Acessibilidade / Reportar erro

Clustering and combining pattern of metabolic syndrome components in a rural Brazilian adult population

Agregação e padrão de combinação dos componentes da síndrome metabólica em uma população rural adulta brasileira

Abstracts

CONTEXT AND OBJECTIVE

Metabolic syndrome is characterized by clustering of cardiovascular risk factors such as obesity, dyslipidemia, insulin resistance, hyperinsulinemia, glucose intolerance and arterial hypertension. The aim of this study was to estimate the probability of clustering and the combination pattern of three or more metabolic syndrome components in a rural Brazilian adult population.

DESIGN AND SETTING

This was a cross-sectional study conducted in two rural communities located in the Jequitinhonha Valley, Minas Gerais, Brazil.

METHODS

The sample was composed of 534 adults (both sexes). Waist circumference, blood pressure and demographic, lifestyle and biochemical characteristics were assessed. The prevalences of metabolic syndrome and its components were estimated using the definitions of the National Cholesterol Education Program – Adult Treatment Panel III. A binomial distribution equation was used to evaluate the probability of clustering of metabolic syndrome components. The statistical significance level was set at 5% (P < 0.05).

RESULTS

Metabolic syndrome was more frequent among women (23.3%) than among men (6.5%). Clustering of three or more metabolic syndrome components was greater than expected by chance. The commonest combinations of three metabolic syndrome components were: hypertriglyceridemia + low levels of HDL-c + arterial hypertension and abdominal obesity + low levels of HDL-c + arterial hypertension; and of four metabolic syndrome components: abdominal obesity + hypertriglyceridemia + low levels of HDL-c + arterial hypertension.

CONCLUSION

The population studied presented high prevalence of metabolic syndrome among women and clustering of its components greater than expected by chance, suggesting that the combination pattern was non-random.

Metabolic syndrome x; Risk factors; Rural population; Cluster analysis; Obesity, abdominal


CONTEXTO E OBJETIVO

A síndrome metabólica é caracterizada pela agregação de fatores de risco cardiovasculares como obesidade, dislipidemia, resistência à insulina, hiperinsulinemia, intolerância à glicose e hipertensão arterial. Este estudo objetivou estimar a probabilidade de agregação e o padrão de combinação de três ou mais componentes da síndrome metabólica em população rural adulta brasileira.

TIPO DE ESTUDO E LOCAL

Estudo transversal, conduzido em duas comunidades rurais da região do Vale do Jequitinhonha, Minas Gerais.

MÉTODOS

A amostra foi constituída de 534 adultos, de ambos os sexos, dos quais foram aferidas a circunferência da cintura, a pressão arterial e características demográficas, do estilo de vida e bioquímicas. Prevalências da síndrome metabólica e seus componentes foram estimados usando a definição da National Cholesterol Education Program – Adult Treatment Panel III. A equação da distribuição binomial foi utilizada para avaliar a probabilidade de agregação dos componentes da síndrome metabólica. O nível de significância estatística estabelecido foi 5% (P < 0,05).

RESULTADOS

Síndrome metabólica foi mais frequente em mulheres (23,3%) que homens (6,5%). A agregação de três ou mais componentes da síndrome metabólica foi maior do que esperada ao acaso. Combinações mais comuns para três componentes da síndrome metabólica foram hipertrigliceridemia + baixos níveis de HDL-c + hipertensão arterial, obesidade abdominal + baixos níveis de HDL-c + hipertensão arterial. Para quatro componentes, obesidade abdominal + hipertrigliceridemia + baixos níveis de HDL-c + hipertensão arterial.

CONCLUSÃO

Na população estudada, a prevalência da síndrome metabólica foi alta entre mulheres e houve agregação dos seus componentes acima do esperado que ocorra ao acaso, sugerindo padrão não aleatório de combinação.

