with increased likelihood of abdominal obesity (AOR: 1.48, 95% CI: 1.10–2.00) and impaired fasting glucose (AOR: 1.49, 95% CI: 1.14–1.96). In addition, prolonged sedentary behavior and insufficient physical activity together were associated with increased likelihood of abdominal obesity (AOR: 2.81, 95% CI: 1.90–4.20) and impaired fasting glucose (AOR: 1.59, 95% CI: 1.13–2.24). Finally, combining poor dietary behavior, prolonged sedentary behavior, and insufficient physical activity was also associated with increased likelihood of abdominal obesity (AOR: 2.05, 95% CI: 1.50–2.80) and impaired fasting glucose (AOR: 1.71, 95% CI: 1.32–2.23). Strategies for replacing sedentary behavior of postmenopausal women with activities are warranted for prevention of abdominal obesity and impaired fasting glucose.

1. Introduction

Metabolic syndrome (MS) is a cluster of cardiovascular and metabolic risk factors, which includes elevated blood pressure, abdominal (visceral) obesity, altered lipid metabolism, and impaired glucose levels. The development of MS has been associated with increased age and unhealthy lifestyle behaviors, such as poor dietary behavior (e.g., excessive intake of calories), prolonged sedentary behavior, and insufficient physical activity [1]. According to the national data of the United States of America, between 2011 and 2016, 34.7%–50.4% of adults aged 40 to 60 years had MS; in contrast, the prevalence of MS was 16.2%–21.3% in those aged 20 to 39 years [2]. In Korea, 30%–40% of adults aged over 40 years had MS between 2013 and 2015 [3]. Thus, this syndrome may be a significant health problem among middle-aged and older individuals.
Previous studies have reported that the prevalence of MS was greater among middle-aged and older women than men of the same age [4,5]. Moreover, an increased prevalence of MS may be associated with menopause among middle-aged and older women [5,6]. Menopause promotes abdominal obesity with changes in body fat distribution, which is associated with an increased risk of insulin resistance, dyslipidemia, and hypertension [6,7,8]. In the same vein, a previous study reported that postmenopausal women had a greater risk of type 2 diabetes mellitus (T2DM), low high-density lipoprotein (HDL) cholesterol, high low-density lipoprotein (LDL) cholesterol levels, and hypertension [9,10]. Hence, postmenopausal women are considered high-risk individuals for MS and its complications, such as cardiovascular diseases (CVDs).
An increased risk of MS is associated with unhealthy lifestyle behaviors, including poor dietary behaviors, prolonged sedentary behaviors, and insufficient physical activity [11,12,13]. Since dietary intake and physical activity are major variables in our daily lives, these are also significant determinants of MS and components of MS such as waist circumference, blood pressure, HDL cholesterol, triglyceride, and fasting blood sugar [12,13,14,15]. According to a study by Myers et al. [16], sufficiently increased physical activity was effective for prevention and management of MS and components of MS, including abdominal obesity and insulin resistance. Similarly, a high calorie diet, prolonged sedentary behaviors, and insufficient physical activity might be independently associated with an increased prevalence of MS in women aged 30 years and above, with sex differences on the impact of lifestyle factors [11,12,13].
However, individuals tend to combine lifestyle factors, with a cluster of specific patterns of lifestyle behaviors [17]. Furthermore, the combined effects of lifestyle behaviors may be different from the independent effect of each lifestyle behavior [18]. The combined effect of lifestyle behaviors on health may be neutralized or reinforced owing to a synergistic effect between the behaviors [19]. Previous studies have shown that combining the effects of sufficient physical activity and healthy dietary habits was significantly better for relieving the risk of MS (e.g., abdominal obesity, high fasting blood sugar) than their individual effects [20]. On the other hand, combining unhealthy lifestyle behaviors was more associated with increased risk of MS than with the sum of the risk of MS associated with each of the individual unhealthy lifestyle behaviors (e.g., poor dietary behaviors, insufficient physical activity) [21]. Postmenopausal middle-aged women showed decreased physical activity with increasing age [22], and their energy intake was higher than that of the other age groups of women and men of the same age [23]. In addition, a modernized lifestyle, prolonged sedentary behaviors and decreased sufficient physical activity resulted in greater risk of MS [24]. Thus, it is necessary to evaluate the potential combined effects of diet, sedentary behavior, and physical activity on MS and components of MS in postmenopausal women. However, we found that there are limited reports on this association in postmenopausal women.
The biopsychosocial model proposed by Hoffman and Driscoll [25] may provide a framework for considering the effects of various covariates for MS, including biomedical factors (e.g., biological process and genetics), biosocial factors (e.g., sex, race/ethnicity, environmental characteristics such as education, socioeconomic status), and psychosocial factors, including emotional status and health-related behaviors (e.g., mood and behaviors) [26]. Based on a literature review following this model, the biomedical factors including age, body mass index (BMI), and family history of hypertension, type 2 diabetes mellitus (T2DM), CVDs, and dyslipidemia, were considered as covariates [5,27,28,29]. Family socioeconomic status and educational level were included as biosocial factors [30,31]. Finally, psychosocial factors such as stress, depression, current or past smoking history, current binge alcohol consumption, and sleep duration were included [29,31]. Thus, the combined effects of unhealthy lifestyle behaviors (poor dietary behavior, prolonged sedentary behavior, and insufficient physical activity) on MS and components of MS among postmenopausal women were identified by controlling the covariates of biomedical, biosocial, and psychosocial factors.

2. Materials and Methods

2.1. Design and Participants

In this cross-sectional study, the secondary data of the 2014–2018 Korean National Health and Nutrition Examination Survey (KNHNES) were analyzed. In most Korean women, menopause occurs after the age of 40 [32]. Among the 39,199 women who participated in the KNHNES, 12,764 women aged >40 years were selected. In addition, among the selected 12,764 women, 6650 women, including 2823 who were premenopausal and 3827 who did not complete a questionnaire assessing health and nutritional status, were excluded. Finally, 6114 women were eligible for the study for data analysis.

