The Association between Metabolic Syndrome and Related Factors among the Community-Dwelling Indigenous Population in Taiwan
by
, and
Yu-Chung Tsao
1,2
,
Wen-Cheng Li
2,3,4,
Wei-Chung Yeh
3,
Steve Wen-Neng Ueng
2,5,*,
Sherry Yueh-Hsia Chiu
6,7 and
Jau-Yuan Chen
2,3,* 1
Department of Occupational Medicine, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan City 33305, Taiwan
2
College of Medicine, Chang Gung University, Taoyuan City 33302, Taiwan
3
Department of Family Medicine, Chang-Gung Memorial Hospital, Linkou Branch, Taoyuan City 33305, Taiwan
4
Department of Health Management, Xiamen Chang-Gung Hospital, Xiamen 361028, China
5
Department of Orthopedics, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan City 33305, Taiwan
6
Department of Health Care Management, College of Management, Chang Gung University, Taoyuan City 33302, Taiwan
7
Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung Branch 83301, Taiwan
*
Authors to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2020, 17(23), 8958; https://doi.org/10.3390/ijerph17238958
Submission received: 20 October 2020
/
Revised: 26 November 2020
/
Accepted: 28 November 2020
/
Published: 2 December 2020
(This article belongs to the Special Issue Towards a Public Health Wellness: Psychosocial & Physical Health in Community)
Abstract
:The aim of this study was to conduct a community-based study with a view to construct a detailed analysis about metabolic syndrome and the related risk factors of the indigenous population. This was an observational, population-based and cross-sectional study that was conducted in remote villages of an indigenous community in northern Taiwan between 2010 and 2013. A total of 586 participants, 275 men and 311 women, were eligible for analysis. The participants underwent a questionnaire survey that included demographic and health behavior issues. An anthropometric assessment and measurements of blood pressure were carried out including serum biochemical variables. Metabolic syndrome (MetS) was defined by following the criteria provided by the modified Adult Treatment Panel III (ATP III) criteria of the National Cholesterol Education Program (NCEP). Univariate and multiple logistic regressions were used to identify the risk factors for metabolic syndrome. The standardized prevalence rates of substance use (cigarette smoking, alcohol drinking and betel nut chewing) were significantly higher than the general population regardless of whether it was northern, central or southern Taiwan and this was especially the case with betel nut chewing in women. The prevalence rate of metabolic syndrome was 42.9% in the indigenous population with 41.3% in men and 44.4% in women, which was higher than for urban Taiwanese. In the multiple logistic regression models, we found that the significant associated factors for metabolic syndrome were older age, lower education level, high levels of uric acid, alanine transaminase (ALT), gamma-glutamyl transferase (γ-GT) and creatinine. A higher prevalence rate of metabolic syndrome and substance use were observed in the indigenous population compared with urban Taiwanese, especially in women.
1. Introduction
Metabolic syndrome is a complex of interrelated risk factors for cardiovascular disease (CVD) and diabetes (DM). These factors include dysglycemia, raised blood pressure, elevated triglyceride levels, low high-density lipoprotein cholesterol levels and obesity (particularly central adiposity) [1,2]. Individuals with metabolic syndrome are associated with approximately five and two-fold increased risk for type 2 DM and CVD, respectively [3], as well as a risk factor for all-cause mortality [4]. Recent interest has focused on the possible involvement of insulin resistance as a linking factor although the pathogenesis remains unclear. With these risk factors, it has been demonstrated clearly that the syndrome is common and that it has a rising prevalence worldwide, which relates largely to increasing obesity and sedentary lifestyles. As a result, metabolic syndrome is now both a public health and a clinical problem. In the public health arena, more attention must be given to modification of lifestyles of the general public of all nations to reduce obesity and to increase physical activity. At a clinical level, individual patients with metabolic syndrome need to be identified so that their multiple risk factors, including lifestyle risk factors, can be reduced [1].
The prevalence of metabolic syndrome in Taiwan had been well described in recent studies [5,6]. The comparison between Taiwan and other Asian countries was also described [7]. In other countries, a higher prevalence among the indigenous population is one of the greatly emphasized public health issues [8]. However, there have been only scanty studies with small sample sizes [9,10] or a few hospital-based studies [11] that focused on the health issue of metabolic syndrome of the indigenous population in Taiwan. We aimed to conduct a community-based study with a view to constructing a detailed analysis about metabolic syndrome and related factors among an indigenous population in Taiwan. Therefore, our findings hopefully may provide valuable information for the prevention of metabolic syndrome (MetS) by further health promoting programs or intervention in this population.
2. Materials and Methods
2.1. Participants
We conducted a cross-sectional study with a design based on the annual health checkup service to collect associated information between October 2010 and February 2013 from three remote villages in the Fuxing District, Taoyuan City, Taiwan (as shown in Figure 1). Participants were informed about this study and voluntarily agreed to participate. The study was approved by the Chang Gung Medical Foundation 74 Institutional Review Board (99-0231B, 101-4156A3). Participants were recruited if they were over the age of 18 and had lived in this area for more than six months. A total of 2309 residents met our inclusion criteria.
We distributed questionnaires that included basic information about personal history, occupation, substance use and exercise habits. We also arranged free health checks that included basic laboratory data. According to the data from Fuxing District Health Station, the number of actual residents who lived in the three remote villages was around 1850. Therefore, after the exclusion of potential participants with incomplete data, we had a coverage rate of 42.1% over laboratory data (n = 778) and 50.7% over complete questionnaires (n = 938). With a view to evaluating the prevalence of metabolic syndrome and related factors, we excluded those who could not be identified with the criteria of metabolic syndrome due to missing data. With these exclusion criteria, we had a coverage rate of 31.7% (n = 586).
Figure 1 outlines the geographic location of the mountainous area (Fuxing District) in Taoyuan city. Gaoyi, Hualing and Sanguang were the three indigenous villages where we performed the integrated delivery system. Local medical care resources and local churches were marked on the map.
2.2. Questionnaire
A questionnaire was used to obtain socio-demographic data (i.e., race, gender, age, education level, religion, marital status, occupation and income) as well as information on tobacco, alcohol, betel quid usage and physical activity status. Smoking, drinking and betel nut usage were categorized as either current, never or past user. Smoking and betel nut usage were defined as at least three days a week in the recent month. An alcohol drinking habit was defined as more than three times a week.