Síndrome x metabólica; Fatores de risco; População rural; Análise por conglomerados; Obesidade abdominal


INTRODUCTION

Metabolic syndrome is characterized by clustering of cardiovascular risk factors such as obesity, dyslipidemia, insulin resistance, hyperinsulinemia, glucose intolerance and hypertension.11. Cornier MA, Dabelea D, Hernandez TL, et al. The metabolic syndrome. Endocr Rev. 2008;29(7):777-822. This syndrome is recognized as an important public health problem worldwide, due to prevalence greater than 20.0% in adult populations living both in urban and in rural areas,22. Ford ES. The metabolic syndrome and mortality from cardiovascular disease and all-causes: findings from the National Health and Nutrition Examination Survey II Mortality Study. Atherosclerosis. 2004;173(2):309-14.77. Kim TN, Kim JM, Won JC, et al. A decision tree-based approach for identifying urban-rural differences in metabolic syndrome risk factors in the adult Korean population. J Endocrinol Invest. 2012;35(9):847-52. and also to its strong association with cardiovascular diseases and type 2 diabetes, which are both major causes of death worldwide.11. Cornier MA, Dabelea D, Hernandez TL, et al. The metabolic syndrome. Endocr Rev. 2008;29(7):777-822.,88. Lawes CM, Vander Hoorn S, Rodgers A, International Society of Hypertension. Global burden of blood-pressure-related disease, 2001. Lancet. 2008;371(9623):1513-8.99. Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care. 2004;27(5):1047-53.

Despite this epidemiological context, the management of metabolic syndrome in clinical practice remains controversial,1010. Kahn R, Buse J, Ferrannini E, et al. The metabolic syndrome: time for a critical appraisal: joint statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2005;28(9):2289-304.,1111. Reaven GM. The metabolic syndrome: is this diagnosis necessary? Am J Clin Nutr. 2006;83(6):1237-47. primarily because of the random clustering of its components. Moreover, metabolic syndrome is diagnosed based upon the presence of three or more components out of a total of five,1212. Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001;285(19):2486-97. which could lead to a plethora of combination patterns.1313. Kuk JL, Ardern CI. Age and sex differences in the clustering of metabolic syndrome factors: association with mortality risk. Diabetes Care. 2010;33(11):2457-61. These various combinations require different interventions and therapeutic approaches, and this is often neglected in clinical practice.1313. Kuk JL, Ardern CI. Age and sex differences in the clustering of metabolic syndrome factors: association with mortality risk. Diabetes Care. 2010;33(11):2457-61. Nonetheless, accurate management of metabolic syndrome, in order to control the current global epidemics of cardiovascular disease and diabetes mellitus, is of fundamental importance.1414. Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112(17):2735-52.

In Brazil, these issues have been poorly investigated, particularly in rural areas, given that studies have usually focused on the prevalence of metabolic syndrome and associated factors in urban populations. Furthermore, there may be a need for different approaches towards evaluating metabolic syndrome in rural populations, which are also highly affected by this pathological condition44. Oliveira EP, Souza MLA, Lima MDA. Prevalência de síndrome metabólica em uma área rural do semi-árido baiano [Prevalence of metabolic syndrome in a semi-arid rural area in Bahia]. Arq Bras Endocrinol Metabol. 2006;50(3):456-65.,55. Gregory CO, Dai J, Ramirez-Zea M, Stein AD. Occupation is more important than rural or urban residence in explaining the prevalence of metabolic and cardiovascular disease risk in Guatemalan adults. J Nutr. 2007;137(5):1314-9.,77. Kim TN, Kim JM, Won JC, et al. A decision tree-based approach for identifying urban-rural differences in metabolic syndrome risk factors in the adult Korean population. J Endocrinol Invest. 2012;35(9):847-52. and thus would benefit from interventions such as establishing preventive strategies and adequate treatment.

OBJECTIVE

The objective of the present study was to estimate the probability of clustering and the combining pattern of three or more metabolic syndrome components in a rural Brazilian adult population.

METHODS

Study population and design

A cross-sectional population-based study was conducted between November 2004 and March 2005 in two communities, Virgem das Graças and Caju, in the rural areas of the municipalities of Ponto dos Volantes and Jequitinhonha, respectively. These communities are located in the Jequitinhonha Valley, in the northeast of the state of Minas Gerais, Brazil.