2.2. Measurements

2.2.1. Outcome Variable

Metabolic Syndrome

MS was defined in accordance with the diagnostic criteria of the American Heart Association and the National Heart, Lung, and Blood Institute (AHA/NHLBI) [1]. For abdominal obesity in Korean women, waist circumference was evaluated according to criteria suggested by the Korean Society for the Study of Obesity, which reflected optimal waist circumference predicting MS of Korean women [33]. Among the five components for the diagnosis of MS, individuals with three and more components were considered to have MS. The diagnostic criteria were as follows: (i) abdominal obesity: ≥85 cm; (ii) elevated blood pressure: ≥130/85 mmHg or on anti-hypertensive medications; (iii) low HDL cholesterol levels: <50 mg/dL or on anti-dyslipidemic medications; (iv) high triglycerides levels: ≥150 mg/dL or on anti-dyslipidemic medications; and (v) impaired fasting glucose levels: ≥100 mg/dL or on anti-diabetic medications.

2.2.2. Unhealthy Lifestyle Behaviors

Dietary Behavior

Dietary behavior associated with MS was evaluated using the following criteria [21]: (i) >125% of the estimated daily total calorie requirement; (ii) >75% of the recommended daily total intake calories from carbohydrates; (iii) >30% of recommended daily total intake calories from fat; (iv) >130% of the recommended mean sodium intake per day for Koreans. Individuals with more than one dietary criterion among the four were considered to have poor dietary behavior predominantly associated with MS.

Sedentary Behavior

Sedentary behavior was measured using a single question: “How many hours do you usually sit or lie down a day?” Responses were categorized into <8 h a day and ≥8 h a day; sedentary time of more than 8 h a day was considered as prolonged sedentary behavior according to the guidelines of the United Kingdom Chief Medical Officers [34].

Physical Activity

Physical activity was quantified using the Metabolic Equivalent of Task (MET)-minutes of Global Physical Activity Questionnaire (GPAQ) analysis guide (version 2.0) [35]. Physical activity included activities during work, transport, and recreation. This was computed as the sum of transport-related walking or cycling, as well as moderate and vigorous activities in a usual week, measured as metabolic equivalents. Physical activity based on total MET-min/week was categorized as sufficient physical activity (≥600 MET-min/week) and insufficient physical activity (<600 MET-min/week) in accordance with the WHO guideline [35].

2.2.3. Covariates

Biomedical Factors

Age was divided into two categories (40–64 years and ≥65 years). BMI was computed from objectively measured weight and height, and it was divided into two categories (underweight and normal weight (<23 kg/m2); overweight and obese (≥23 kg/m2)) [36]. Family history of hypertension, T2DM, CVDs, dyslipidemia was evaluated using questions on the history of hypertension, T2DM, CVDs, and dyslipidemia to direct family members. The response was either “yes” or “no”.

Biosocial Factors

The highest level of educational attainment was considered the participant’s level of education. The responses were categorized into four groups (lower than elementary school education, graduation from middle school, graduation from high school, college education or above). The socioeconomic status of the family was determined using the level of family income. The responses were categorized into three groups (high, middle, or low).

Psychosocial Factors

Stress was measured using a single question: “How much stress do you feel in your daily life?”. The respondents were categorized as being under severe stress or a little stress or not at all under stress. Depression was evaluated using a single question: “Do you have depression diagnosed by a psychiatrist?”. Current or past smoking history was assessed using a single question on current or past smoking experiences. Responses were categorized into “yes” or “no”. Current binge alcohol consumption was screened with the Alcohol Use Disorders Identification Test Alcohol Consumption Questions (AUDIT-C) that include three questions (amount and frequency of alcohol consumption and frequency of heavy drinking). The total score ranged from 0 to 12 points, with 0 to 4 points being the response rate of each item. More than six points was considered as binge alcohol consumption, based on the criteria proposed by Woo and his colleagues [37]. Sleep duration was divided into two groups, less than 7 h and more than 7 h according to the results of the meta-analysis [38].

2.3. Data Analysis

Data analyses were conducted using complex simple analysis procedures of SPSS version 24.0 (IBM, Armonk, NY, USA) using the guide for data analysis proposed by the Korean National Health and Nutrition Examination Survey. The characteristics of MS, dietary behavior, sedentary behavior, physical activity, and covariates (biomedical, biosocial, and psychosocial factors) were described using frequencies and percentages. Logistic regression analysis was conducted to adjust for covariates, in order to identify the combined effects of unhealthy lifestyle behaviors (poor dietary behavior, prolonged sedentary behavior, and insufficient physical activity) on MS and components of MS among postmenopausal women.

3. Results

3.1. Characteristics of Metabolic Syndrome, Unhealthy Lifestyle, Covariates among Participants

In total, 45.7% of the participants had MS. The prevalence of the five individual MS components is presented in Table 1. Among the total participants, 39.5% had at least one of the three unhealthy lifestyle behaviors associated with MS, namely, poor dietary behavior, prolonged sedentary behavior, or insufficient physical activity; 36.8% of the participants had two of the three unhealthy lifestyle behaviors associated with MS; and 14.5% of the participants had all three unhealthy lifestyle behaviors. Table 1 shows the prevalence of the covariates, including biomedical, biosocial, and psychosocial factors.

3.2. Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome

No significant effects of unhealthy lifestyle behaviors, either individually or as a combination of two or more, were found for MS, after adjusting for covariates (Table 2). However, prolonged sedentary behavior, but not poor dietary behavior or insufficient physical activity, was associated with an increased likelihood of abdominal obesity (adjusted odds ratio [AOR]: 1.59, 95% confidence interval [CI]: 1.10–2.29) and impaired fasting glucose levels (AOR: 1.54, 95% CI: 1.13–2.10). A combination of poor dietary behavior and prolonged sedentary behavior was associated with an increased likelihood of abdominal obesity (AOR: 1.48, 95% CI: 1.10–2.00) and impaired fasting glucose levels (AOR: 1.49, 95% CI: 1.14–1.96). Likewise, a combination of prolonged sedentary behavior and insufficient physical activity was associated with an increased likelihood of abdominal obesity (AOR: 2.81, 95% CI: 1.90–4.20) and impaired fasting glucose levels (AOR: 1.59, 95% CI: 1.13–2.24). Furthermore, a combination of poor dietary behavior, prolonged sedentary behavior, and insufficient physical activity also increased the likelihood of abdominal obesity (AOR: 2.05, 95% CI: 1.50–2.80) and impaired fasting glucose levels (AOR: 1.71, 95% CI: 1.32–2.23).

4. Discussion

This study identified the combined effects of poor dietary behavior, prolonged sedentary behavior, and insufficient physical activity on MS, and components of MS among postmenopausal women. According to the results of the study, postmenopausal women with prolonged sedentary behavior, not including poor dietary behavior and insufficient physical activity, had an increased likelihood of abdominal obesity and impaired fasting glucose levels. Moreover, abdominal obesity and impaired fasting glucose levels were prevalent among postmenopausal women with prolonged sedentary behavior, combined with poor dietary behavior and/or insufficient physical activity. However, despite having healthy dietary patterns and/or doing sufficient physical activity, postmenopausal women with prolonged sedentary behavior might be at risk for abdominal obesity and impaired fasting glucose levels. Thus, prolonged sedentary behaviors might be primarily significant factors associated with metabolic abnormalities of abdominal obesity and impaired fasting glucose with combined poor dietary behaviors and/or insufficient physical activity.
During the normal aging process, postmenopausal women may be at an increased risk of abdominal obesity owing to estrogen deficiency due to decreased ovarian function. During the premenopausal period, sufficient estrogen levels activate lipoproteins (leading to accumulation of fat as energy stores for reproduction) in the femoral adipose tissue rather than in the abdominal adipocytes [39]. Thus, body fat usually tends to accumulate in the femoral region, rather than in the abdomen among premenopausal women [39]. Meanwhile, postmenopausal women with estrogen deficiency may experience a higher accumulation of visceral fat in the abdomen and a lower accumulation of subcutaneous fat in the femoral region [9,40], than those without estrogen deficiency.
Furthermore, postmenopausal women tend to have increased sedentary behavior due to decreased muscle strength and endurance for physical activity, with aging [41]. Prolonged sedentary behavior may lead to decreased energy expenditure due to a lack of physical activity [15]. Moreover, a sedentary behavior, such as working on the computer and TV watching may be associated with an increased energy intake as it encourages snacking [42]. Thus, in postmenopausal women, due to a decreased basal metabolic rate and advancing age, prolonged sedentary behavior leads to a positive energy balance by decreasing energy expenditure and increasing energy intake. Sedentary behavior includes waking activities requiring a resting level of energy expenditure (1.0~1.5 basal metabolic rate), such as sitting (e.g., TV watching) and reclining posture [43]. According to previous studies that objectively measured sedentary behaviors, prolonged sedentary behavior was associated with a greater waist circumference [44,45]. In a systematic review, prolonged sedentary time was associated with a greater waist circumference in those aged 60 years or more [46]. Bankoski and colleagues [30] reported that regardless of the physical activity, the association between objectively measured sedentary time and waist circumference was significantly positive with controlled covariates (sex, age, ethnicity, BMI, smoking, and alcohol consumption). Hence, a decrease in sedentary behavior was recommended for alleviating the risk of abdominal obesity, which is a component of MS [30]. Based on these previous results, an increased risk of abdominal obesity among postmenopausal women may be associated with the additional deleterious effects of extended sedentary behavior and the normal aging process after menopause. In addition, minimizing sedentary behavior may be the primary intervention needed to prevent abdominal obesity among postmenopausal women.
Furthermore, the increased body fat and visceral fat of postmenopausal women with normal aging results in an altered expression of adiponectin, which is involved in the regulation of insulin sensitivity, resulting in increased insulin resistance [47]. Furthermore, increased insulin resistance with menopause may be associated with a predilection to sedentary behavior with advancing age [48]. Similarly, self-reported sedentary time was associated with insulin resistance among older adults without T2DM [49]. A previous study involving middle-aged women in The Netherlands found that women with impaired glucose tolerance and T2DM reported an increased sedentary time of up to 26 min per day when compared to women with normal glucose levels, independent of physical activity [50]. Furthermore, as a major leisure-time sedentary behavior, TV watching time was positively associated with the prevalence of T2DM in women, independent of the physical activity [51]. Similarly, among women without diagnosed diabetes, a dose–response relationship was reported between TV watching time and fasting and 2-h serum glucose levels, after controlling for physical activity and waist circumference [52]. Dunstan et al. [52] proposed that sedentary behavior, including TV watching, is a significant lifestyle behavior that disrupts normal metabolic function, independent of physical activity. Thus, along with healthy dietary behavior and sufficient physical activity, prolonged sedentary behavior needs to be reduced for the prevention of insulin resistance, which is associated with impaired glucose tolerance and T2DM. For individuals with more than 9 h of sedentary time per day, regularly performed light activity (walking for 30 min) which interrupts sedentary behaviors was effective in lowering glucose levels after meals [53]. In addition, Yates and colleagues [54] proposed that replacing 30 min of sedentary behavior with light movement increased insulin sensitivity by 5% among individuals with a high risk of T2DM. Thus, sedentary behavior needs to be replaced with at least light physical activity, in order to maintain normal glucose levels in postmenopausal women.
In our results, the unhealthy lifestyle behaviors were not associated factors on MS among postmenopausal women. According to a previous study of Asians aged above 60 years, poor dietary behaviors such as excessive carbohydrate intake was not associated with MS, and the association between physical activity and MS was inconsistent according to sex [14]. Thus, association between the unhealthy lifestyle behaviors and MS might be influenced by the biological background of individuals, such as sex and race/ethnicity. In addition, association between the unhealthy lifestyle behaviors and MS might be controlled by strong covariates, such as age and BMI. According to Serrano-Sánchez et al. [55], age and BMI had an explanation power of 45.1% and 34.3%, respectively, while that of physical activity was 10%. In addition, a combination of regular physical activity and healthy diet in managing BMI was primarily recommended to decrease the risk of MS [56].
With a large sample size, this study verified the important effects of prolonged sedentary behavior including abdominal obesity and impaired fasting glucose levels, in postmenopausal women. However, this study had several limitations. First, this study used a cross-sectional study design, which does not verify the causal relationship between independent and outcome variables; thus, longitudinal studies are required. Second, the unhealthy lifestyle behaviors were assessed using a self-reported questionnaire; thus, subjective evaluation can be under- or overestimated following social desirability, in comparison to objective measurements. Hence, associations between objectively measured unhealthy lifestyle behaviors and MS need to be verified in future studies. Third, the study included only Korean postmenopausal women. However, patterns of unhealthy lifestyle behaviors associated with MS would differ according to the socio-cultural background of the participants. Thus, a similar study with samples from various cultures is warranted. Fourth, for a combination of unhealthy lifestyle behaviors associated with MS, poor dietary behavior, prolonged sedentary behavior, and insufficient physical activity were selected. Hence, further studies combining other unhealthy lifestyle behaviors associated with MS, such as smoking and alcohol consumption are necessary. Fifth, waist circumference was used as a surrogate marker for abdominal (visceral) obesity; however, since it is an indirect measurement, it is necessary to evaluate this aspect using a more objective and direct measurement (e.g., ultrasonography) in future studies. Sixth, although there are various diagnostic criteria for MS (e.g., International Diabetes Federation, National Cholesterol Education Program-Adult Treatment Panel III, AHA/NHLBI), we used the AHA/NHLBI criteria for diagnosis of MS, which are the most commonly used criteria worldwide. Thus, when different diagnostic criteria are used for MS, the results (e.g., prevalence of MS) may differ from our results, so care must be taken in the interpretation of our results.

5. Conclusions

Estrogen is a critical hormonal regulator involved in the development and deposition of adipose tissue. Deficiency of estrogen due to menopause among women induces greater visceral fat, which is associated with abnormal glucose metabolism (e.g., increased insulin resistance and glucose production in the liver and muscle, decreased insulin secretion in the pancreas) [57]. Thus, postmenopausal women might experience abdominal obesity and hyperglycemia. According to the results of this study, prolonged sedentary behavior has a more important role in abdominal obesity and impaired fasting glucose in postmenopausal women than poor dietary behavior and insufficient physical activity. Thus, in addition to estrogen replacement, interventions for decreasing sedentary behavior should be primarily recommended to prevent abdominal obesity and hyperglycemia among postmenopausal women. Healthcare providers, therefore, should develop strategies for replacing sedentary behavior with activities that involve sufficient movements.

Author Contributions

Conceptualization, J.-S.R.; Methodology, H.K.; Formal Analysis, H.K.; Investigation, J.-S.R.; Writing—Original Draft Preparation, J.-S.R.; Writing—Review and Editing, J.-S.R. and H.K.; Supervision, J.-S.R.; Funding Acquisition, J.-S.R. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by research funding from Chungnam National University. (2021-0756-01).

Institutional Review Board Statement

Since this was a retrospective study and secondary data were used, the institutional review board (IRB) exempted this study from review and approved it (IRB no. 202012-SB-167-01).

Informed Consent Statement

Not applicable.

Data Availability Statement

Data were obtained from KDCA and are available from https://knhanes.kdca.go.kr/knhanes/main.do (accessed on 3 September 2020).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Grundy, S.M.; Cleeman, J.I.; Daniels, S.R.; Donato, K.A.; Eckel, R.H.; Franklin, B.A.; Gordon, D.J.; Krauss, R.M.; Savage, P.J.; Smith, S.C.; et al. Diagnosis and management of the metabolic syndrome. Circulation 2005, 112, 2735–2752. [Google Scholar] [CrossRef] [Green Version]
  2. Hirode, G.; Wong, R.J. Trends in the prevalence of metabolic syndrome in the United States, 2011–2016. JAMA 2020, 323, 2526–2528. [Google Scholar] [CrossRef]
  3. Huh, J.H.; Kang, D.R.; Jang, J.-Y.; Shin, J.-H.; Kim, J.Y.; Choi, S.; Cho, E.J.; Park, J.-S.; Sohn, I.S.; Jo, S.-H.; et al. Metabolic syndrome epidemic among Korean adults: Korean survey of cardiometabolic syndrome. Atherosclerosis 2018, 277, 47–52. [Google Scholar] [CrossRef]
  4. Aguilar, M.; Bhuket, T.; Torres, S.; Liu, B.; Wong, R.J. Prevalence of the metabolic syndrome in the United States, 2003–2012. JAMA 2015, 313, 1973–1974. [Google Scholar] [CrossRef]
  5. Park, E.; Kim, J.S. Gender- and age-specific prevalence of metabolic syndrome Korean adults: Analysis of the fifth Korean National Health and Nutrition Examination Survey. J. Cardiovasc. Nurs. 2015, 30, 256–266. [Google Scholar] [CrossRef]
  6. Bentley-Lewis, R.; Koruda, K.; Seely, E.W. The metabolic syndrome in women. Nat. Clin. Pr. Endocrinol. Metab. 2007, 3, 696–704. [Google Scholar] [CrossRef] [PubMed]
  7. Carr, M.C.; Brunzell, J.D. Abdominal obesity and dyslipidemia in the metabolic syndrome: Importance of type 2 diabetes and familial combined hyperlipidemia in coronary artery disease risk. J. Clin. Endocrinol. Metab. 2004, 89, 2601–2607. [Google Scholar] [CrossRef] [Green Version]
  8. Tangvarasittichai, S.; Pongthaisong, S.; Meemark, S.; Tangvarasittichai, O. Abdominal obesity associated with elevated serum butyrylcholinesterase activity, insulin resistance and reduced high density lipoprotein-cholesterol levels. Indian J. Clin. Biochem. 2014, 30, 275–280. [Google Scholar] [CrossRef] [Green Version]
  9. Carr, M.C. The emergence of the metabolic syndrome with menopause. J. Clin. Endocrinol. Metab. 2003, 88, 2404–2411. [Google Scholar] [CrossRef]
  10. Mainini, G.; Torella, M.; Di Donna, M.C.; Esposito, E.; Ercolano, S.; Correa, R.; De Franciscis, P. Nonhormonal management of postmenopausal women: Effects of a red clover based isoflavones supplementation on climacteric syndrome and cardiovascular risk serum profile. Clin. Exp. Obstet. Gynecol. 2013, 40, 337–341. [Google Scholar]
  11. Hattori, T.; Konno, S.; Munakata, M. Gender differences in lifestyle factors associated with metabolic syndrome and preliminary metabolic syndrome in the general population: The Watary Study. Intern. Med. 2017, 56, 2253–2259. [Google Scholar] [CrossRef] [Green Version]
  12. Kang, Y.; Kim, J. Gender difference on the association between dietary patterns and metabolic syndrome in Korean population. Eur. J. Nutr. 2016, 55, 2321–2330. [Google Scholar] [CrossRef]
  13. Wagner, A.; Dallongeville, J.; Haas, B.; Ruidavets, J.B.; Amouyel, P.; Ferrières, J.; Arveiler, D. Sedentary behaviour, physical activity and dietary patterns are independently associated with the metabolic syndrome. Diabetes Metab. 2012, 38, 428–435. [Google Scholar] [CrossRef]
  14. Johari, S.M.; Shahar, S. Metabolic syndrome: The association of obesity and unhealthy lifestyle among Malaysian elderly people. Arch. Gerontol. Geriatr. 2014, 59, 360–366. [Google Scholar] [CrossRef]
  15. Hamilton, M.T.; Healy, G.N.; Dunstan, D.W.; Zderic, T.W.; Owen, T. Too little exercise and too much sitting: Inactivity physiology and the need for new recommendations on sedentary behavior. Curr. Cardiovasc. Risk Rep. 2008, 2, 292–298. [Google Scholar] [CrossRef] [Green Version]
  16. Myers, J.; Kokkinos, P.; Nyelin, E. Physical activity, cardiorespiratory fitness, and the metabolic syndrome. Nutrients 2019, 11, 1652. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Institute of Medicine, Health and Behavior. The Interplay of Biological, Behavioral and Social Influences; National Academy Press: Washington, DC, USA, 2001. [Google Scholar]
  18. Schuit, A.; van Loon, A.M.; Tijhuis, M.; Ocké, M.C. Clustering of lifestyle risk factors in a general adult population. Prev. Med. 2002, 35, 219–224. [Google Scholar] [CrossRef] [PubMed]
  19. Kang, K.; Sung, J.; Kim, C. High risk groups in health behavior defined by clustering of smoking, alcohol, and exercise habits: National Health and Nutrition Examination Survey. J. Prev. Med. Public Health 2010, 43, 73–83. [Google Scholar] [CrossRef]
  20. Malakou, E.; Linardakis, M.; Armstrong, M.E.G.; Zannidi, D.; Foster, C.; Johnson, L.; Papadaki, A. The combined effect of promoting the Mediterranean diet and physical activity on metabolic risk factors in adults: A systematic review and meta-analysis of randomised controlled trials. Nutrients 2018, 10, 1577. [Google Scholar] [CrossRef] [Green Version]
  21. Lee, J.A.; Cha, Y.H.; Kim, S.H.; Park, H.S. Impact of combined lifestyle factors on metabolic syndrome in Korean men. J. Public Health 2017, 39, 82–89. [Google Scholar] [CrossRef]
  22. Kim, J.H.; Jung, I.K. Relationship among physical activities, nutrient intake, and health-related factors in menopausal women: Based on 6th (2014) Korean national health and nutrition examination survey (KNHANES). J. Korean Assoc. Phys. Educ. Sport Girls Women. 2016, 30, 237–252. [Google Scholar] [CrossRef]
  23. Cho, W.J. The comparison of physical activity habit and nutritional status of middle aged adults by physical activity level in men and women in Korean. J. Korean Soc. Wellness 2019, 14, 509–518. [Google Scholar] [CrossRef]
  24. Kwon, H.K.; Ha, C.D.; Kang, H.S. Effects of sedentary behavior modification on an exercise intervention-induced improvements in body fatness and metabolic syndrome in obese women. Korean J. Obes. 2012, 21, 115–123. [Google Scholar] [CrossRef]
  25. Hoffman, M.A.; Driscoll, J.M. Health promotion and disease prevention: A concentric biopsychosocial model of health status. In Handbook of Counseling Psychology, 3rd ed.; Brown, S.D., Lent, R.W., Eds.; John Wiley & Sons, Inc: New York, NY, USA, 2000; pp. 532–567. [Google Scholar]
  26. Ra, J.S.; Kim, S.O. Beneficial effects of breastfeeding on the prevention of metabolic syndrome among postmenopausal women. Asian Nurs. Res. 2020, 14, 173–177. [Google Scholar] [CrossRef]
  27. Bener, A.; Darwish, S.; Al-Hamaq, A.O.; Yousafzai, M.T.; Nasralla, E.A. The potential impact of family history of metabolic syndrome and risk of type 2 diabetes mellitus: In a highly endogamous population. Indian J. Endocrinol. Metab. 2014, 18, 202–209. [Google Scholar] [CrossRef]
  28. Ranasinghe, P.; Cooray, D.N.; Jayawardena, R.; Katulanda, P. The influence of family history of hypertension on disease prevalence and associated metabolic risk factors among Sri Lankan adults. BMC Public Health 2015, 15, 576. [Google Scholar] [CrossRef] [Green Version]
  29. Tran, B.T.; Jeong, B.Y.; Oh, J.K. The prevalence trend of metabolic syndrome and its components and risk factors in Korean adults: Results from the Korean National Health and Nutrition Examination Survey 2008–2013. BMC Public Health 2017, 17, 71–78. [Google Scholar] [CrossRef] [Green Version]
  30. Bankoski, A.; Harris, T.B.; McClain, J.J.; Brychta, R.J.; Caserotti, P.; Chen, K.Y.; Koster, A. Sedentary activity associated with metabolic syndrome independent of physical activity. Diabetes Care 2011, 34, 497–503. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  31. Cho, K.I.; Kim, B.H.; Je, H.G.; Jang, J.S.; Park, Y.H. Gender-specific associations between socioeconomic status and psychological factors and metabolic syndrome in the Korean population: Findings from the 2013 Korean National Health and Nutrition Examination Survey. Biomed. Res Int. 2016, 2016, 3973197. [Google Scholar] [CrossRef]
  32. Park, Y.J.; Kim, H.S.; Kang, H.C. The age at menopause and related factors in Korean women. J. Korean Acad. Nurs. 2002, 32, 1024–1031. [Google Scholar] [CrossRef] [Green Version]
  33. Lee, S.; Park, H.S.; Kim, S.M.; Kwon, H.S.; Kim, D.Y.; Kim, D.J.; Yoo, H.J. Cut-off points of waist circumference for defining abdominal obesity in the Korean population. Korean J. Obes. 2006, 15, 1–9. [Google Scholar]
  34. UK Chief Medical Officers. UK Chief Medical Officers’ Physical Activity Guidelines. 2019. Available online: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attacment_data/file/832868/uk-chief-medical-officers-physical-activity-guidelines.pdf (accessed on 10 August 2020).
  35. World Health Organization. Global Physical Activity Questionnaire (GPAQ) Analysis Guide (Version 2.0). 2019. Available online: https://www.who.int/ncds/surveillance/steps/resources/GPAQ_Analysis_Guide.pdf (accessed on 10 August 2020).
  36. Kim, M.K.; Lee, W.-Y.; Kang, J.-H.; Kang, J.-H.; Kim, B.T.; Kim, S.M.; Kim, E.M.; Suh, S.-H.; Shin, H.J.; Lee, K.R.; et al. 2014 Clinical practice guidelines for overweight and obesity in Korea. Endocrinol. Metab. 2014, 29, 405–409. [Google Scholar] [CrossRef] [Green Version]
  37. Woo, S.M.; Jang, O.J.; Choi, H.K.; Lee, Y.R. Diagnostic availability and optimal cut off score of the Korea version of Alcohol Use Disorder Identification Test (AUDIT-K), Alcohol Consumption Questions (AUDIT-C) and Question 3 Alone (AUDIT3) for screening of hazardous drinking. J. Korean Acad. Addict. Psychiatry 2017, 21, 62–67. [Google Scholar] [CrossRef]
  38. Iftikhar, I.H.; Donley, M.A.; Mindel, J.; Pleister, A.; Soriano, S.; Magalang, U.J. Sleep duration and metabolic syndrome. An updated dose-risk metaanalysis. Ann. Am. Thorac. Soc. 2015, 12, 1364–1372. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Sowers, M.; Tisch, J. Insulin resistance, body weight, obesity, body composition, and the menopausal transition. In Menopause, Biology and Pathobiology; Lobo, R., Kelsey, J., Marcus, R., Eds.; Academic: San Diego, CA, USA, 2000; pp. 245–260. [Google Scholar]
  40. Geiselman, P.J.; Smith, S.R. Estrogen’s role in the regulation of appetite and body fat. In Scientific Evidence for Musculoskeletal, Bariatric, and Sports Nutrition; Kohlstadt, I., Ed.; CRC Press: Boca Raton, FL, USA, 2006; pp. 231–251. [Google Scholar]
  41. Rosique-Esteban, N.; Babio, N.; Díaz-López, A.; Romaquera, D.; Martínez, J.A.; Sanchez, V.M.; Salas-Salvadó, J. Leisure-time physical activity at moderate and high intensity is associated with parameters of body composition, muscle strength and sacopenia aged adults with obesity and metabolic syndrome from the PREDIMED-Plus study. Clin. Nutr. 2019, 38, 1324–1331. [Google Scholar] [CrossRef]
  42. Bowman, S.A. Television-viewing characteristics of adults: Correlations to eating practices and overweight and health status. Prev. Chronic Dis. 2006, 3, A38. [Google Scholar]
  43. Kikuchi, H.; Inoue, S.; Odagari, Y.; Inoue, M.; Swada, N.; Tsugane, S. Occupational sitting time and risk of all-cause mortality among Japanese workers. Scand. J. Work Environ. Health 2015, 41, 519–528. [Google Scholar] [CrossRef] [Green Version]
  44. Davies, K.A.B.; Sprung, V.S.; Norman, J.A.; Thompson, A.; Mitchell, K.L.; Harrold, J.A.; Finlayson, G.; Gibbons, C.; Wilding, J.; Kemp, G.; et al. Physical activity and sedentary time: Association with metabolic health and liver fat. Med. Sci. Sports Exerc. 2019, 51, 1169–1177. [Google Scholar] [CrossRef]
  45. Czaja, S.J.; Charness, N.; Fisk, A.D.; Hertzog, C.; Nair, S.N.; Rogers, W.A.; Sharit, J. Factors predicting the use of technology: Findings from the center for research and education on aging and technology enhancement (CREATE). Psychol. Aging 2006, 21, 333–352. [Google Scholar] [CrossRef] [Green Version]
  46. De Rezende, L.F.M.; Rey-López, J.P.; Matsudo, V.K.; do Carmo Luiz, O. Sedentary behavior and health outcomes among older adults: A systematic review. BMC Public Health 2014, 14, 333–341. [Google Scholar] [CrossRef] [Green Version]
  47. Smith, U.; Kahn, B.B. Adipose tissue regulates insulin sensitivity: Role of adipogenesis, de novo lipogenesis and novel lipids. J. Intern. Med. 2016, 280, 465–475. [Google Scholar] [CrossRef] [Green Version]
  48. Brown, M.D.; Korytkowski, M.T.; Zmuda, J.M.; McCole, S.D.; Moore, G.E.; Hagberg, J.M. Insulin sensitivity in postmenopausal women: Independent and combined associations with hormone replacement, cardiovascular fitness, and body composition. Diabetes Care 2000, 23, 1731–1736. [Google Scholar] [CrossRef] [Green Version]
  49. Kim, K.S.; Kim, S.J.; Kim, S.; Choi, D.W. Association of self-reported sedentary time with insulin resistance among Korean adults without diabetes mellitus: A cross-sectional study. BMC Public Health 2018, 18, 1335. [Google Scholar] [CrossRef]
  50. Van der Berg, J.D.; Stehouwer, C.D.A.; Bosma, H.; Van Der Velde, J.H.P.M.; Willems, P.J.B.; Savelberg, H.H.C.M.; Schram, M.; Sep, S.J.S.; Van Der Kallen, C.J.H.; Henry, R.M.A.; et al. Associations of total amount and patterns of sedentary behaviour with type 2 diabetes and the metabolic syndrome: The Maastricht study. Diabetologia 2016, 59, 709–718. [Google Scholar] [CrossRef]
  51. Hu, F.B.; Li, T.Y.; Colditz, G.A.; Willett, W.C.; Manson, J.E. Television watching and other sedentary behaviors in relation to risk of obesity and type 2 diabetes mellitus in women. JAMA 2003, 289, 1785–1791. [Google Scholar] [CrossRef] [Green Version]
  52. Dunstan, D.W.; Salmon, J.; Healy, G.N.; Shaw, J.E.; Jolley, D.; Zimmet, P.Z.; Owen, N. Association of television viewing with fasting and 2-h postchallenge plasma glucose levels in adults without diagnosed diabetes. Diabetes Care 2007, 30, 516–522. [Google Scholar] [CrossRef] [Green Version]
  53. Peddie, M.C.; Bone, J.L.; Rehrer, N.J.; Skeaff, C.M.; Gray, A.R.; Perry, T.L. Breaking prolonged sitting reduces post-prandial glycemia in healthy, normal-weight adults: A randomized crossover trial. Am. J. Clin. Nutr. 2013, 98, 358–366. [Google Scholar] [CrossRef] [Green Version]
  54. Yates, T.; Henson, J.; Edwardson, C.; Dunstan, D.; Bodicoat, D.H.; Khunti, K.; Davies, M.J. Objectively measured sedentary time and associations with insulin sensitivity: Importance of reallocating sedentary time to physical activity. Prev. Med. 2015, 76, 79–83. [Google Scholar] [CrossRef]
  55. Serrano-Sánchez, J.A.; Fernández-Rodríguez, M.J.; Sanchis-Moysi, J.; Rodríguez-Pérez, M.D.C.; Marcelino-Rodríguez, I.; Cabrera de León, A. Domain and intensity of physical activity are associated with metabolic syndrome: A population-based study. PLoS ONE 2019, 14, e0219798. [Google Scholar] [CrossRef] [Green Version]
  56. Johns, D.J.; Hartmann-Boyce, J.; Jebb, S.A.; Aveyard, P.; Group, B.W.M.R. Diet or exercise interventions vs combined behavioral weight management programs: A systematic review and meta-analysis of direct comparisons. J. Acad. Nutr. Diet. 2014, 114, 1557–1568. [Google Scholar] [CrossRef] [Green Version]
  57. Kim, J.H.; Cho, H.T.; Kim, Y.J. The role of estrogen in adipose tissue metabolism: Insights into glucose homeostasis regulation. Endocr. J. 2014, 1055–1067. [Google Scholar] [CrossRef] [Green Version]
Table
Table 1. Characteristics of Metabolic Syndrome, Unhealthy Lifestyle Behaviors, and Covariates among Participants (N = 6114).
Table 1. Characteristics of Metabolic Syndrome, Unhealthy Lifestyle Behaviors, and Covariates among Participants (N = 6114).
VariablesCategoriesn (%)
Metabolic syndrome Yes2939 (45.7)
No3175 (54.3)
Components of metabolic syndrome
Abdominal obesityYes2191 (34.0)
No3923 (66.0)
Elevated blood pressureYes3429 (52.6)
No2685 (47.4)
Low high density lipoprotein cholesterolYes3632 (57.4)
No2482 (42.6)
High triglyceridesYes2740 (43.3)
No3374 (56.7)
Impaired fasting glucose levelsYes2657 (42.7)
No3457 (57.3)
Unhealthy lifestyle behaviors
None 534 (9.2)
One unhealthy lifestyle behavior
Poor dietary behaviors 1561 (26.8)
Prolonged sedentary behaviors 468 (8.1)
Insufficient physical activity 281 (4.6)
Combining two unhealthy lifestyle behaviors
Poor dietary behaviors and prolonged sedentary behaviors 1105 (18.4)
Poor dietary behaviors and insufficient physical activity 901 (13.4)
Prolonged sedentary behaviors and insufficient physical activity 319 (5.0)
Combining three unhealthy lifestyle behaviors
Poor dietary behaviors, prolonged sedentary behaviors, and insufficient physical activity 945 (14.5)
Covariates
Biomedical factors
Age (years)40–643488 (63.3)
≥652626 (36.7)
Body mass indexUnderweight or normal weight2304 (39.7)
Overweight or obese3810 (60.3)
Family history of hypertension, type 2 diabetes mellitus, cerebro-cardiovascular disease, dyslipidemia Yes3993 (66.2)
No2121 (33.8)
Biosocial factors
Education levelLower than elementary school education2664 (38.1)
Graduation of middle school1071 (17.9)
Graduation of high school1559 (28.8)
College education or above820 (15.2)
Socioeconomic status of familyHigh1396 (26.1)
Middle2964 (48.8)
Low1754 (25.1)
Psychosocial factors
StressSevere1418 (23.8)
A little or not at all4696 (76.2)
DepressionYes519 (8.3)
No5595 (91.7)
Current or past smoking historyYes372 (6.4)
No5742 (93.6)
Current binge alcohol consumptionYes365 (7.1)
No5749 (92.9)
Sleep duration (hours)<72697 (45.7)
≥73417 (54.3)
Note: Values are presented as underweighted number (weighted percentage).
Table
Table 2. Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women (N = 6114).
Table 2. Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women (N = 6114).
Unhealthy Lifestyle Behaviors Metabolic SyndromeAbdominal ObesityElevated Blood PressureLow high Density Lipoprotein CholesterolHigh
Triglyceride		Impaired Fasting Glucose Levels
Adjusted odds ratio (95% Confidence Interval)
None (Reference) 1.001.001.001.001.001.00
One unhealthy lifestyle behaviorPoor dietary behaviors0.89 (0.67–1.18)1.23 (0.90–1.67)0.83 (0.65–1.06)0.87 (0.68–1.10)0.81 (0.63–1.04)1.10 (0.85–1.42)
Prolonged sedentary behaviors1.34 (0.95–1.87)1.59 (1.10–2.29) *0.94 (0.68–1.29)1.01 (0.75–1.36)1.02 (0.75–1.37)1.54 (1.13–2.10) *
Insufficient physical activity0.83 (0.57–1.22)1.08 (0.72–1.62)0.94 (0.63–1.39)0.73 (0.50–1.06)0.80 (0.57–1.12)1.04 (0.73–1.48)
Combining two unhealthy lifestyle behaviorsPoor dietary behaviors and prolonged sedentary behaviors1.00 (0.75–1.33)1.48 (1.10–2.00) *1.02 (0.79–1.31)1.08 (0.84–1.40)0.94 (0.73–1.21)1.49 (1.14–1.96) *
Poor dietary behaviors and insufficient physical activity1.11 (0.81–1.51)1.21 (0.89–1.64)1.03 (0.78–1.37)1.00 (0.76–1.31)0.92 (0.70–1.20)1.27 (0.95–1.69)
Prolonged sedentary behaviors and insufficient physical activity1.46 (0.99–2.14)2.81 (1.90–4.20) *1.2 9(0.90–1.84)1.01 (0.71–1.45)0.99 (0.70–1.41)1.59 (1.13–2.24) *
Combining all three unhealthy lifestyle behaviorsPoor dietary behaviors, prolonged sedentary behaviors, and insufficient physical activity1.24 (0.91–1.69)2.05 (1.50–2.80) *0.98 (0.74–1.30)1.22 (0.93–1.62)0.98 (0.75–1.30)1.71 (1.32–2.23) *
Note 1: Adjusted odds ratio = Adjusted for age, body mass index, family history, education level, economic status, stress, depression, smoking habits, binge alcohol consumption, and sleep duration. Note 2: * = p < 0.05. Note 3: Metabolic syndrome = presence of 3 or more of the following: (1) abdominal obesity (waist circumference ≥85 cm), (2) elevated blood pressure: ≥130/85 mmHg or on anti-hypertensive medications, (3) low HDL cholesterol: <50 mg/dL or on anti-dyslipidemic medications, (4) high triglyceride: ≥150 mg/dL or on anti-dyslipidemic medications, (5) impaired fasting glucose levels: ≥100 mg/dL or on anti-diabetic medications.
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Ra, J.-S.; Kim, H. Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women. Healthcare 2021, 9, 848. https://doi.org/10.3390/healthcare9070848

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Ra J-S, Kim H. Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women. Healthcare. 2021; 9(7):848. https://doi.org/10.3390/healthcare9070848

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Ra, Jin-Suk, and Hyesun Kim. 2021. "Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women" Healthcare 9, no. 7: 848. https://doi.org/10.3390/healthcare9070848

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Ra, J. -S., & Kim, H. (2021). Combined Effects of Unhealthy Lifestyle Behaviors on Metabolic Syndrome among Postmenopausal Women. Healthcare, 9(7), 848. https://doi.org/10.3390/healthcare9070848

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