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Hypertriglyceridemic waist phenotype and associated factors in individuals with arterial hypertension and/or diabetes mellitus

Published online by Cambridge University Press:  14 September 2021

Luiza Delazari Borges*
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Luma de Oliveira Comini
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Laura Camargo de Oliveira
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Heloísa Helena Dias
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Emily de Souza Ferreira
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Clara Regina Santos Batistelli
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Glauce Dias da Costa
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Tiago Ricardo Moreira
Affiliation:
Departament of Nursing and Medicine, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
Rodrigo Gomes da Silva
Affiliation:
Clinical Director of the Hemodialysis Service, São João Batista Hospital, Viçosa, Minas Gerais, Brazil
Rosângela Minardi Mitre Cotta
Affiliation:
Department of Nutrition and Health, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil
*
*Corresponding author: Luiza Delazari Borges, email luizadelazarib@gmail

Abstract

Cardiovascular diseases are among the main causes of death in Brazil and worldwide. The literature indicates the hypertriglyceridemic waist phenotype (HTWP) as an accessible alternative for the identification of cardiovascular and metabolic risk. The present study aimed to identify the prevalence and factors associated with HTWP in individuals diagnosed with arterial hypertension (AH) and/or diabetes mellitus type 2 (DM2). A cross-sectional study was conducted with individuals diagnosed with AH and/or DM2. The study data were collected through semi-structured interviews containing socio-demographic information, lifestyle, health care, in addition to anthropometric assessment, blood pressure measurement and biochemical blood tests. The prevalence of HTWP was estimated and bivariate and multivariate logistic regression was used to assess the factors associated with HTWP. Of the 788 individuals analysed, 21⋅5 % had the HTWP. In the adjusted model, the following variables remained associated with a greater chance of presenting HTWP: sex, age, body mass index (BMI) and very-low-density lipoprotein (VLDL). Being female increased the chance of HTWP by 7⋅7 times (OR 7⋅7; 95 % CI 3⋅9, 15⋅2). The one-year increase in age increased the chance of HTWP by 4 % (OR 1⋅04; 95 % CI 1⋅02, 1⋅06). The addition of 1 mg/dl of VLDL-c increased the chance of HTWP by 15 % (odds ratio (OR) 1⋅15; 95 % confidence interval (CI) 1⋅12, 1⋅18), as well as the increase of 1 kg/m2 in the BMI increased the chance of this condition by 20 % (OR 1⋅20; 95 % CI 1⋅15, 1⋅27). The prevalence of HTWP was associated with females, older age, higher BMI, higher VLDL-c and risk waist/height ratio.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society

Introduction

Chronic non-communicable diseases (NCDs), especially cardiovascular diseases (CVDs), are the biggest cause of death in the world, causing approximately 31 % of all deaths globally. About the 17 million premature deaths caused by NCDs, 82 % occur in low- and middle-income countries, 37 % due to CVD. In Brazil, 31⋅2 % of deaths are caused by CVD(1).

Presently, for the diagnosis of abdominal adiposity, the waist–height ratio (WHR), and the waist perimeter (WP) is considered the best risk indicators for CVD(2Reference Rimm EB and Giovannucci6). The main risk factors for cardiovascular events are obesity, dyslipidemia, smoking, physical inactivity, high blood pressure and diabetes mellitus. As the risk factors are associated and added to each other, the possibility of the occurrence of cardiovascular events changes(7Reference Oliveira, Lopes and Peluzio9).

Thus, Lemieux and collaborators in 2000, proposed the hypertriglyceridemic waist phenotype (HTWP), which takes into account the simultaneous increase in WP and triglyceride levels, as an indicator for the identification of cardiovascular and metabolic risk(Reference Lemieux, Pascot and Couillard10,Reference Freitas, Fonseca and Schimidt11) . It is a low-cost method and easily applicable to the clinic and public health, presenting sensitivity and specificity to track individuals prone to develop CVD(Reference Lemieux, Pascot and Couillard10,Reference Freitas, Fonseca and Schimidt11) . Studies point out that the hypertriglyceridemic waist represents a discriminating phenotype to identify individuals characterised by an altered cardiovascular and metabolic risk profile(Reference Blackburn, Lemieux and Alméras12).