In other projects conducted in these areas, a census performed by our research group in 2001 showed that 1216 individuals were living in these communities. For the present study, 621 of these subjects were excluded due to the following criteria: age less than 18 years (n = 522); emigration (n = 33); death (n = 6); pregnancy (n = 14); diabetes diagnosis (n = 12); polymerase chain reaction values above 10 mg/l [which could indicate acute infection or inflammation] (n = 31);1515. Pearson TA, Mensah GA, Alexander RW, et al. Markers of inflammation and cardiovascular disease: application to clinical and public health practice: A statement for healthcare professionals from the Centers for Disease Control and Prevention and the American Heart Association. Circulation. 2003;107(3):499-511. and physical impossibilities that compromised anthropometric measurements (n = 3). Moreover, 61 individuals were also lost because of their absence at the time of the survey (n = 47) or refusal to participate (n = 14). Finally, data from 534 participants remained available for analysis.

Ethics committee approval

This study was approved by the Research Ethics Committee of Universidade Federal de Minas Gerais (UFMG), in accordance with National Health Council Resolution 196/96. All of the subjects who took part in the study were informed about the objectives of the research and their rights as participants, and then were asked to sign a consent form.

Data collection

An interview was conducted by nurses, in which the participants answered a survey questionnaire covering various aspects of their demographic characteristics (sex, age, skin color, marital status and schooling) and lifestyle characteristics (smoking habits and alcohol consumption). At the conclusion of the interview, a clinical evaluation was performed on the participants, which included waist circumference and blood pressure measurements, carried out in triplicate by well-trained staff in accordance with standard procedures.1616. Lohman TG, Roche AF, Martorell R. Anthropometric standardization reference manual. Champaign: Human Kinetics Books; 1988.

Blood samples were collected from each participant by means of venous puncture following a fasting period of 12 hours. Serum and plasma aliquots were obtained by centrifugation of each sample, and were appropriately treated and stored in vials maintained at 4 °C until arrival at the laboratory for biochemical analysis, in accordance with the recommended technical specifications for avoiding damage to biological material.

Colorimetric enzymatic methods were used to determine glucose, triglyceride and total cholesterol values using a Roche Cobas Mira Plus analyzer (Roche Diagnostics, Switzerland). The high-density lipoprotein cholesterol (HDL-c) concentration was also determined by means of colorimetric enzymatic assay, following precipitation of the low-density lipoprotein cholesterol (LDL-c) and very low-density lipoprotein cholesterol (VLDL-c) fractions, using phosphotungstic acid and magnesium chloride. The LDL-c concentrations were calculated by applying the Friedewald equation,1717. Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972;18(6):499-502. since there were no triglyceride values > 400 mg/dl: LDL-c = total cholesterol – (HDL-c + triglycerides/5).

Waist circumference was measured to the nearest millimeter, using a non-extendable measuring tape, and this was done exactly halfway between the margin of the lowest rib and the iliac crest, with participants in a standing position (accurate to 0.1 cm).1616. Lohman TG, Roche AF, Martorell R. Anthropometric standardization reference manual. Champaign: Human Kinetics Books; 1988.

Blood pressure was measured by means of an indirect method, using a sphygmomanometer (mercury manometer), in accordance with the Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure.1818. Chobanian AV, Bakris GL, Black HR, et al. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. JAMA. 2003;289(19):2560-72. Measurements were made three times in each participant's right arm with two-minute intervals between measurements, after an initial resting period of at least five minutes.

Definition of metabolic syndrome

Metabolic syndrome was diagnosed in accordance with the definition of the National Cholesterol Education Program - Adult Treatment Panel III (NCEP-ATP III), which requires the presence of three or more of the following components:1212. Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001;285(19):2486-97.

  1. Abdominal obesity: waist circumference ≥ 102 cm for men and ≥ 88 cm for women.

  2. Hypertriglyceridemia: triglycerides ≥ 150 mg/dl;

  3. Low HDL-c: HDL-c < 40 mg/dl for men and < 50 mg/dl for women;

  4. Hyperglycemia: fasting blood glucose ≥ 100 mg/dl.1414. Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112(17):2735-52.

  5. Arterial hypertension: systolic blood pressure ≥ 130 mmHg and/or diastolic blood pressure (DBP) ≥ 85 mmHg and/or hypertension treatment.

Statistical analyses

The study population characteristics were presented in terms of the absolute and relative frequencies of the demographic and lifestyle variables, stratified by sex. These same procedures were used to present the prevalence of metabolic syndrome and its components. Statistical differences were evaluated by means of Pearson's chi-square test, and the significance level was set at 5% (P < 0.05).

The analyses on clustering of three or more metabolic syndrome components, independently of their cutoff points, were performed based on the quintile distribution of each factor according to sex. Thus, a given component was determined to be present in an individual if he or she had values in the lowest quintile for HDL-c and the highest quintile for the other factors.

The expected degree of clustering of three or more metabolic syndrome components was estimated by calculating the probability of d occurrences for n factors, where the probability of each occurrence was 0.20 (extreme quintile). Individual probabilities were calculated from the binomial formula presented below.1919. Snedecor GW, Cochran WG. Statistical methods. 6th ed. Ames: Iowa State University Press; 1967.

Finally, the expected probability was compared with the observed proportion of subjects in the highest quintile for three or more metabolic syndrome components, using the Pearson chisquare test.

In addition, the proportions of three or more metabolic syndrome component combinations were also calculated stratified by sex. Statistical differences were evaluated by means of the Pearson chi-square test, and the significance level was set at 5% (P < 0.05).

All the analyses were performed using the Statistical Package for the Social Sciences (SPSS) software package for Windows, version 15.0 (SPSS Inc., Chicago, IL, United States).

RESULTS

The study population was composed of 270 men (50.6%) and 264 women (49.4%). The major demographic and lifestyle characteristics of the subjects, according to sex, are shown in Table 1. The age intervals among the population presented homogenous distribution, with a slightly higher proportion of individuals with ages between 18 and 29 years. Most of the subjects lived with a spouse (69.3%) and were of mixed/black color (75.3%). This last characteristic was observed more frequently among men. The proportion of individuals with less than five years of schooling was high (76.3%), as was the proportion of illiterates (34.5%). The prevalences of alcohol consumption and smoking habit were 23.6% and 30.3%, respectively. These habits were also more frequent among men.

Table 1.
Study population distribution according to demographic and lifestyle characteristics, stratified by sex. Virgem das Graças and Caju, 2004-2005

The prevalence of metabolic syndrome and its components, according to sex, are shown in Table 2. Metabolic syndrome was diagnosed in 14.9% of the participants, and was four times more frequent among women than among men (P < 0.05). Concerning metabolic syndrome components, 11.6% of the population presented abdominal obesity, 15.2% hypertriglyceridemia, 44.1% low levels of HDL-c, 10.6% hyperglycemia and 59.7% hypertension. Abdominal obesity and low levels of HDL-c were proportionally higher among women (P < 0.05).

Table 2.
Prevalence of metabolic syndrome and its components according to sex. Virgem das Graças and Caju, 2004-2005

Graph 1 presents the observed and expected frequencies of metabolic syndrome components, according to sex. Observed rates are represented by bars while expected rates are represented by lines. The observed frequencies were calculated based on the quintile distribution of metabolic syndrome components and are therefore not identical to the ones shown in Table 2. The expected frequencies were calculated in order to ascertain the nature of the co-occurrence of metabolic syndrome components and were based on the binomial distribution equation. Thus, for both sexes, the clustering of three or more metabolic syndrome components did not occur by chance, since the observed frequency (14.7% for men and 16.0% for women) was higher than the expected frequency (10.2%) ( Table 2). Additionally, these proportions were statistically tested and, in fact, this confirmed the differences between the observed and expected proportions (P-value < 0.05).

Graph 1.
Observed (bar) and expected (line) proportions of individuals for each number of metabolic syndrome components, according to sex. Virgem das Graças and Caju, 2004-2005

Table 3 shows the combinations of metabolic syndrome components among the individuals who presented this condition, according to sex. The most common combinations of three components in the population studied were hypertriglyceridemia + low levels of HDL-c + hypertension, and abdominal obesity + low levels of HDL-c + hypertension. The first pattern was more frequent among men and the second, among women. The most frequent combination of four components was abdominal obesity + hypertriglyceridemia + low levels of HDL-c + hypertension. This pattern was also more common among women. On the other hand, the most frequent four-component-pattern presented by men was hypertriglyceridemia + low levels of HDL-c + hyperglycemia + hypertension.

Table 3.
Combinations of metabolic syndrome components among the participants with this condition, according to sex. Virgem das Graças and Caju, 2004-2005

DISCUSSION

In this study, the prevalence of metabolic syndrome was 14.9%. The degree of clustering of its components was higher than what would be expected by chance and standard combinations between them.

Although the magnitude of the metabolic syndrome was not as high as what was observed in other studies conducted in both urban and rural areas, which was over 20%,22. Ford ES. The metabolic syndrome and mortality from cardiovascular disease and all-causes: findings from the National Health and Nutrition Examination Survey II Mortality Study. Atherosclerosis. 2004;173(2):309-14.77. Kim TN, Kim JM, Won JC, et al. A decision tree-based approach for identifying urban-rural differences in metabolic syndrome risk factors in the adult Korean population. J Endocrinol Invest. 2012;35(9):847-52. metabolic syndrome is an important public health concern in the study population, since these two communities are located in one of the poorest regions of Brazil. Alternatively, in analyses stratified by sex, the data have demonstrated high prevalence of metabolic syndrome among women (23.3%) and low prevalence among men (6.5%). Similar findings have also been shown in studies developed in rural areas in Brazil44. Oliveira EP, Souza MLA, Lima MDA. Prevalência de síndrome metabólica em uma área rural do semi-árido baiano [Prevalence of metabolic syndrome in a semi-arid rural area in Bahia]. Arq Bras Endocrinol Metabol. 2006;50(3):456-65. and other countries.55. Gregory CO, Dai J, Ramirez-Zea M, Stein AD. Occupation is more important than rural or urban residence in explaining the prevalence of metabolic and cardiovascular disease risk in Guatemalan adults. J Nutr. 2007;137(5):1314-9.,2020. Aekplakorn W, Kessomboon P, Sangthong R, et al. Urban and rural variation in clustering of metabolic syndrome components in the Thai population: results from the fourth National Health Examination Survey 2009. BMC Public Health. 2011;11:854. There seems to be a pattern of metabolic syndrome occurrence in rural areas that is characterized by higher prevalence among women. This phenomenon might be determined by people's occupations in this region, which differ greatly according to sex. Men still perform the field activities that require high energy expenditure, while women are devoted to housework.55. Gregory CO, Dai J, Ramirez-Zea M, Stein AD. Occupation is more important than rural or urban residence in explaining the prevalence of metabolic and cardiovascular disease risk in Guatemalan adults. J Nutr. 2007;137(5):1314-9. Another investigation developed using the same population as in this study showed that men were more active than women in relation to leisure, commuting and work, while women were more active than men in the household domain.2121. Bicalho PG, Hallal PC, Gazzinelli A, Knuth AG, Velásquez-Meléndez G. Atividade física e fatores associados em adultos de área rural em Minas Gerais, Brasil [Adult physical activity levels and associated factors in rural communities of Minas Gerais State, Brazil]. Rev Saude Publica. 2010;44(5):884-93.

We observed in this study that there were occurrences of three or more metabolic syndrome components at rates greater than would be predicted by chance. This may be indicative of the existence of underlying mechanisms that contribute towards these cluster patterns. This is an important finding, since not all associations among the components have been fully elucidated, thus leading researchers to ask whether the proposed definitions used to diagnose metabolic syndrome might only be random cardiovascular risk factors.1010. Kahn R, Buse J, Ferrannini E, et al. The metabolic syndrome: time for a critical appraisal: joint statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2005;28(9):2289-304.,1111. Reaven GM. The metabolic syndrome: is this diagnosis necessary? Am J Clin Nutr. 2006;83(6):1237-47. Similar results were found in an investigation conducted on a sample of 4,975 subjects aged between 18 and 74 years from the Framingham Offspring Study, which was an urban population. In that study, it was also pointed out that clustering of three or more cardiovascular risk factors (high levels of total cholesterol, low levels of HDL-c, hypertriglyceridemia, overall obesity, elevated systolic blood pressure and hyperglycemia) occurred at a rate greater than what would be expected by chance and, hence, there ought to be a connection between them.2222. Wilson PW, Kannel WB, Silbershatz H, D'Agostino RB. Clustering of metabolic factors and coronary heart disease. Arch Intern Med. 1999;159(10):1104-09. In other studies conducted on urban populations, it has also been demonstrated that combinations of three or more metabolic syndrome components occurred more frequently than the expected by chance.2323. Stagnaro S. Epidemiological evidence for the non-random clustering of the components of the metabolic syndrome: multicentre study of the Mediterranean Group for the Study of Diabetes. Eur J Clin Nutr. 2007;61(9):1143-4.2525. Ramachandran A, Snehalatha C, Latha E, Satyavani K, Vijay V. Clustering of cardiovascular risk factors in urban Asian Indians. Diabetes Care. 1998;21(6):967-71.

Physicians and researchers have been recognizing that cardiovascular disease determinants tend to cluster, and therefore the risk of developing these illnesses rises in line with increases in their clustering abilities.2626. Genest J Jr, Cohn JS. Clustering of cardiovascular risk factors: targeting high-risk individuals. Am J Cardiol. 1995;76(2):8A-20A.2828. Katakami N, Kaneto H, Matsuhisa M, et al. Clustering of several cardiovascular risk factors affects tissue characteristics of the carotid artery. Atherosclerosis. 2008;198(1):208-13. Therefore, our results corroborate those found in other investigations, thus providing greater consistency regarding the affirmation that metabolic syndrome is clinically useful as a diagnostic tool. Our results also show that, in the rural population studied, the occurrence of clustering of metabolic syndrome components was systematic and not random, thereby reinforcing the hypothesis that underlying pathophysiological mechanisms are involved in this process.

One important criticism of the clinical importance of metabolic syndrome relates to the fact that it is diagnosed based on the presence of three or more components out of a total of five. This creates the possibility of 16 combinations, with different pathophysiological patterns and, consequently, multiple treatment options,1313. Kuk JL, Ardern CI. Age and sex differences in the clustering of metabolic syndrome factors: association with mortality risk. Diabetes Care. 2010;33(11):2457-61. although we only found 13 among the studied population. Additionally, longitudinal studies have demonstrated variations in the risk of mortality according to the different combination patterns of metabolic syndrome components.2929. Guize L, Thomas F, Pannier B, et al. All-cause mortality associated with specific combinations of the metabolic syndrome according to recent definitions. Diabetes Care. 2007;30(9):2381-7.,3030. Hong Y, Jin X, Mo J, et al. Metabolic syndrome, its preeminent clusters, incident coronary heart disease and all-cause mortality--results of prospective analysis for the Atherosclerosis Risk in Communities study. J Intern Med. 2007;262(1):113-22. In our study, we observed that the most frequent combination of three components was hypertriglyceridemia + low levels of HDL-c + arterial hypertension among men and abdominal obesity + low levels of HDL-c + arterial hypertension among women, while the most common combination of four components was abdominal obesity + hypertriglyceridemia + low levels of HDL-c + arterial hypertension, for the whole study population. These combination patterns are similar to those found in other studies that also used the NCEP-ATP III metabolic syndrome definition.1313. Kuk JL, Ardern CI. Age and sex differences in the clustering of metabolic syndrome factors: association with mortality risk. Diabetes Care. 2010;33(11):2457-61.,2020. Aekplakorn W, Kessomboon P, Sangthong R, et al. Urban and rural variation in clustering of metabolic syndrome components in the Thai population: results from the fourth National Health Examination Survey 2009. BMC Public Health. 2011;11:854.,3131. Zaliūnas R, Slapikas R, Babarskiene R, et al. The prevalence of the metabolic syndrome components and their combinations in men and women with acute ischemic syndromes. Medicina (Kaunas). 2008;44(7):521-8.3333. Liu J, Zhao D, Wang W, et al. [Incidence risk of cardiovascular diseases associated with specific combinations regarding the metabolic syndrome components]. Zhonghua Liu Xing Bing Xue Za Zhi. 2008;29(7):652-5. As a result, it seems that the factors of real relevance in clinical practice are the combination patterns of metabolic syndrome components, according to sex. Consequently, healthcare professionals' conduct could be guided by these characteristics.

Furthermore, it could be seen that the most frequent combination patterns of metabolic syndrome components in most of the study population were abdominal obesity and dyslipidemia (hypertriglyceridemia and/or low levels of HDL-c). It was only in the pattern of hypertriglyceridemia + low levels of HDL-c + arterial hypertension that co-occurrence of abdominal obesity and dyslipidemia was not observed. On the other hand, this pattern was more frequent among men with an anthropometric profile consisting of low proportions of overall and abdominal obesity, thereby corroborating the findings of other studies.1313. Kuk JL, Ardern CI. Age and sex differences in the clustering of metabolic syndrome factors: association with mortality risk. Diabetes Care. 2010;33(11):2457-61.,2020. Aekplakorn W, Kessomboon P, Sangthong R, et al. Urban and rural variation in clustering of metabolic syndrome components in the Thai population: results from the fourth National Health Examination Survey 2009. BMC Public Health. 2011;11:854. Obesity, especially the abdominal or visceral type, plays a fundamental role in the pathophysiological mechanism of metabolic syndrome, given that it triggers the insulin resistance pathway as result of excessive free fatty acid accumulation in the blood circulation.11. Cornier MA, Dabelea D, Hernandez TL, et al. The metabolic syndrome. Endocr Rev. 2008;29(7):777-822.,3434. Eckel RH, Grundy SM, Zimmet PZ. The metabolic syndrome. Lancet. 2005;365(9468):1415-28.

We believe that our findings have a social impact because the study population was still undergoing the process of epidemiological transition, i.e. high rates of morbidity and mortality due to infectious and parasitic diseases3535. Reis DC, Kloos H, King C, et al. Accessibility to and utilisation of schistosomiasis-related health services in a rural area of state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz. 2010;105(4):587-97. were observed to coexist with increased occurrence of non-communicable illnesses.3636. Silva DA, Felisbino-Mendes MS, Pimenta AM, et al. Distúrbios metabólicos e adiposidade em uma população rural [Metabolic disorders and adiposity in a rural population]. Arq Bras Endocrinol Metabol. 2008;52(3):489-98. Moreover, the local health services are poor, thus hindering the population's access to actions aimed at health promotion and disease prevention, control and treatment.3535. Reis DC, Kloos H, King C, et al. Accessibility to and utilisation of schistosomiasis-related health services in a rural area of state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz. 2010;105(4):587-97.

Thus, this evidence of clustering and combination patterns of metabolic syndrome components contributes towards the existing knowledge. It corroborates the usefulness of metabolic syndrome as a diagnostic tool with simple clinical-laboratory criteria that are easily applicable at the primary health care level, including isolated rural areas in one of the poorest regions of Brazil.

This study has the following limitations: a) the sample was selected according to convenience, which means that caution is required in interpreting the external validity of our findings; b) the total number of individuals with a positive diagnosis of metabolic syndrome was small (n = 73), which needs to be taken into consideration in evaluating component combination patterns.

CONCLUSION

The rural population studied here presented high prevalence of metabolic syndrome among women. The metabolic syndrome components presented clustering at a rate greater than what would be expected by chance, suggesting that the combination patterns were non-random. The patterns that were most frequently observed were the following: hypertriglyceridemia + low levels of HDL-c + arterial hypertension; abdominal obesity + low levels of HDL-c + arterial hypertension; and abdominal obesity + hypertriglyceridemia + low levels of HDL-c + arterial hypertension.

REFERENCES

  • 1
    Cornier MA, Dabelea D, Hernandez TL, et al. The metabolic syndrome. Endocr Rev. 2008;29(7):777-822.
  • 2
    Ford ES. The metabolic syndrome and mortality from cardiovascular disease and all-causes: findings from the National Health and Nutrition Examination Survey II Mortality Study. Atherosclerosis. 2004;173(2):309-14.
  • 3
    Dutra ES, de Carvalho KM, Miyazaki E, Hamann EM, