Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Recommended Levels of Physical Activity Are Associated with Reduced Risk of the Metabolic Syndrome in Mexican-Americans

  • Shenghui Wu,

    Affiliation Department of Epidemiology & Biostatistics, University of Texas Health Science Center at San Antonio-Laredo Campus, Laredo, Texas, United States of America

  • Susan P. Fisher-Hoch,

    Affiliation Division of Epidemiology, University of Texas Health Science Center-Houston, School of Public Health, Brownsville Campus, Brownsville, Texas, United States of America

  • Belinda Reininger,

    Affiliation Division of Health Promotion and Health Behavior University of Texas Health Science Center-Houston, School of Public Health, Brownsville Campus, Brownsville, Texas, United States of America

  • Joseph B. McCormick

    Joseph.b.mccormick@uth.tmc.edu

    Affiliation Division of Epidemiology, University of Texas Health Science Center-Houston, School of Public Health, Brownsville Campus, Brownsville, Texas, United States of America

Abstract

Purpose

To measure the association between physical activity and the metabolic syndrome risk in Mexican-Americans.

Methods

Participants were drawn from the Cameron County Hispanic Cohort (n = 3,414), a randomly selected Mexican-American cohort in Texas on the US-Mexico border. Moderate and vigorous physical activity was assessed using reliable and validated instruments. The metabolic syndrome was defined as having 3 or more metabolic abnormalities.

Results

One thousand five hundred and twenty-four participants of the cohort (45.02%) were found to have the metabolic syndrome. Compared to participants who did not meet US physical activity guidelines, participants who met physical activity guidelines of 150 moderate and vigorous minutes per week (≥ 600 MET adjusted minutes) had 36% lower risk for the metabolic syndrome (OR = 0.64; 95% CI: 0.42–0.98), and participants with total minutes per week of moderate and vigorous/strenuous activity greater than 743 MET adjusted minutes had 37% lower risk for the metabolic syndrome (OR = 0.63; 95% CI: 0.42–0.94) compared with their counterparts, after adjusting for age, gender, annual household income, body mass index, smoking and alcohol drinking status, total portions of fruit and vegetable intake, census tracts and blocks, and survey version for physical activity.

Conclusions

Meeting or exceeding physical activity guidelines significantly was inversely associated with the risk for the metabolic syndrome in Mexican-Americans. Improving levels of physical activity appears to be an effective target for the metabolic syndrome prevention and control among Mexican-Americans independent of other factors.

Introduction

The metabolic syndrome is a major public health problem worldwide[1]. The metabolic syndrome is characterized by a clustering of risk factors, including obesity, hypertension, dyslipidemia, hyperglycemia, and hyperinsulinemia [2,3]. The National Health and Nutrition Examination Survey reported that using the National Cholesterol Education Program definition of the metabolic syndrome [2,3], the age-adjusted prevalence of the metabolic syndrome was 44.5% among Hispanic men, and 44.1% among Hispanic women [4]. It is now widely accepted that the metabolic syndrome has an important mediating role in the increased risk of cardiovascular disease and type 2 diabetes[2,3,5]. Prevention of the metabolic syndrome and treatment of its main characteristics are now considered of utmost importance in order to combat the epidemic of type 2 diabetes mellitus and to reduce the increased risk of cardiovascular disease and all-cause mortality[6]. As a modifiable lifestyle factor, the role of physical activity in health has been increasingly recognized [7]. However, the potential importance of physical activity in the development of the metabolic abnormalities has been less extensively investigated compared with other lifestyle changes and factors [6]. One meta-analysis pooling prospective cohort studies evaluated the association between physical activity and risk of the metabolic syndrome[8]. This meta-analysis of 17 cohort studies reported that a high level of leisure time physical activity was statistically associated with decreased risk of the metabolic syndrome [high vs. low: relative risk (RR) = 0.80, 95% confidence interval (CI) 0.75–0.85], whereas a moderate level of leisure time physical activity was weakly associated with decreased risk of the metabolic syndrome (moderate vs. low: RR = 0.95, 95% CI 0.91–1.00) [8]. However, compared with low level leisure time physical activity, Americans with high level leisure time physical activity did not significantly reduce the risk of the metabolic syndrome (all 95% CIs for each individual study across 1) based on four studies from the USA included into the meta-analysis [8]. Only one study conducted in Mexicans [9] reported the reduced risk of the metabolic syndrome from physical activity in Mexico, but not in Mexican-Americans in the US. The objective of this study was to explore the effect of physical activity on metabolic syndrome risk in a randomly selected cohort of Mexican-American subjects.