The present study aimed to identify the prevalence and factors associated with HTWP in individuals diagnosed with arterial hypertension (AH) and/or diabetes mellitus type 2 (DM2).

Experimental methods

Study design

A cross-sectional study, with a quantitative approach, carried out with individuals diagnosed with AH and/or DM2 accompanied by sixteen primary health care (PHC) teams from Viçosa, Minas Gerais, Brazil, a medium-sized municipality (approximately 78 381 inhabitants), according to the Brazilian Institute of Geography and Statistics(13).

Study participants

The selection of survey participants was made using the two-stage cluster sampling method, considering the population of 6624 hypertensive and/or diabetic individuals registered and monitored by the PHC in 2017(13). The sample was defined considering 50 % expected phenomenon prevalence, 5 % sampling error margin, 50 % conglomerate effect, 10 % refusals and/or losses, 20 % to control confounding factors and 95 % confidence level. The sample calculation was performed in the Statcalc (program of Epi-Info® version 7.2), and resulted in a sample of 840 individuals, corresponding to 12⋅68 % of the total.

Individuals diagnosed with AH and/or DM2 were chosen because they often present cardiovascular risk factors and coexisting metabolic complications, a characteristic condition of the metabolic syndrome.

The inclusion criteria of the present study were that the participants were 18 years old or older, had a diagnosis of AH and/or DM2, and were registered and monitored by the PHC teams. The study excluded individuals who had severe clinical conditions or who needed specialised care, pregnant women, individuals with a history of alcohol abuse and/or other drugs, bedridden, wheelchair users, people who were unable to go to the PHC unit location for data collection, and those who refused to participate in all stages of the study. Of the 840 individuals selected at random, 52 did not participate in all stages of the study, with a final sample of 788 participants.

This study was conducted in accordance with the Norms and Ethical Guidelines of the Resolution of the National Health Council 510/2016 of the Ministry of Health of Brazil and with the Declaration of Helsinki. The Research Ethics Committee of the Federal University of Viçosa under the number 1203173/2015 approved it. After the reading and signing of the Informed Consent Term, all participants were submitted to anamnesis, clinical, laboratory and anthropometric assessments.

Data collect

Data were collected in the PHC units between August 2017 and April 2018, through anthropometric assessment, blood pressure measurement, biochemical blood tests and a semi-structured interview guide, with socio-demographic (marital status, age, years of study, colour/race and work), clinic (systolic (SBP) and diastolic blood pressure (DBP)), lifestyle (alcohol and tobacco use) and health care information.

The dependent variable was the HTWP, which is characterised by the simultaneous presence of WC, and triacylglycerols increased. WC was measured immediately above the iliac crest, adopting the cut-off point of the National Cholesterol Education Program (NCEP)(2), and of the World Health Organization (WHO)(14), which classifies as inadequate, values ≥88 cm for women and ≥102 cm for men. Triglyceride values ≥150 mg/dl were considered high. The independent variables were age in years, marital status, colour, work, education in years, number of medications used, alcoholism, tobacco, underlying diseases, self-reported infarction and stroke, diagnosed CKD, number of medications used, body mass index (BMI), glycosylated haemoglobin, fasting blood glucose, total cholesterol, HDL-cholesterol, LDL-cholesterol, VLDL-cholesterol, serum phosphorus, serum calcium, SBP and DBP.

The clinical examination included SBP and DBP and anthropometric measurement. Blood pressure was measured and classified according to the procedures recommended by the VII Brazilian Hypertension Guidelines of 2016(15). AH was defined as SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg and, or current use of antihypertensive medications(15). Trained researchers, using standard protocols and techniques obtained the anthropometric measurements that consisted of weight, height, BMI, hip circumference (HC) and WHR. The weight was obtained using an electronic scale, with a capacity of 150 kg and a division of 50 g; height was measured using a portable anthropometer, consisting of a metal platform for positioning individuals and a removable wooden column containing millimeter tape and a reading cursor, according to the techniques proposed by Jellife(Reference Jelliffe16). BMI was calculated using the relationship between weight and height squared (P/E2). The WC was measured using an inextensible tape and measured in centimetres.

Statistical analysis

To characterise the study population regarding the variables under study, a descriptive analysis was performed. The normality of the distribution of the continuous variables was tested using the Kolmogorov–Smirnov test. The prevalence of HTWP was estimated, and its association with the characteristics of the individuals was investigated using the χ 2 test for categorical variables and the parametric test (Student's t) or non-parametric test (Mann–Whitney) for continuous variables according to the result normality test. For all tests, the significance level was set at 95 %.

The strength of the association between the HTWP and the explanatory variables was assessed using the odds ratio and their respective 95 % confidence intervals using bivariate and multivariate logistic regression.

In the multivariate analysis, the adjusted analysis method used was backward elimination due to likelihood (Wald test). In this sense, all variables that lost their significance were removed from the model one at a time as they did not present significance in the adjustment. Only variables with P < 0⋅10 remained in the adjusted model. All analyses were performed using the SPSS program (Statistical Package for Social Science, version 22; SPSS Inc., Chicago, USA).

Results

Of the 788 individuals analysed, 62⋅7 % were female, 62⋅7 % were married and 43⋅9 % were self-declared brown, yellow or indigenous. The median age was 62 years. Regarding lifestyle habits, 11⋅7 % were smokers, and 27⋅8 % used alcohol. Most individuals reported never having suffered a heart attack (94⋅3 %), stroke (93⋅5 %) and 84⋅5 % reported the presence of CKD. Among the basic diseases, 36⋅3 % have AH and DM2, 55⋅8 % only AH and 7⋅9 % DM2. Other characteristics of interests are presented in Table 1.

Table 1. Descriptive and univariate analysis of socio-demographic, clinical, anthropometric and lifestyle habits associated with HTWP

HTWP, hypertriglyceridemic waist phenotype.

* Statistically significant results.

The prevalence of HTWP found was 21⋅5 % (95 % CI), being higher in women (82⋅2 %), in individuals of brown, yellow or indigenous colour, who presented hypertension, DM2 and CKD (Table 1). The prevalence was also higher in participants who use more medications and have higher values of BMI, glycosylated haemoglobin, fasting glucose, total cholesterol, VLDL, calcium, phosphorus and SBP. In the group with HTWP, HDL was lower (Table 2).

Table 2. Descriptive and univariate analysis of socio-demographic, clinical, anthropometric, lifestyle and biochemical characteristics associated with HTWP

HDL-c, high-density lipoprotein-cholesterol; HTWP, hypertriglyceridemic waist phenotype; LDL-c, low-density lipoprotein-cholesterol; VLDL-c, very-low-density lipoprotein-cholesterol.

a Median (IR).

b Average (sd).

* Statistically significant results.

In the adjusted model, the following variables remained associated with the HTWP: sex, age, risk WHR, BMI and VLDL. Being female increases the chance of developing HTWP by 7⋅7 times (odds ratio (OR) 7⋅7; 95 % confidence interval (CI) 3⋅9, 15⋅2). Having a risk WHR increases the chance of HTWP by 3⋅8 times (OR 3⋅83; 95 % CI 1⋅94, 7⋅60). The increase of one year in age increased this chance of HTWP by 4 % (OR 1⋅04; 95 % CI 1⋅02, 1⋅06). The addition of 1 mg/dl of VLDL-c increased the chance of HTWP by 15 % (OR 1⋅15; 95 % CI 1⋅12, 1⋅18), as well as the 1 kg/m2 increased in BMI, which increased the chance of this condition by 20 % (OR 1⋅20; 95 % CI 1⋅15, 1⋅27) (Table 3).

Table 3. Crude and adjusted analysis of socio-demographic, clinical, anthropometric, lifestyle and biochemical factors associated with HTWP

Initially, all variables from the crude analysis were included in the multivariate analysis, but only those with P < 0⋅10 by the Wald test remained in the model.

CI, Confidence interval; HTWP, hypertriglyceridemic waist phenotype; OR, odds ratio; VLDL-c, very-low-density lipoprotein-cholesterol.

Discussion

A prevalence of 21⋅5 % of HTWP was found. The presence of HTWP remained associated with females, older age, higher BMI, higher VLDL-c and with risk WHR. The present study points out the HTWP as a viable cardiovascular and metabolic risk indicator option to be inserted in clinical practice, as it only involves the measurement of two simple and low-cost measures.

In the ELSA-Brazil study, the prevalence of HTWP was between 13⋅3 % and 24⋅7 %, according to the classification of the WC used (NCEP or International Diabetes Federation [IDF]), which confirms the present study. The literature shows that regardless of the cut-off point used, which is defined through the location of the WC measurement, the HTWP is associated with cardiovascular and metabolic risk factors(Reference Freitas, Fonseca and Schimidt11). In another study carried out with adults and using the NCEP cut-off points, the prevalence of HTWP was 26⋅7 %, a result higher than the present study(Reference Poirier, Kubow and Noël17). There were also records of lower prevalence in adult populations, such as that reported in a study in Viçosa-MG of 17⋅32 %(Reference Rocha AL, Pereira and Pessoa18) and a study in southern Brazil(Reference Haack, Horta and Gigante19) indicating 5⋅9 % and 4⋅5 % among men and women, respectively, with an average age of 23 years. Mendes et al. (Reference Mendes20) still found a prevalence of 21⋅4 %, a result very similar to the present study, however, its screened population was only obese.

The presence of HTWP has numerous implications, including obesity, which is presently the second leading cause of preventable death in Western countries, consequently, there is an increase in visceral fat(Reference Mendes20) due to the high correlation between BMI and WC(Reference Oliveira, Lopes and Peluzio9). This fact corroborates with the results of the present study due to the finding of a significant association between increased BMI and the presence of HTWP and also with studies conducted in Brazil(Reference Oliveira, Lopes and Peluzio9,Reference Mendes20) and with a population-based cohort from China(Reference Wang, Li and Zhou21), indicating that individuals with HTWP have an accumulation of adiposity global and not just in the abdominal region.

The relationship between obesity, high BMI and changes in lipid metabolism, which, in turn, can result in accumulation of these in the liver, muscle, and in the adipose tissue itself is consolidated in the literature(Reference Oliveira, Lopes and Peluzio9). In this way, there is a picture of factors associated with each other that generate damage to the population's health. The results of the present study corroborate this finding by demonstrating the association between an increase in VLDL-c with the chance of presenting HTWP. Similar results were found in other study with adult population in Brazil(Reference Freitas, Fonseca and Schimidt11).

In parallel with obesity, visceral adipose tissue and dyslipidemic changes, HTWP can also be associated with the development of CVDs, increased c-reactive protein, increased oxidative stress, insulin resistance and high blood pressure(Reference Oliveira, Lopes and Peluzio9,Reference Mendes20Reference Solati, Ghanbarian and Rahmani22) . HTWP is an effective and less invasive method to identify individuals susceptible to developing CVDs(Reference Mendes20).

The female sex was associated with HTWP. This result differs from others, which mostly shown that there was no difference between the genders(Reference Freitas, Fonseca and Schimidt11,Reference Poirier, Kubow and Noël17Reference Mendes20) . In a study carried out in South America, more cases of HTWP were observed among men (38⋅1 %) than among women (30⋅3 %). Another study reported that the risk of fatal cardiovascular events increased 4⋅7-fold in postmenopausal women with high levels of triacylglycerols, which corroborates with the present study where the majority of women were in postmenopause. The result of the European Prospective Research on Cancer and Nutrition (EPIC)-Norfolk also indicated a greater association of HTWP with females(Reference Arsenault, Lemieux and Despres23).

Mendes et al. (Reference Mendes20), when analysing a population in the interior of Brazil, found an association between HTWP and increasing on age (OR 1⋅028; 95 % CI 1⋅006, 1⋅052), the same results were found by Freitas et al. (Reference Freitas, Fonseca and Schimidt11) (P < 0⋅001) and in the present study. These findings are explained by the physiology of aging, which leads to metabolic changes that result in the presence of HTWP(Reference Mendes20).

The study's limitations include the type of design and the lack of consensus in the literature regarding the definition of the best method to measure the WC, which is directly linked to the HTWP. Thus, there is a need for further studies on this topic. Another limitation is the non-inclusion of important variables to confirm possible associations with HTWP, such as long-term diet, physical activity and sleep habits. As for the strengths of the study, we highlight the representative sample of the population and the use of a database built from a survey with methodological quality, which guarantees the reliability of the data.

The prevalence of HTWP found in the study was high (21⋅5 %) and was associated with females, older age, higher BMI and higher VLDL-c. HTWP is an easily applicable indicator, so its use should be encouraged in health services to predict and decrease the risk of cardiovascular events. It is important to investigate different indicators of cardiovascular and metabolic risk to insert and execute them in practice. The prevention and early treatment of CVDs must be a priority of health policies aiming at health promotion and disease prevention.

Acknowledgements

L. D. B. designed the study, analysed the data, interpreted the results of the study, writing of the manuscript and prepared the final version of the article for publication. L. O. C., L. C. O., H. H. D. and C. R. S. B. contributed to designed the study, the interpretation of results, writing of the manuscript and final approval of the manuscript for submission; T. R. M. and R. M. M. C. supervised the data analysis, contributed to the writing and revision of the manuscript and approved the final manuscript for submission; E. S. F., G. D. C. and R. G. S. contributed to the writing of the manuscript and final approval of the manuscript for submission. All authors read and approved the final manuscript.

The present study was supported by the Minas Gerais Research Support Foundation (FAPEMIG) for the research project entitled ‘Prevention of diseases and diseases in patients with arterial hypertension in the context of primary health care: chronic renal disease on the agenda’. Process Number: CSA-APQ-03510-13.

The authors declare that they have no competing interests.

References

World Health Organization (WHO) (2018) Global Status Report on Noncommunicable Disease. Geneva: World Health Organization (WHO).Google Scholar
Executive summary of the third report of The National Cholesterol Education Program (NCEP) (2001) Expert Panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). JAMA 285, 24862497.CrossRefGoogle Scholar
Janssen, I, Katzmarzyk, PT & Ross, R (2004) Waist circumference and not body mass index explains obesity-related health risk. Am J Clin Nutr 79, 379384.CrossRefGoogle Scholar
Larsson, B, Svardsudd, K, Welin, L, et al. (1984) Abdominal adipose tissue distribution, obesity, and risk of cardiovascular disease and death:13-year follow-up of participants in the study of men born in 1913. Br Med J (Clin Res Ed) 288, 14011404.CrossRefGoogle Scholar
Oppert, JM, Charles, MA, Thibult, N, et al. (2002) Anthropometric estimates of muscle and fat mass in relation to cardiac and cancer mortality in men: the Paris Prospective Study. Am J Clin Nutr 75, 11071113.CrossRefGoogle ScholarPubMed
Rimm EB, S, Giovannucci, E, et al. (1995) Body size and fat distribution as predictors of coronary heart disease among middle-aged and older US men. Am J Epidemiol 141, 11171127.CrossRefGoogle ScholarPubMed
World Health Organization (WHO) (2000) Obesity: preventing and managing the global epidemic. Report of a WHO consultation. World Health Organ Tech Rep Ser 894, 1253 [i–xii].Google Scholar
Pozzan, R, Pozzan, R, Magalhães, MEC, et al. (2003) O conceito de estratificação de risco para eventos coronarianos na abordagem da dislipidemia. Rev SOCERJ 16, 194203.Google Scholar
Oliveira, JL, Lopes, LL, Peluzio, MCG, et al. (2014) Fenótipo cintura hipertrigliceridêmica e risco cardiometabólico em indivíduos dislipidêmicos. Rev Bras Cardiol 27, 395402.Google Scholar
Lemieux, I, Pascot, A, Couillard, C, et al. (2000) Hypertriglyceridemic waist: a marker of the atherogenic metabolic triad (hyperinsulinemia; hyperapolipoprotein B; small, dense LDL) in men? Circulation 102, 179184.CrossRefGoogle ScholarPubMed
Freitas, RS, Fonseca, MJM, Schimidt, MI, et al. (2018) Fatores associados ao fenótipo de cintura hipertrigliceridêmica. Cad Saúde Pública 34, e00067617.Google Scholar
Blackburn, P, Lemieux, I, Alméras, N, et al. (2009) The hypertriglyceridemic waist phenotype versus the National Cholesterol Education Program-Adult Treatment Panel III and International Diabetes Federation clinical criteria to identify high-risk men with an altered cardiometabolic risk profile. Metabolism 58, 11231130.CrossRefGoogle ScholarPubMed
DAB – Departamento de Atenção Básica (2018) Informação e Gestão da Atenção Básica e-Gestor. Cobertura da Atenção Básica. Sudeste, Minas Gerais, Viçosa. Disponívelem: https://egestorab.saude.gov.br/paginas/acessoPublico/relatorios/relHistoricoCoberturaAB.xhtmlGoogle Scholar
World Health Organization (WHO) (1998) Obesity: Preventing and Managing the Global Epidemic. Report of a WHO Consultation on Obesity. Geneva: World Health Organization (WHO).Google Scholar
Sociedade Brasileira de Cardiologia (2016) VII diretrizes Brasileiras de Hipertensão. Arq Bras Cardiol 107, 183.Google Scholar
Jelliffe, DBI (1968) Evaluación del estado de nutrición de la comunidad. Geneva: World Health Organization (WHO).Google Scholar
Poirier, J, Kubow, S, Noël, M, et al. (2015) The hypertriglyceridemic-waist phenotype is associated with the Framingham risk score and subclinical atherosclerosis in Canadian Cree. Nutr Metab Cardiovasc Dis 25, 10501055.CrossRefGoogle ScholarPubMed
Rocha AL, C, Pereira, PF, Pessoa, MC, et al. (2015) Hypertriglyceridemic waist phenotype and cardiometabolic alterations in Brazilian adults. Nutr Hosp 32, 10991106.Google Scholar
Haack, RL, Horta, BL, Gigante, DP, et al. (2013) The hypertriglyceridemic waist phenotype in young adults from the southern region of Brazil. Cad Saúde Pública 29, 9991007.CrossRefGoogle ScholarPubMed
Mendes, MSF (2009) Cintura hipertrigliceridêmica e sua associação com fatores de risco metabólicos. Dissertação de Mestrado, Universidade Federal de Minas Gerais, Belo Horizonte.Google Scholar
Wang, A, Li, Z, Zhou, Y, et al. (2014) Hypertriglyceridemic waist phenotype and risk of cardiovascular diseases in China: results from the Kailuan Study. Int J Cardiol 174, 106109.CrossRefGoogle ScholarPubMed
Solati, M, Ghanbarian, A, Rahmani, M, et al. (2004) Cardiovascular risk factors in males with hypertriglycemic waist (Tehran lipid and glucose study). Int J Obes Relat Metab Disord 28, 706709.CrossRefGoogle Scholar
Arsenault, BJ, Lemieux, I, Despres, JP, et al. (2010) The hypertriglyceridemic-waist phenotype and the risk of coronary artery disease: results from the EPIC-Norfolk prospective population study. CMAJ 182, 14271432.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Descriptive and univariate analysis of socio-demographic, clinical, anthropometric and lifestyle habits associated with HTWP

Figure 1

Table 2. Descriptive and univariate analysis of socio-demographic, clinical, anthropometric, lifestyle and biochemical characteristics associated with HTWP

Figure 2

Table 3. Crude and adjusted analysis of socio-demographic, clinical, anthropometric, lifestyle and biochemical factors associated with HTWP