Definitions of Metabolic Syndrome and Measurements
Metabolic syndrome was defined by following the criteria provided by the modified Adult Treatment Panel III (ATP III) criteria of the National Cholesterol Education Program (NCEP) [3]. The presence of any three of the following five factors was required for a diagnosis of metabolic syndrome: abdominal obesity (90 cm for Asian men and 80 cm for Asian women), hypertriglyceridemia (triglycerides ≥ 150 mg/dl or current use of triglycerides-lowering drugs), low high-density lipoprotein cholesterol (HDL) (HDL cholesterol < 40 mg/dL for men and <50 mg/dL for women), elevated blood pressure (systolic blood pressure ≥ 130 mmHg and/or diastolic blood pressure ≥ 85 mmHg or current use of anti-hypertensive drugs) and impaired fasting glucose (fasting plasma glucose ≥ 100 mg/dL or current use of anti-diabetic drugs).
Blood samples were drawn from the antecubital vein following a 12-h overnight fast. After centrifugation at standard conditions, plasma samples were frozen and transported immediately to our laboratory where they were analyzed. Participants’ medical history on using anti-hypertensive and anti-diabetic medication and participants with high blood pressure or DM were recorded.
The waist circumference was measured midway between the iliac and costal margin whilst the participant was standing. The procedure used for blood pressure measurements was in agreement with the recommendations of the American Society of Hypertension, where all blood pressure measurements were conducted on the upper arm of the subject with an automatic blood pressure recorder after a 5 min resting period.
All blood analyses were performed at the clinical laboratory department of the Linkou Chang Gung Memorial Hospital and certified by the College of American Pathologists (CAP). Biochemical parameters, including high-density lipoprotein cholesterol (HDL-C), triglycerides, fasting glucose, alanine transaminase (ALT gamma-glutamyl transferase), aspartate transaminase (AST), gamma-glutamyl transferase (γ-GT), high sensitive C-reactive protein (HS-CRP), glycohemoglobulin (HbA1c), uric acid, urinary microalbumin, creatinine, low-density lipoprotein cholesterol (LDL-C) and very-low-density lipoprotein cholesterol (VLDL-C) were analyzed on a Hitachi 7600–210 autoanalyzer (Hitachi, Tokyo, Japan). Blood tests were carried out in accordance with the hospital’s laboratory standard operating procedure that was accredited by the CAP. The aforementioned biomarkers related to metabolic syndrome were selected according to previous studies [12].
2.3. Statistical Analysis
Descriptive statistics for demographic and biochemical variables were computed separately for male and female genders. The differences between the two groups were analyzed by t-tests or Mann–Whitney U tests of independent samples. We performed a standardized method using the WHO 2000 population [13] for prevalence comparison. The univariate and multiple logistic regressions were used for risk factor investigations. All statistical analyses were performed using SAS software version 9.4 (SAS Institute Inc., Cary, NC, USA). All tests were two tailed and a p-value of <0.05 was considered statistically significant.
3. Results
3.1. Metabolic Syndrome
3.2. Substance Use
The overall crude prevalence rate of smoking was 26.4%, with 36.8% in males and 18.1% in females. The prevalence rate of alcohol drinking was 33.3%, with males 38.0% and females 29.6%. The prevalence rate of betel quid chewing was 14.1%, with males 21.3% and females 8.3%. The standardized prevalence rate of smoking, alcohol drinking and betel quid chewing were 33.3% (male 45.3%, female 25.9%), 36.7% (male 39.1%, female 35.0%) and 18.0% (male 31.9%, female 10.0%), respectively (Table 2). We chose three urban areas in Taiwan for comparison and found that the prevalence rates of substance usage were higher than in the urban area especially in alcohol drinking and betel nut chewing. The relatively higher prevalence rates of substance usage among the indigenous female population were also observed, with 25.9% smoking (9.4%, 2.5% and 2.7% in urban areas), 35.0% alcohol drinking (9.4%, 1.7% and 1.7% in urban areas) and 10.0% betel nut chewing (7.2%, 6.5% and 5.4% in urban areas) [14,15].
3.3. Regression Models
We built single and multiple regression models (Table 3) to discuss the related factors that are associated with metabolic syndrome. The crude odds ratio (OR) and adjusted OR are listed in Table 3. The crude ORs that were significant for metabolic syndrome were 1.03 (95% CI: 1.02, 1.04) in older age; 0.47 (95% CI: 0.31, 0.73) and 0.44 (95% CI: 0.22, 0.88) in better income; 0.48 (95% CI: 0.30, 0.76), 0.32 (95% CI: 0.19, 0.54) and 0.33 (95% CI: 0.14, 0.79) in better education; 1.93 (95% CI: 1.24, 3.02) in abnormal uric acid; 1.85 (95% CI: 1.21, 2.83) in abnormal ALT and 6.55 (95% CI: 1.86, 23.06) in abnormal creatinine. After adjusting for age and sex, the odds ratios that were significant for metabolic syndrome were 0.60 (95% CI: 0.38, 0.94) in better income, 0.46 (95% CI: 0.26, 0.83) in better education, 2.21 (95% CI: 1.22, 4.00) in betel nut chewing, 2.31 (95% CI: 1.43, 3.74) in abnormal uric acid, 1.68 (95% CI: 1.09, 2.61) in abnormal AST, 2.32 (95% CI: 1.65, 3.97) in abnormal ALT, 2.56 (95% CI: 1.65, 3.97) in abnormal γ-GT and 4.82 (95% CI: 1.33, 17.40) in abnormal creatinine. We built multiple logistic regression models and found that the models showed ORs that were significant for metabolic syndrome were 1.03 (95% CI: 1.01, 1.04) in older age, 0.44 (95% CI: 0.24, 0.83) in better education, 2.06 (95% CI: 1.22, 3.48) in abnormal uric acid, 2.02 (95% CI: 1.24, 3.29) in abnormal ALT, 1.86 (95% CI: 1.13, 3.07) in abnormal γ-GT and 5.38 (95% CI: 1.25, 23.10) in abnormal creatinine.
4. Discussion
4.1. Metabolic Syndrome
The prevalence rate of metabolic syndrome was 42.9% in the indigenous group we observed, with 41.3% in males and 44.4% in females. We performed a standardized method using the WHO 2000 population for prevalence comparison and the standardized prevalence rate of metabolic syndrome was 30.0%, with 31.9% in males and 28.3% in females. The prevalence rate was higher than that of urban Taiwanese based on recent studies with 28.6% in males and 18.8% in females [5], or similar with that of 32.4% in males and 27.8% in females [6].
A previous cross-sectional study conducted in 2008 focusing on an indigenous population (n = 725) in middle Taiwan showed that the prevalence rate of metabolic syndrome was 42.6%, with 41.5% in males and 43.5% in females [10]. This study showed a similar prevalence rate of metabolic syndrome with our study. Another study conducted in 2007 found that the prevalence rate of metabolic syndrome in aborigines (n = 90) in southern Taiwan was 83.3% (64.0% in males, 90.8% in females), which was higher than urban Taiwanese (46.6% and 40.6%, respectively) [9]. Another hospital-based study conducted in 2008 found that the prevalence rate of metabolic syndrome among indigenous people (n = 1226) in southeastern Taiwan was 58.7% (50.3% in males, 68.5% in females) [11].
Studies focusing on the indigenous population in other countries also showed the trend of higher prevalence rates of metabolic syndrome compared with other ethnic groups. The prevalence rate ranged from 21.4% to 37.2% in a Canadian study [8]. They suggested that the results in the indigenous community indicated that MetS was inversely associated with physical activity and fitness.
4.2. Substance Use
The prevalence rates for substance usage investigated by the Health Promotion Administration of Taiwan was 18.7% for smoking in 2012 and 7.8% for betel nut chewing in 2009. The prevalence rates of alcohol drinking habits among urban Taiwanese ranged from 5.6% to 8.3% [16,17,18]. The standardized prevalence rate of smoking, alcohol drinking and betel nut chewing in the indigenous group we addressed were 33.3% (male 45.3%, female 25.9%), 36.7% (male 39.1%, female 35.0%) and 18.0% (male 31.9%, female 10.0%), respectively, which were all higher than that in urban Taiwanese. Comparing the three studies from the urban cities of northern, middle and southern Taiwan, we found that the overall prevalence of substance usage was higher in this indigenous group, especially in the females.
The prevalence rate of smoking among the indigenous group has been described in previous studies with 71.1% in males and 25.2% in females [19], 58.7% in males [20] and 33.3% overall [21], which were similar results compared with our study.
The higher prevalence rate of alcohol drinking and alcohol drinking habits among indigenous groups was observed from previous studies. The results from a few studies even found that the overall prevalence rate of alcohol drinking was 85.5% in males and 58.0% in females in an indigenous group of northern Taiwan [19] and 78.6% in males in an indigenous group of middle Taiwan [20]. Another study showed that the prevalence rates of alcohol drinking among northern, southern and eastern indigenous groups in Taiwan were 22.1%, 20.3% and 25.8%, respectively [16]. These results varied due to a different definition of an alcohol drinking habit; however, a higher prevalence rate of alcohol drinking in indigenous groups was observed.
The prevalence rates of betel nut chewing were 49.7% in males and 6.3% in females in an indigenous group of northern Taiwan [19] and 48.9% in males in an indigenous group of middle Taiwan [20]. Another study showed that the prevalence rates of alcohol drinking among northern, southern and eastern indigenous groups in Taiwan were 24.1%, 33.0% and 54.2%, respectively [16]. It seems that the prevalence rate of betel nut chewing was lower than other indigenous groups and the possible reasons need further investigation.
Previous studies have proved that smoking is related to atherosclerotic CVD, neoplastic, respiratory, osteoporosis and all-cause mortality [22]. An increased risk of metabolic syndrome among current smokers, particularly those with a heavier consumption, has also been reported [23]. Alcohol drinking has also been reported as a significant contributing factor to medical conditions such as hepatitis, hypertension, tuberculosis, pneumonia, pancreatitis and cardiomyopathy [24]. Heavy drinking, in particular among liquor drinkers, is associated with an increased risk of metabolic syndrome by influencing its components [25]. A previous systemic review found that betel nut chewing was a significant risk factor for metabolic syndrome [26]. Another study found that both raw areca nuts and those with tobacco additives had a harmful relationship with metabolic syndrome [27]. Although the exact mechanism that links betel nut chewing with metabolic syndrome remains unclear, a meta-analysis proposed that the link might be related to the effect on inflammation, on adipogenesis and on appetite [28].
As the prevalence rates of metabolic syndrome and substance usage were higher than urban Taiwanese, we would like to know if substance usage was one of the confounding factors to metabolic syndrome in this indigenous group. Therefore, we built regression models to observe the trend. After adjusting for age and gender, we found that in this indigenous group, betel nut chewing was one of the confounding factors rather than smoking or alcohol drinking, which was different from previous studies. A better income and better education were indicators of a lower risk of suffering from metabolic syndrome. A cross-sectional study [10] that involved 725 indigenous residents in middle Taiwan conducted in 2008 showed similar results in that the significant confounding factors for metabolic syndrome were being aged 41–64 years old with OR = 1.81 (95% CI: 1.14, 2.88), education level at elementary school with OR = 1.61 (95% CI: 1.07, 2.42), an alcohol drinking habit with OR = 1.42 (95% CI: 0.99, 2.06) and a betel nut chewing habit with OR = 1.59 (95% CI: 1.03, 2.47).
4.3. Biochemical Parameters of MetS
With regard to biochemical parameters, the model was significant in the abnormal uric acid level with OR = 2.31 (95% CI: 1.43, 3.74), the elevated AST level with OR = 1.68 (95% CI: 1.09, 2.61), an abnormal ALT level with OR = 2.32 (95% CI: 1.65, 3.97), an abnormal γ-GT level with OR = 2.56 (95% CI: 1.65, 3.97) and an abnormal creatinine level with OR = 4.82 (95% CI: 1.33, 17.40).
Furthermore, the multiple logistic regression model was significant in older age with OR = 1.03 (95% CI: 1.01, 1.04), better education with OR = 0.44 (95% CI: 0.24, 0.83), abnormal uric acid levels with OR = 2.06 (95% CI: 1.22, 3.48), abnormal ALT levels with OR = 2.02 (95% CI: 1.24, 3.29), abnormal γ-GT levels with OR = 1.86 (95% CI: 1.13, 3.07) and abnormal creatinine levels with OR = 5.38 (95% CI: 1.25, 23.10). Aging has been suggested to be one of the major confounding factors for metabolic syndrome [29] and this was also proved to be one of the significant confounding factors in our study. The different prevalence rates of metabolic syndrome among men and women differs from studies [30,31,32]. Although a few studies in Taiwan have suggested a higher prevalence rate in men [33,34], we found that there was no significant difference in the indigenous population we observed. A similar finding from other indigenous populations [10] suggested that the growing prevalence among women was not only found worldwide [35] but was especially obvious in the indigenous population in Taiwan.
In this indigenous group, we observed that elevated uric acid levels, ALT levels, γ-GT levels and creatinine levels were related to metabolic syndrome. Recent studies have provided new insights into the mechanisms by which uric acid stimulates fat accumulation in the liver. Therefore, elevated serum uric acid is a strong predictor of the development of a fatty liver as well as metabolic syndrome [36]. Uric acid levels are associated with parameters of insulin resistance and indices of inflammation; however, uric acid levels do not predict the incidence of metabolic syndrome independently [37]. Another study also concluded that the elevation of ALT levels especially in obese groups reflected insulin resistance and could be a marker of metabolic syndrome [38]. A study focusing on an indigenous group also found that an elevated γ-GT level was associated with a higher waist circumference and triglyceride levels, which was also highly associated with metabolic syndrome [39]. Metabolic syndrome was suggested to be an important risk factor for chronic kidney disease [40]; however, other studies have suggested that low serum creatinine is a predictor of type 2 DM and metabolic syndrome [41].
5. Conclusions
Our study demonstrated that the prevalence rates of metabolic syndrome and substance use were higher in the indigenous population compared with urban Taiwanese and especially in females. Metabolic syndrome has been demonstrated to be a common precursor to the development of type 2 DM and CVD [3] as well as a risk factor for all-cause mortality [4]. We found that metabolic syndrome in this indigenous population was associated with their education level, income and biochemical parameters such as uric acid, ALT, γ-GT and creatinine levels. Therefore, we conclude that the relative lower education level, income and medical inequality could be the possible contributing factors for metabolic syndrome in this indigenous population.
This study provided us with more thorough information about the health condition and lifestyle of this indigenous group so that we can arrange further intervention programs to improve indigenous health care in clinical practice.
Author Contributions
Conceptualization, Y.-H.C. and J.-Y.C.; methodology, W.-C.Y. and J.-Y.C.; software, S.Y.-H.C. and J.-Y.C.; validation, S.W.-N.U. and J.-Y.C.; formal analysis, S.Y.-H.C. and J.-Y.C.; investigation, Y.-C.T., W.-C.L. and J.-Y.C.; resources, W.-C.L. and J.-Y.C.; data curation, Y.-C.T. and J.-Y.C.; writing—original draft preparation, Y.-C.T.; writing—review and editing, Y.-C.T.; visualization, J.-Y.C.; supervision, S.W.-N.U. and J.-Y.C.; project administration, S.Y.-H.C. and J.-Y.C.; funding acquisition, Y.-C.T. and J.-Y.C. All authors have read and agreed to the published version of the manuscript.
Funding
We appreciate Chang Gung Memorial Hospital (grants CMRPG3F0761, CMRPG3F0762, CMRPG3F0763) for supporting this study.
Acknowledgments
We are grateful to Yang-Wei Gao of Gao-Yang-Wei Clinic, Ting-Chih Chang, Chia-Chin Lee, Tzu-Han Lin and Cheng-Hsien Kuo for their involvement in data collection.
Conflicts of Interest
The authors declare no conflict of interest.
Abbreviations
CVD, cardiovascular disease; DM, diabetes; ATP III, Adult Treatment Panel III; NCEP, National Cholesterol Education Program; CAP, College of American Pathologists; HDL, high-density lipoprotein cholesterol; ALT, alanine transaminase; AST, aspartate transaminase; γ-GT, Gamma-Glutamyl Transferase; HS-CRP, high sensitive C-reactive protein; HbA1c, glycohemoglobulin; LDL-C, low-density lipoprotein cholesterol; VLDL-C, very-low-density lipoprotein cholesterol.
References
- Eckel, R.H.; Alberti, K.G.; Grundy, S.M.; Zimmet, P.Z. The metabolic syndrome. Lancet 2010, 375, 181–183. [Google Scholar] [CrossRef]
- Alberti, K.G.; Eckel, R.H.; Grundy, S.M.; Zimmet, P.Z.; Cleeman, J.I.; Donato, K.A.; Fruchart, J.C.; James, W.P.; Loria, C.M.; Smith, S.C., Jr.; et al. Harmonizing the metabolic syndrome: A joint interim statement of the international diabetes federation task force on epidemiology and prevention; national heart, lung, and blood institute; american heart association; world heart federation; international atherosclerosis society; and international association for the study of obesity. Circulation 2009, 120, 1640–1645. [Google Scholar] [PubMed] [Green Version]
- 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., Jr.; 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. [Google Scholar] [CrossRef] [Green Version]
- Wu, S.H.; Liu, Z.; Ho, S.C. Metabolic syndrome and all-cause mortality: A meta-analysis of prospective cohort studies. Eur. J. Epidemiol. 2010, 25, 375–384. [Google Scholar] [CrossRef]
- Lin, I.C.; Yang, Y.W.; Wu, M.F.; Yeh, Y.H.; Liou, J.C.; Lin, Y.L.; Chiang, C.H. The association of metabolic syndrome and its factors with gallstone disease. BMC Fam. Pract. 2014, 15, 138. [Google Scholar] [CrossRef] [Green Version]
- Wu, T.W.; Chan, H.L.; Hung, C.L.; Lu, I.J.; Wang, S.D.; Wang, S.W.; Wu, Y.J.; Wang, L.Y.; Yeh, H.I.; Wei, Y.H.; et al. Differential patterns of effects of age and sex on metabolic syndrome in Taiwan: Implication for the inadequate internal consistency of the current criteria. Diabetes Res. Clin. Pract. 2014, 105, 239–244. [Google Scholar] [CrossRef] [PubMed]
- Pan, W.H.; Yeh, W.T.; Weng, L.C. Epidemiology of metabolic syndrome in Asia. Asia Pac. J. Clin. Nutr. 2008, 17 (Suppl. 1), 37–42. [Google Scholar] [PubMed]
- Liu, J.; Young, T.K.; Zinman, B.; Harris, S.B.; Connelly, P.W.; Hanley, A.J. Lifestyle variables, non-traditional cardiovascular risk factors, and the metabolic syndrome in an aboriginal Canadian population. Obesity 2006, 14, 500–508. [Google Scholar] [CrossRef] [PubMed]
- Huang, H.P.; Hsu, H.Y.; Chung, T.C.; Sun, C.A.; Chu, C.M.; Tang, T. An investigation of metabolic syndrome indicators among different ethnic groups—A case study from a health screening in Pingtung area. Taiwan J. Public Health 2008, 27, 250–258. [Google Scholar]
- Hung, L.L.; Hsiu, H.F.; Chen, M.L.; Chang, L.C.; Chen, C.Y.; Chen, C.M. The association between health risk behavior and metabolic syndrome of aborigines in Taiwan. Taipei City Med. J. 2010, 7, 255–264. [Google Scholar]
- Hsiao, Y.C.; Wang, K.; Bair, M.J. Prevalence of obesity and metabolic syndrome in aboriginals in Southeastern Taiwan–A hospital-based study. J. Intern. Med. Taiwan 2011, 22, 48–56. [Google Scholar]
- Robberecht, H.; Hermans, N. Biomarkers of metabolic syndrome: Biochemical background and clinical significance. Metab. Syndr. Relat. Disord. 2016, 14, 47–93. [Google Scholar] [CrossRef] [PubMed]
- Ahmad, O.B.; Boschi-Pinto, C.; Lopez, A.D.; Murray, C.J.; Lozano, R.; Inoue, M. Age standardization of rates: A new who standard. In GPE Discussion Paper Series: No.31; World Health Organization: Geneva, Switzerland, 2001. [Google Scholar]
- Liu, Y.M.; Chen, S.L.; Yen, A.M.; Chen, H.H. Individual risk prediction model for incident cardiovascular disease: A bayesian clinical reasoning approach. Int. J. Cardiol. 2013, 167, 2008–2012. [Google Scholar] [CrossRef] [PubMed]
- Yen, A.M.; Chen, S.L.; Chiu, S.Y.; Fann, J.C.; Wang, P.E.; Lin, S.C.; Chen, Y.D.; Liao, C.S.; Yeh, Y.P.; Lee, Y.C.; et al. A new insight into fecal hemoglobin concentration-dependent predictor for colorectal neoplasia. Int. J. Cancer 2014, 135, 1203–1212. [Google Scholar] [CrossRef]
- Liang, C.Y.; Chou, T.M.; Ho, P.S.; Shieh, T.Y.; Yang, Y.H. Prevanlence rates of alcohol drinking in Taiwan. Taiwan J. Oral. Med. Health Sci 2004, 20, 91–104. [Google Scholar]
- Kuo, C.J. Prevalence of alcoholism in a primary care setting. Taiwan. J. Psychiatry 2005, 19, 137–147. [Google Scholar]
- Lin, C.Y.; Chen, K.H.; Chang, H.Y.; Tseng, F.Y.; Chen, C.Y. The relationship between the pattern of alcohol consumption and healthcare utilization in Taiwan. Taiwan J. Public Health 2014, 33, 197–208. [Google Scholar]
- Liu, B.H.; Hsieh, S.F.; Chang, S.J.; Ko, Y.C. Prevalence of smoking, drinking and betel quid chewing and related factors among aborigines in Wufeng district. Gaoxiong Yi Xue Ke Xue Za Zhi 1994, 10, 405–411. [Google Scholar]
- Huang, L.L.; Chang, L.C.; Chen, M.L.; Hsi, H.F.; Chen, C.Y. Exploration on health-risk behavior and its related factors in aborigines. J. Chang Gung Inst. Technol. 2011, 14, 67–77. [Google Scholar]
- Yen, L.L.; Pan, L.Y.; Yen, H.W.; Lee, L.A. The smoking status in adults in Taiwan area: Prevalence rates and risk factors. Chin. J. Public Health 1994, 13, 371–380. [Google Scholar]
- Jha, P.; Ramasundarahettige, C.; Landsman, V.; Rostron, B.; Thun, M.; Anderson, R.N.; McAfee, T.; Peto, R. 21st-century hazards of smoking and benefits of cessation in the United States. N. Engl. J. Med. 2013, 368, 341–350. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- de Oliveira Fontes Gasperin, L.; Neuberger, M.; Tichy, A.; Moshammer, H. Cross-sectional association between cigarette smoking and abdominal obesity among Austrian bank employees. BMJ Open 2014, 4, e004899. [Google Scholar] [CrossRef] [Green Version]
- Zaridze, D.; Brennan, P.; Boreham, J.; Boroda, A.; Karpov, R.; Lazarev, A.; Konobeevskaya, I.; Igitov, V.; Terechova, T.; Boffetta, P.; et al. Alcohol and cause-specific mortality in Russia: A retrospective case-control study of 48,557 adult deaths. Lancet 2009, 373, 2201–2214. [Google Scholar] [CrossRef] [Green Version]
- Baik, I.; Shin, C. Prospective study of alcohol consumption and metabolic syndrome. Am. J. Clin. Nutr. 2008, 87, 1455–1463. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Javed, F.; Al-Hezaimi, K.; Warnakulasuriya, S. Areca-nut chewing habit is a significant risk factor for metabolic syndrome: A systematic review. J. Nutr. Health Aging 2012, 16, 445–448. [Google Scholar] [CrossRef] [PubMed]
- Shafique, K.; Zafar, M.; Ahmed, Z.; Khan, N.A.; Mughal, M.A.; Imtiaz, F. Areca nut chewing and metabolic syndrome: Evidence of a harmful relationship. Nutr. J. 2013, 12, 67. [Google Scholar] [CrossRef] [Green Version]
- Yamada, T.; Hara, K.; Kadowaki, T. Chewing betel quid and the risk of metabolic disease, cardiovascular disease, and all-cause mortality: A meta-analysis. PLoS ONE 2013, 8, e70679. [Google Scholar] [CrossRef] [Green Version]
- Ford, E.S.; Giles, W.H.; Dietz, W.H. Prevalence of the metabolic syndrome among US adults: Findings from the third national health and nutrition examination survey. JAMA 2002, 287, 356–359. [Google Scholar] [CrossRef]
- Fezeu, L.; Balkau, B.; Kengne, A.P.; Sobngwi, E.; Mbanya, J.C. Metabolic syndrome in a Sub-Saharan African setting: Central obesity may be the key determinant. Atherosclerosis 2007, 193, 70–76. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- He, Y.; Jiang, B.; Wang, J.; Feng, K.; Chang, Q.; Zhu, S.; Fan, L.; Li, X.; Hu, F.B. Bmi versus the metabolic syndrome in relation to cardiovascular risk in elderly Chinese individuals. Diabetes Care 2007, 30, 2128–2134. [Google Scholar] [CrossRef] [Green Version]
- Regitz-Zagrosek, V.; Lehmkuhl, E.; Mahmoodzadeh, S. Gender aspects of the role of the metabolic syndrome as a risk factor for cardiovascular disease. Gend. Med. 2007, 4 (Suppl. B), S162–S177. [Google Scholar] [CrossRef]
- Chuang, S.Y.; Chen, C.H.; Chou, P. Prevalence of metabolic syndrome in a large health check-up population in Taiwan. J. Chin. Med. Assoc. 2004, 67, 611–620. [Google Scholar]
- Hwang, L.C.; Bai, C.H.; Chen, C.J.; Chien, K.L. Gender difference on the development of metabolic syndrome: A population-based study in Taiwan. Eur. J. Epidemiol. 2007, 22, 899–906. [Google Scholar] [CrossRef] [PubMed]
- Ford, E.S.; Giles, W.H.; Mokdad, A.H. Increasing prevalence of the metabolic syndrome among U.S. Adults. Diabetes Care 2004, 27, 2444–2449. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Choi, Y.-J.; Shin, H.-S.; Choi, H.S.; Park, J.-W.; Jo, I.; Oh, E.-S.; Lee, K.-Y.; Lee, B.-H.; Johnson, R.J.; Kang, D.-H. Uric acid induces fat accumulation via generation of endoplasmic reticulum stress and SREBP-1c activation in hepatocytes. Lab. Investig. 2014, 94, 1114–1125. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ferrara, L.A.; Wang, H.; Umans, J.G.; Franceschini, N.; Jolly, S.; Lee, E.T.; Yeh, J.; Devereux, R.B.; Howard, B.V.; De Simone, G. Serum uric acid does not predict incident metabolic syndrome in a population with high prevalence of obesity. Nutr. Metab. Cardiovasc. Dis. 2014, 24, 1360–1364. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Abe, Y.; Kikuchi, T.; Nagasaki, K.; Hiura, M.; Tanaka, Y.; Ogawa, Y.; Uchiyama, M. Usefulness of gpt for diagnosis of metabolic syndrome in obese Japanese children. J. Atheroscler. Thromb. 2009, 16, 902–909. [Google Scholar] [CrossRef] [Green Version]
- Ho, C.I.; Tsao, Y.C.; Chen, J.Y.; Chang, K.C.; Tsai, Y.W.; Lin, J.S.; Chang, S.S. Gamma-glutamyl transpeptidase and the metabolic syndrome in a Taiwanese aboriginal population. Int. J. Diabetes Dev. Ctries. 2013, 33, 147–154. [Google Scholar] [CrossRef]
- Chen, J.; Gu, D.; Chen, C.S.; Wu, X.; Hamm, L.L.; Muntner, P.; Batuman, V.; Lee, C.H.; Whelton, P.K.; He, J. Association between the metabolic syndrome and chronic kidney disease in Chinese adults. Nephrol. Dial. Transpl. 2007, 22, 1100–1106. [Google Scholar] [CrossRef] [Green Version]
- Hjelmesaeth, J.; Roislien, J.; Nordstrand, N.; Hofso, D.; Hager, H.; Hartmann, A. Low serum creatinine is associated with type 2 diabetes in morbidly obese women and men: A cross-sectional study. BMC Endocr. Disord. 2010, 10, 6. [Google Scholar] [CrossRef] [Green Version]
Figure 1.
Geographical information of the remote area of the Fuxing District.
Table 1.
Background analysis of basic information, biomarkers and the prevalence of metabolic syndrome of the male and female population (n = 586).
Table 1.
Background analysis of basic information, biomarkers and the prevalence of metabolic syndrome of the male and female population (n = 586).
| Variables | Total | Male | Female | p-Value | ||||
|---|---|---|---|---|---|---|---|---|
| (n = 586) | (n= 275) | (n = 311) | (α = 0.05) | |||||
| Age | 49.3 | ±15.8 | 50.4 | ±16.9 | 48.4 | ±14.8 | 0.1217 | |
| Age | ||||||||
| <30 | 65 | (11.1) | 33 | (12.0) | 32 | (10.3) | 0.1361 | |
| 30–39 | 115 | (19.6) | 45 | (16.4) | 70 | (22.5) | ||
| 40–49 | 118 | (20.1) | 53 | (19.3) | 65 | (20.9) | ||
| 50–59 | 116 | (19.8) | 53 | (19.3) | 63 | (20.3) | ||
| 60–69 | 104 | (17.8) | 50 | (18.2) | 54 | (17.4) | ||
| >70 | 68 | (11.6) | 41 | (14.9) | 27 | (8.7) | ||
| Income (NTD, New Taiwan Dollars) | 0.0028 * | |||||||
| <10,000 | 295 | (61.3) | 114 | (53.8) | 181 | (67.3) | ||
| 10,000–29,999 | 140 | (29.1) | 69 | (32.6) | 71 | (26.4) | ||
| >30,000 | 46 | (9.6) | 29 | (13.7) | 17 | (6.3) | ||
| Unknown | 105 | 63 | 42 | |||||
| Education | 0.0382 * | |||||||
| ≤6 grade | 222 | (45.9) | 94 | (43.9) | 128 | (47.4) | ||
| 7–9 grade | 135 | (27.9) | 51 | (23.8) | 84 | (31.1) | ||
| 10–12 grade | 98 | (20.3) | 55 | (25.7) | 43 | (15.9) | ||
| College or higher | 29 | (6.0) | 14 | (6.5) | 15 | (5.6) | ||
| Unknown | 102 | 61 | 41 | |||||
| Current cigarette smoker | <0.0001 | |||||||
| No | 351 | (73.6) | 134 | (63.2) | 217 | (81.9) | ||
| Yes | 126 | (26.4) | 78 | (36.8) | 48 | (18.1) | ||
| Unknown | 109 | 63 | 46 | |||||
| Alcohol drinking habit | 0.0513 | |||||||
| No | 320 | (66.7) | 132 | (62.0) | 188 | (70.4) | ||
| Yes | 160 | (33.3) | 81 | (38.0) | 79 | (29.6) | ||
| Unknown | 106 | 62 | 44 | |||||
| Betel nut chewing habit | <0.0001 | |||||||
| No | 410 | (86.0) | 166 | (78.7) | 244 | (91.7) | ||
| Yes | 67 | (14.1) | 45 | (21.3) | 22 | (8.3) | ||
| Unknown | 109 | 64 | 45 | |||||
| DM | 0.1210 | |||||||
| No | 488 | (83.3) | 236 | (85.8) | 252 | (81.0) | ||
| Yes (FG ≥ 126 or with history) | 98 | (16.7) | 39 | (14.2) | 59 | (19.0) | ||
| Hypertension | 0.9494 | |||||||
| No | 281 | (50.6) | 131 | (50.8) | 150 | (50.5) | ||
| Yes (SBP ≥ 140 or DBP ≥ 90 or with history) | 274 | (49.4) | 127 | (49.2) | 147 | (49.5) | ||
| Unknown | 31 | 17 | 14 | |||||
| Metabolic syndrome | 0.4728 | |||||||
| No | 299 | (57.1) | 141 | (58.8) | 158 | (55.6) | ||
| Yes (ATP III Asian criteria) | 225 | (42.9) | 99 | (41.3) | 126 | (44.4) | ||
| Unknown | 62 | 35 | 27 | |||||
| Uric acid | <0.0001 | |||||||
| Normal | 475 | (81.1) | 198 | (72.0) | 277 | (89.1) | ||
| Abnormal (>8 mg/dL) | 111 | (18.9) | 77 | (28.0) | 34 | (10.9) | ||
| Total cholesterol | 0.0672 | |||||||
| Normal | 326 | (55.6) | 142 | (51.6) | 184 | (59.2) | ||
| Abnormal (≥200 mg/dL) | 260 | (44.4) | 133 | (48.4) | 127 | (40.8) | ||
| High-density lipoprotein cholesterol (HDL-C) | 0.0075 * | |||||||
| Normal | 385 | (65.7) | 196 | (71.3) | 189 | (60.8) | ||
| Abnormal (male < 40 or female < 50 mg/dL) | 201 | (34.3) | 79 | (28.7) | 122 | (39.2) | ||
| Triglyceride | 0.0453 * | |||||||
| Normal | 345 | (58.9) | 150 | (54.6) | 195 | (62.7) | ||
| Abnormal (≥150 mg/dL) | 241 | (41.1) | 125 | (45.5) | 116 | (37.3) | ||
| Aspartate transaminase (AST) | 0.2833 | |||||||
| Normal | 463 | (79.0) | 212 | (77.1) | 251 | (80.7) | ||
| Abnormal (>34 U/L) | 123 | (21.0) | 63 | (22.9) | 60 | (19.3) | ||
| Alanine transaminase (ALT) | 0.1390 | |||||||
| Normal | 463 | (79.0) | 210 | (76.4) | 253 | (81.4) | ||
| Abnormal (>36 U/L) | 123 | (21.0) | 65 | (23.6) | 58 | (18.7) | ||
| Gamma-Glutamyl Transferase (γ-GT) | 0.0019 * | |||||||
| Normal | 443 | (75.6) | 224 | (81.5) | 219 | (70.4) | ||
| Abnormal (Male > 71 or female > 42 U/L) | 143 | (24.4) | 51 | (18.6) | 92 | (29.6) | ||
| Creatinine | 0.2333 | |||||||
| Normal | 566 | (96.6) | 263 | (95.6) | 303 | (97.4) | ||
| Abnormal (Male > 1.27 or female > 1.02 mg/dL) | 20 | (3.4) | 12 | (4.4) | 8 | (2.6) | ||
| Hepatitis B surface antigen (HBsAg) | 0.6558 | |||||||
| Negative | 452 | (82.0) | 208 | (81.3) | 244 | (82.7) | ||
| Positive | 99 | (18.0) | 48 | (18.8) | 51 | (17.3) | ||
| Unknown | 35 | 19 | 16 | |||||
| Anti-HCV antibody | 0.2646 | |||||||
| Negative | 520 | (94.6) | 245 | (95.7) | 275 | (93.5) | ||
| Positive | 30 | (5.5) | 11 | (4.3) | 19 | (6.5) | ||
| Unknown | 36 | 19 | 17 | |||||
* p-Value < 0.05.
Table 2.
Crude and standardized prevalence of substance usage compared with other parts of Taiwan.
| Substance Use | Subjects | Fuxing District | Northern Taiwan 1 | Central Taiwan 1 | Southern Taiwan 1 | |
|---|---|---|---|---|---|---|
| Prevalence | Standardized Prevalence 1 | |||||
| Cigarette smoking | Total | 26.4 | 33.3 | 28.6 | 14.0 | 16.0 |
| Male | 36.8 | 45.3 | 59.1 | 53.7 | 52.3 | |
| Female | 18.1 | 25.9 | 9.4 | 2.5 | 2.7 | |
| Alcohol drinking | Total | 33.3 | 36.7 | 24.1 | 6.8 | 8.4 |
| Male | 38.0 | 39.1 | 47.6 | 23.7 | 27.9 | |
| Female | 29.6 | 35.0 | 9.4 | 1.7 | 1.7 | |
| Betel nut chewing | Total | 14.1 | 18.0 | 7.2 | 6.5 | 5.4 |
| Male | 21.3 | 31.9 | 18.1 | 28.9 | 23.3 | |
| Female | 8.3 | 10.0 | 0.8 | 0.3 | 0.4 | |
1 Standardized using the WHO 2000 world population, http://www.who.int/healthinfo/paper31.pdf. Total subjects: 586; male: 275, female: 311.
Table 3.
Results of univariate and multivariate regression models on possible variants comparing those with and without metabolic syndrome.
Table 3.
Results of univariate and multivariate regression models on possible variants comparing those with and without metabolic syndrome.
| Variables | Model 1 Univariate Regression | Model 2 Univariate Regression, Adjusted for Age and Gender | Model 3 Multivariate Regression, Adjusted for Age and Gender | ||||||
|---|---|---|---|---|---|---|---|---|---|
| OR | (95% CI) | p-Value | aOR | (95% CI) | p-Value | aOR (n = 524) | (95% CI) | p-Value | |
| Gender | |||||||||
| Female | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| Male | 0.88 | (0.62, 1.25) | 0.4728 | 0.81 | (0.57, 1.17) | 0.2587 | 0.76 | (0.50, 1.16) | 0.2029 |
| Age | 1.03 | (1.02, 1.04) | <0.0001 | 1.03 | (1.02, 1.04) | <.0001 | 1.03 | (1.01, 1.04) | 0.0006 * |
| Age (years old) | |||||||||
| <30 | 1.00 | Ref. | |||||||
| 30–39 | 2.12 | (0.96, 4.71) | 0.0648 | ||||||
| 40–49 | 4.99 | (2.29, 10.90) | <0.0001 | ||||||
| 50–59 | 5.99 | (2.74, 13.11) | <0.0001 | ||||||
| 60–69 | 7.47 | (3.39, 16.48) | <0.0001 | ||||||
| ≥70 | 4.52 | (1.96, 10.45) | 0.0004 * | ||||||
| Income (NTD, New Taiwan Dollars) | |||||||||
| <10,000 | 1.00 | Ref. | 1.00 | Ref. | |||||
| 10,000–29,999 | 0.47 | (0.31, 0.73) | 0.0006 * | 0.60 | (0.38, 0.94) | 0.0254 * | |||
| >30,000 | 0.44 | (0.22, 0.88) | 0.0207 * | 0.58 | (0.28, 1.17) | 0.1273 | |||
| Education | |||||||||
| ≤6 years | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| 7–9 years | 0.48 | (0.30, 0.76) | 0.0018 * | 0.68 | (0.40, 1.15) | 0.1538 | 0.59 | (0.34, 1.04) | 0.0676 |
| 10–12 years | 0.32 | (0.19, 0.54) | <0.0001 | 0.46 | (0.26, 0.83) | 0.0100 * | 0.44 | (0.24, 0.83) | 0.0103 * |
| >12 years | 0.33 | (0.14, 0.79) | 0.0126 * | 0.55 | (0.21, 1.41) | 0.2127 | 0.73 | (0.27, 1.97) | 0.5380 |
| Current cigarette smoker | |||||||||
| No | 1.00 | Ref. | 1.00 | Ref. | |||||
| Yes | 1.03 | (0.66, 1.61) | 0.9000 | 1.39 | (0.86, 2.23) | 0.1806 | |||
| Alcohol drinking habit | |||||||||
| No | 1.00 | Ref. | 1.00 | Ref. | |||||
| Yes | 1.30 | (0.86, 1.96) | 0.2081 | 1.51 | (0.99, 2.31) | 0.0558 | |||
| Betel nut chewing habit | |||||||||
| No | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| Yes | 1.52 | (0.87, 2.65) | 0.1432 | 2.21 | (1.22, 4.00) | 0.0087 * | 1.64 | (0.86, 3.13) | 0.1358 |
| Uric acid | |||||||||
| Normal | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| Abnormal (>8 mg/dL) | 1.93 | (1.24, 3.02) | 0.0039 * | 2.31 | (1.43, 3.74) | 0.0007 * | 2.06 | (1.22, 3.48) | 0.0071 * |
| Total cholesterol | |||||||||
| Normal | 1.00 | Ref. | 1.00 | Ref. | |||||
| Abnormal (≥200 mg/dL) | 1.65 | (1.16, 2.34) | 0.0052 * | 1.47 | (1.02, 2.12) | 0.0367 * | |||
| AST | |||||||||
| Normal | 1.00 | Ref. | 1.00 | Ref. | |||||
| Abnormal (>34 U/L) | 1.47 | (0.96, 2.24) | 0.0756 | 1.68 | (1.09, 2.61) | 0.0199 * | |||
| ALT | |||||||||
| Normal | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| Abnormal (>36 U/L) | 1.85 | (1.21, 2.83) | 0.0043 * | 2.32 | (1.49, 3.62) | 0.0002 * | 2.02 | (1.24, 3.29) | 0.0046 * |
| γ-GT | |||||||||
| Normal | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| Abnormal (Male > 71 or female > 42 U/L) | 2.06 | (1.36, 3.11) | 0.0006 * | 2.56 | (1.65, 3.97) | <0.0001 | 1.86 | (1.13, 3.07) | 0.0144 * |
| Creatinine | |||||||||
| Normal | 1.00 | Ref. | 1.00 | Ref. | 1.00 | Ref. | |||
| Abnormal (Male > 1.27 or female > 1.02 mg/dL) | 6.55 | (1.86, 23.06) | 0.0035 * | 4.82 | (1.33, 17.40) | 0.0164 * | 5.38 | (1.25, 23.10) | 0.0237 * |
| Hepatitis B surface antigen (HBsAg) | |||||||||
| Negative | 1.00 | Ref. | 1.00 | Ref. | |||||
| Positive | 0.77 | (0.49, 1.23) | 0.2726 | 0.79 | (0.49, 1.26) | 0.3163 | |||
| Anti-HCV antibody | |||||||||
| Negative | 1.00 | Ref. | 1.00 | Ref. | |||||
| Positive | 1.75 | (0.80, 3.81) | 0.1619 | 1.52 | (0.68, 3.37) | 0.3048 | |||
* p-Value < 0.05.
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Tsao, Y.-C.; Li, W.-C.; Yeh, W.-C.; Ueng, S.W.-N.; Chiu, S.Y.-H.; Chen, J.-Y. The Association between Metabolic Syndrome and Related Factors among the Community-Dwelling Indigenous Population in Taiwan. Int. J. Environ. Res. Public Health 2020, 17, 8958. https://doi.org/10.3390/ijerph17238958
AMA Style
Tsao Y-C, Li W-C, Yeh W-C, Ueng SW-N, Chiu SY-H, Chen J-Y. The Association between Metabolic Syndrome and Related Factors among the Community-Dwelling Indigenous Population in Taiwan. International Journal of Environmental Research and Public Health. 2020; 17(23):8958. https://doi.org/10.3390/ijerph17238958
Chicago/Turabian StyleTsao, Yu-Chung, Wen-Cheng Li, Wei-Chung Yeh, Steve Wen-Neng Ueng, Sherry Yueh-Hsia Chiu, and Jau-Yuan Chen. 2020. "The Association between Metabolic Syndrome and Related Factors among the Community-Dwelling Indigenous Population in Taiwan" International Journal of Environmental Research and Public Health 17, no. 23: 8958. https://doi.org/10.3390/ijerph17238958
APA StyleTsao, Y. -C., Li, W. -C., Yeh, W. -C., Ueng, S. W. -N., Chiu, S. Y. -H., & Chen, J. -Y. (2020). The Association between Metabolic Syndrome and Related Factors among the Community-Dwelling Indigenous Population in Taiwan. International Journal of Environmental Research and Public Health, 17(23), 8958. https://doi.org/10.3390/ijerph17238958
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