Materials and Methods

Study Participants

This study was approved by the Committee for the Protection of Human Subjects of the UT Health, Houston and the Institutional Review Board of the University of the Texas Health Science Center, San Antonio. All study participants gave written informed consent. This cross-sectional analysis used data from the Cameron County Hispanic Cohort (CCHC), an ongoing homogenous community-dwelling Mexican-American cohort study [10,11]. Study subjects were recruited from randomly selected tract/blocks according to the 2000 Census as described previously [10,11]. At the baseline survey conducted between 2003 and 2015, 3,414 participants aged 18 years or older were recruited from their households in three predominantly Mexican-American cities along the Rio Grande Border with Mexico. All participants recruited between 2003 and 2012 were from Brownsville, TX.

All subjects responded to a detailed baseline survey of demographic characteristics, lifestyle including diet, physical activity, family and medical history, and other exposures. Participants were asked to fast for at least 10 hours overnight before a clinic visit at the Clinical Research Unit. Anthropometric measurements, including current weight, height, and circumferences of the waist and hip, were also taken [10,11]. Physical activity in a typical week according to intensity, frequency (times / week) and duration (minutes / time) was assessed using the International Physical Activity Questionnaire short-form (IPAQ)[12] or the Godin Leisure-Time Exercise Questionnaire instruments [13] as reported previously [14]. The instruments have reported evidence of reliability and validity [12,1518]. Physical activity energy expenditure was estimated using standard metabolic equivalent (MET) values [19]. A MET is the ratio of the rate of energy expended during an activity to the rate of energy expended at rest. For example, 1 MET is the rate of energy expenditure while at rest. A 4 MET activity expends 4 times the energy used by the body at rest. If a person does a 4 MET activity for 30 minutes, he or she has done 4 × 30 = 120 MET-minutes (or 2.0 MET-hours) of physical activity [19]. Moderate-intensity activities are defined as 3.0 to 5.9 METs. Walking at 3.0 miles per hour requires 3.3 METs of energy expenditure and is therefore considered a moderate-intensity activity. Vigorous-intensity activities are defined as 6.0 METs or more. Running at 10 minutes per mile (6.0 mph) is a 10 MET activity and is therefore classified as vigorous intensity [19]. In this study, the MET adjusted minutes of moderate and vigorous physical activity in the last week was calculated based on responses [11]. Physical activity ≥ 600 MET adjusted minutes was considered meeting United States physical activity guidelines (USDHHS, 2008)[19].

All participants responded to a detailed baseline survey that collected information on demographic characteristics, lifestyle and dietary histories, medical history, and other exposures. Using the Food Frequency Questionnaire[20], fruit and vegetable consumption was assessed by asking participants how many portions of fruit and vegetables they ate daily. A portion size was described as a ½ cup of fresh, frozen, or canned produce or a medium-sized piece of produce (such as 130–189 berries per cup) [21,22]. Consumption of five or more fruit and vegetable portions was considered meeting US guidelines[21,22]. Weight was measured to the nearest tenth of a kilogram and height to the nearest tenth of a centimeter. Body mass index (BMI) was calculated as weight in kilograms divided by height squared in meters (kg/m2). Waist circumference (WC) was measured at the level of the umbilicus and hip circumference (HC) at the level of maximum width of the buttocks with participants in a standing position and breathing normally, to the nearest 0.2 cm. Waist-to-hip ratio (WHR) was calculated as WC divided by HC [10]. The average of 3 blood pressures (BP) taken 5 minutes apart were used.

Laboratory Measurements

All participants provided a blood sample at baseline. After collection, samples were placed on ice and centrifuged within 30 minutes of collection. Following processing and aliquoting, all samples were stored at -80°C until laboratory analyses were conducted. Laboratory studies performed included fasting lipid panel, hemoglobin (Hb) A1c and fasting plasma glucose was performed by a local CLIA certified laboratory. Fasting serum insulin was consistently performed in-house using Mercodia immunoassays (Uppsala, Sweden). Homeostasis model assessment insulin resistance index (HOMA-IR) was calculated as fasting glucose (mg/dL)/18 × fasting insulin (mU/L)/22.5 [23].

Definition of the metabolic syndrome

The metabolic syndrome was defined as having ≥ 3 of the following metabolic abnormalities: waist circumference (WC) ≥ 102 cm in men or ≥ 88 cm in women; systolic BP (SBP) ≥ 130 mmHg and/or diastolic BP (DBP) ≥ 85 mmHg or on antihypertensive medication; triglyceride ≥ 150 mg/dL; high-density lipoprotein cholesterol < 40 mg/dL in men or < 50 mg/dL in women; fasting glucose ≥ 100 mg/dL or on diabetes medication [2,3].

Statistical analysis

Descriptive results and the models reported in this paper were adjusted for the probability sampling weights also taking into consideration clustering effects arising from the census block and household [10]. Log-transformation was conducted to normalize the distribution of continuous variables as appropriate. Survey-weighted linear regression was used to obtain the t-test statistics to compare phenotypes and to be used for multiple pairwise mean comparisons for continuous data. Survey-weighted chi-square test was used to obtain Rao-Scott F adjusted chi-square statistic to compare phenotypes for categorical data. Survey-weighted logistic regression modeling was performed to estimate the ORs for metabolic syndrome risk and their 95% CIs by physical activity adjusting for other covariates. Potential confounders adjusted for in multivariable survey-weighted logistic regression models included age, gender, annual household income, BMI, alcohol drinking, cigarette smoking status, and discrepancies in survey versions for physical activity data collection. Physical activity was classified into two groups respectively according to the mean of the total minutes per week of moderate and vigorous/strenuous activity (743 MET adjusted minutes), and if participants met physical activity guidelines of 150 moderate and vigorous minutes per week (≥ 600 MET adjusted minutes). The unit of physical activity was changed from minutes to hours when it was continuous variable so as to avoid too small ORs.

To illustrate the dose-response relationship between physical activity and the metabolic syndrome, we also used a restricted cubic spline logistic regression analysis[24] to evaluate the risk of the metabolic syndrome with total MET adjusted hours per week of moderate and vigorous/strenuous activity. Knots were placed at the 5th, 50th, and 95th percentiles of the distribution of age at enrollment.

Statistical analyses were carried out by using SAS version 9.3 (SAS Institute, Cary, NC). All statistical tests were based on 2-sided probability.

Results

At the time of this study a total of 3,414 individuals were enrolled in the CCHC, 2,944 from Brownsville, 272 participants from Harlingen and 198 participants from Laredo, Texas. Based on the recommended scoring protocols, 29 (0.8%) participants with extreme values (≥ 7,680 MET adjusted minutes) of physical activity were excluded from the analyses. Of the remaining 3,385 participants, mean age of this subset was 45 years; 34% were male. A total of 12.6% (n = 427) of the participants met minimum recommendations for physical activity of ≥ 600 MET adjusted minutes per week.

One thousand five hundred and twenty-four participants of the cohort (45.02%) were found to have the metabolic syndrome and 1,861 did not report the metabolic syndrome (Table 1). Participants with the metabolic syndrome were more likely to be older, and less likely to meet the recommended guidelines for physical activity of more than 600 MET adjusted minutes per week or meet the recommended guidelines for fruit and vegetables more than 5 servings per day. They had lower all physical activity, moderate and vigorous activity and average daily time doing heavy activity, but higher BMI, WC, WHR, systolic and diastolic blood pressure, insulin, fasting blood glucose, HOMA-IR and HbA1c than their counterparts (all Ps < 0.05). They showed significantly elevated mean values of triglycerides compared with subjects without the metabolic syndrome, but decreased values of high density lipid cholesterol (HDLC). Although levels of total cholesterol were higher and consumption of total portions of fruit and vegetables were lower in subjects with the metabolic syndrome than those without, the differences were not statistically significant. There was no difference in gender, annual household income, employed status, education level, current and ever cigarette smoking status, ever alcohol drinking, time spent in doing mild physical activity, and mean levels of low-density lipoprotein between subjects with and without the metabolic syndrome.

thumbnail
Table 1. Cohort Demographics and Metabolic Characteristics Stratified by Metabolic syndrome Risk: Cameron County Hispanic Cohort Study (2003–2015)a,b.

https://doi.org/10.1371/journal.pone.0152896.t001

Participants who met physical activity guidelines of 150 moderate and vigorous minutes per week (≥ 600 MET adjusted minutes) had 31% lower risk for the metabolic syndrome (OR = 0.69; 95% CI: 0.54–0.88) after adjusting for age and gender compared with those who did not meet guidelines (Table 2). Multivariable-adjusted model showed that meeting physical activity guidelines was associated with 36% lower total risk for the metabolic syndrome (OR = 0.64; 95% CI: 0.42–0.98) after further adjusting for annual household income, smoking, alcohol drinking, BMI, total consumption of fruit and vegetables, census tracts and blocks, and discrepancies in survey versions for physical activity data collection. Compared to participants with total minutes per week of moderate and vigorous/strenuous activity less than 743 MET adjusted minutes, participants with those greater than 743 MET adjusted minutes had 33% (OR = 0.67; 95% CI: 0.52–0.86) lower risk of the metabolic syndrome after adjusting for age and gender (Table 2). Multivariable-adjusted model showed that participants with those greater than 743 MET adjusted minutes had 37% lower risk (OR = 0.63; 95% CI: 0.42–0.94).

thumbnail
Table 2. Association between physical activity and risk for the metabolic syndrome.

https://doi.org/10.1371/journal.pone.0152896.t002

Fig 1 visually depicts the shape of the dose-response relationship between physical activity and the metabolic syndrome risk after adjusting for potential confounding variables in a restricted cubic spline model. Total metabolic equivalent hours of physical activity per week was inversely associated with the risk for the metabolic syndrome (P for overall association = 0.02). The linear trend was not statistically significant (P = 0.12). Although ORs less than 30 MET hours/week were not statistically significant (95% CIs across 1) in Fig 1, the findings were not conflicted with Table 2 due to the different purposes and meanings of ORs in Fig 1 and Table 2. ORs in Table 2 were comparisons between participants with MET adjusted minutes ≥ 600 and those with MET adjusted minutes < 600 or between participants with MET adjusted minutes ≥ 743 and those with MET adjusted minutes < 743. ORs in Fig 1 were the odds ratios of the metabolic syndrome corresponding to MET adjusted hours per week in moderate and vigorous activity.

thumbnail
Fig 1. Smoothed plot for odds ratios (ORs) of the metabolic syndrome risk according to total metabolic equivalent (MET) hours of physical activity per week.

The ORs were estimated by using the restricted cubic-spline logistic regression models with knots placed at the 5th, 50th, and 95th percentiles of physical activity. The overall association between physical activity and the risk of the metabolic syndrome was significant (P = 0.02). The model was adjusted for age, sex, annual household income, cigarette smoking status, alcohol drinking status, body mass index, total consumption of fruit and vegetables, discrepancies in survey versions for physical activity data collection and the probability of sampling using weights taking into consideration clustering effects arising from the same census block and household.

https://doi.org/10.1371/journal.pone.0152896.g001

Discussion

In a Mexican-American cohort, participants who met physical activity guidelines of 150 moderate and vigorous minutes per week (≥ 600 MET adjusted minutes) had significantly 36% lower for the metabolic syndrome risk, and participants with total minutes per week of moderate and vigorous/strenuous activity greater than 743 MET adjusted minutes had significantly 37% lower for the metabolic syndrome risk, compared with their corresponding counterparts, after adjusting for covariates. Cubic spline logistic regression showed the dose-response relationship that total metabolic equivalent hours of moderate and vigorous physical activity per week was inversely associated with the risk for the metabolic syndrome.

To our knowledge, this study is the first to examine the inverse association between moderate and vigorous physical activity and the risk for the metabolic syndrome among Mexican-Americans. According to the United States physical activity guidelines (USDHHS, 2008)[19], moderate vigorous physical activities in this study include walking briskly (3 miles per hour or faster, but not race-walking), water aerobics, bicycling slower than 10 miles per hour, tennis (doubles), ballroom dancing and general gardening; vigorous physical activities include race walking, jogging, or running, swimming laps, tennis (singles), aerobic dancing, bicycling 10 miles per hour or faster, jumping rope, heavy gardening (continuous digging or hoeing, with heart rate increases) and hiking uphill or with a heavy backpack. Prior cross-sectional studies found an inverse gradient between amount of physical activity and the metabolic syndrome in participants with mixed ethnicities adjusting for ethnicity and other covariates [25,26]. One meta-analyses of prospective cohort studies conducted in people from Europe, America, Asia and South America reported that a high level of leisure time physical activity was statistically associated with decreased risk of the metabolic syndrome[8], however, a moderate level of leisure time physical activity was non-significantly associated with decreased risk of the metabolic syndrome [8], and Americans with high level leisure time physical activity did not statistically significantly reduce the risk of the metabolic syndrome based on the four studies from USA included into the meta-analysis [8]. Only one study conducted in Mexico [9] showed that the metabolic syndrome risk was reduced among men (OR = 0.72; 95% CI = 0.57–0.95) and women (OR = 0.78; 95% CI = 0.64–0.94) who reported an amount of ≥ 30 minutes/day of leisure time activity, and among women who reported an amount of ≥ 3 hours/day of workplace activity (OR = 0.75; 95% CI = 0.59–0.96)[9]. This study further provided evidence showing the beneficial effect of physical activity on the risk for the metabolic syndrome in Mexican-Americans. Compared to participants who did not meet US physical activity guidelines, participants who met physical activity guidelines of 150 moderate and vigorous minutes per week (≥ 600 MET adjusted minutes) had 36% lower risk for the metabolic syndrome. This study is also the first to report the inverse dose-response relationship between moderate and vigorous physical activity and the risk for the metabolic syndrome. We found the dose-response relationship is also shown in the cubic spline regression (Fig 1). This study suggested that even 1 hour moderate and vigorous physical activity per week is helpful to lower the risk of the metabolic syndrome. Although further longitudinal data is needed, our findings still provide important information for the prevention and control of the metabolic syndrome and related conditions among Mexican-Americans.

Potential mechanisms influenced by exercise involved in the components of the metabolic syndrome may include alterations in abdominal adipose tissue accumulation[27], glucose [27,28], dyslipidaemia[6] and blood pressure [29]. Genetic predisposition (related to several candidate genes[30]) in combination with the effect of environmental factors is likely to influence the development of insulin resistance and/or the clinical expression of the metabolic syndrome[6]. Consistently, we found that participants with physical activity levels < 743 MET adjusted minutes had higher levels of WC (106.4 vs. 101.4; P = 0.01), systolic blood pressure (125.4 vs 118.2 mmHg; P = 0.01), diastolic blood pressure (76.2 vs 74.8 mmHg; P = 0.20), fasting blood glucose (113.6 vs. 97.1 mg/dL; P < 0.0001) and triglyceride (161.2 vs. 136.5 mg/dL; P = 0.01), but lower levels of HDLC (45.59 vs 50.74 mg/dL; P = 0.048), compared to participants with physical activity levels ≥ 743 MET adjusted minutes.

There are some methodological limitations in our research. The study was cross-sectional in design; thus, only associations but not causal relationship may be inferred. Prospective studies are needed to further investigate the effect or dose-response of physical activity on metabolic syndrome risk. Our longitudinal data currently being collected will provide that opportunity. Physical activity was self-reported, which may affect its precision as a predictor. We could not completely rule out the possibility of residual confounding due to unmeasured or inadequately measured covariates.

This study had several strengths. First, this is a general population-based randomly selected Mexican-American cohort with relatively large sample size, thus avoiding bias inherent in studies drawing from clinic populations or other non-randomly selected populations with established disease or mixed ethnicity. Second, we first found an inverse dose-response relationship between physical activity and the metabolic syndrome in Mexican-Americans. Finally, detailed assessment of physical activity and information on a wide range of factors related to the metabolic syndrome was available, allowing us to get a relatively comprehensive analysis of the relevant factors. If having the metabolic syndrome might have increased physical activity as a result we did not observe this in our robust baseline cohort population.

Conclusion

Increased moderate and vigorous physical activity was associated with a significant risk for the metabolic syndrome after excluding the effect of other confounding factors. Therefore, physical activity might be a modifiable protective factor for which Mexican-Americans can make changes to reduce their metabolic syndrome risk. Efforts need to be focused on improving physical activity intervention.

Acknowledgments

We thank our cohort team, particularly, Rocio Uribe (Brownsville), Becky Erazo (Laredo), Ariana Garza (Harlingen) and their teams, who recruited and documented the participants. We also thank Marcela Morris and other laboratory staff for their contributions, and Christina Villarreal for administrative support. We thank Valley Baptist Medical Center, Brownsville, Texas for providing us space for our Center for Clinical and Translational Science Clinical Research Unit. We also thank the community of Brownsville, Laredo and Harlingen and the participants who so willingly participated in this study in their city.

Author Contributions

Conceived and designed the experiments: JBM SFH. Performed the experiments: JBM SFH BR SW. Analyzed the data: SW. Contributed reagents/materials/analysis tools: JBM SFH BR SW. Wrote the paper: SW JBM SFH BR.

References

  1. 1. Zimmet P, Magliano D, Matsuzawa Y, Alberti G, Shaw J. The metabolic syndrome: a global public health problem and a new definition. J Atheroscler Thromb. 2005;12: 295–300. JST.JSTAGE/jat/12.295 [pii]. pmid:16394610
  2. 2. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112: 2735–2752. [pii]; pmid:16157765
  3. 3. Wildman RP, Muntner P, Reynolds K, McGinn AP, Rajpathak S, Wylie-Rosett J, et al. The obese without cardiometabolic risk factor clustering and the normal weight with cardiometabolic risk factor clustering: prevalence and correlates of 2 phenotypes among the US population (NHANES 1999–2004). Arch Intern Med. 2008;168: 1617–1624. [pii]; pmid:18695075
  4. 4. Ford ES, Li C, Zhao G. Prevalence and correlates of metabolic syndrome based on a harmonious definition among adults in the US. J Diabetes. 2010;2: 180–193. pmid:20923483
  5. 5. Meigs JB. Epidemiology of the metabolic syndrome, 2002. Am J Manag Care. 2002;8: S283–S292. [pii]. pmid:12240700
  6. 6. Carroll S, Dudfield M. What is the relationship between exercise and metabolic abnormalities? A review of the metabolic syndrome. Sports Med. 2004;34: 371–418. [pii]. pmid:15157122
  7. 7. World Health Organization (WHO). Global Recommendations on Physical Activity for Health. 2010.
  8. 8. He D, Xi B, Xue J, Huai P, Zhang M, Li J. Association between leisure time physical activity and metabolic syndrome: a meta-analysis of prospective cohort studies. Endocrine. 2014;46: 231–240. pmid:24287790
  9. 9. Mendez-Hernandez P, Flores Y, Siani C, Lamure M, Dosamantes-Carrasco LD, Halley-Castillo E, et al. Physical activity and risk of metabolic syndrome in an urban Mexican cohort. BMC Public Health. 2009;9: 276. [pii]; pmid:19646257
  10. 10. Fisher-Hoch SP, Rentfro AR, Salinas JJ, Perez A, Brown HS, Reininger BM, et al. Socioeconomic status and prevalence of obesity and diabetes in a Mexican American community, Cameron County, Texas, 2004–2007. Prev Chronic Dis. 2010;7: A53. [pii]. pmid:20394692
  11. 11. Fisher-Hoch SP, Vatcheva KP, Laing ST, Hossain MM, Rahbar MH, Hanis CL, et al. Missed opportunities for diagnosis and treatment of diabetes, hypertension, and hypercholesterolemia in a Mexican American population, Cameron County Hispanic Cohort, 2003–2008. Prev Chronic Dis. 2012;9: 110298. [pii]. pmid:22863308
  12. 12. Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, et al. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc. 2003;35: 1381–1395. pmid:12900694
  13. 13. Gofin G, Shephard RJ. Godin leisure-time exercise questionnaire. Med Sci Sports Exerc. 2015;29: S36–S38.
  14. 14. Reininger BM, Mitchell-Bennett L, Lee M, Gowen RZ, Barroso CS, Gay JL, et al. Tu Salud, inverted exclamation markSi Cuenta!: Exposure to a community-wide campaign and its associations with physical activity and fruit and vegetable consumption among individuals of Mexican descent. Soc Sci Med. 2015;143: 98–106.S0277-9536(15)30081-2 [pii]; pmid:26347959
  15. 15. Bauman A, Bull F, Chey T, Craig CL, Ainsworth BE, Sallis JF, et al. The International Prevalence Study on Physical Activity: results from 20 countries. Int J Behav Nutr Phys Act. 2009;6: 21. [pii]; pmid:19335883
  16. 16. Hallal PC, Gomez LF, Parra DC, Lobelo F, Mosquera J, Florindo AA, et al. Lessons learned after 10 years of IPAQ use in Brazil and Colombia. J Phys Act Health. 2010;7 Suppl 2: S259–S264. pmid:20702914
  17. 17. Rauh MJ, Hovell MF, Hofstetter CR, Sallis JF, Gleghorn A. Reliability and validity of self-reported physical activity in Latinos. Int J Epidemiol. 1992;21: 966–971. pmid:1468861
  18. 18. Dang, MM. Evidence of Reliability and Validity of IPAQ for Mexican-american Adults (Order No. 1470212). Dissertation. Dissertations & Theses @ University of Texas Health Science Center at Houston.2009. Available: http://search.proquest.com/docview/305004711.
  19. 19. USDHHS. 2008 Physical activity guidelines for Americans. 2008.
  20. 20. Reininger BM, Wang J, Fisher-Hoch SP, Boutte A, Vatcheva K, McCormick JB. Non-communicable diseases and preventive health behaviors: a comparison of Hispanics nationally and those living along the US-Mexico border. BMC Public Health. 2015;15: 564. [pii]. pmid:26088129
  21. 21. US Department of Agriculture. Choose My Plate, Food Groups. 2013.
  22. 22. US Department of Agriculture. Choose My Plate, Vegetables. 2013.
  23. 23. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28: 412–419. pmid:3899825
  24. 24. Harrell FJ Jr. (2001) Regression modeling strategies: with applications to linear models, logistic regression, survival analysis. New York, NY: Springer-Verlag.
  25. 25. Ford ES, Kohl HW III, Mokdad AH, Ajani UA. Sedentary behavior, physical activity, and the metabolic syndrome among U.S. adults. Obes Res. 2005;13: 608–614. [pii]; pmid:15833947
  26. 26. Zhu S, St-Onge MP, Heshka S, Heymsfield SB. Lifestyle behaviors associated with lower risk of having the metabolic syndrome. Metabolism. 2004;53: 1503–1511.S0026049504002136 [pii]. pmid:15536610
  27. 27. Ross R, Dagnone D, Jones PJ, Smith H, Paddags A, Hudson R, et al. Reduction in obesity and related comorbid conditions after diet-induced weight loss or exercise-induced weight loss in men. A randomized, controlled trial. Ann Intern Med. 2000;133: 92–103.200007180–00008 [pii]. pmid:10896648
  28. 28. Torjesen PA, Birkeland KI, Anderssen SA, Hjermann I, Holme I, Urdal P. Lifestyle changes may reverse development of the insulin resistance syndrome. The Oslo Diet and Exercise Study: a randomized trial. Diabetes Care. 1997;20: 26–31. pmid:9028689
  29. 29. Hagberg JM, Park JJ, Brown MD. The role of exercise training in the treatment of hypertension: an update. Sports Med. 2000;30: 193–206. pmid:10999423
  30. 30. Groop L. Genetics of the metabolic syndrome. Br J Nutr. 2000;83 Suppl 1: S39–S48.S0007114500000945 [pii]. pmid:10889791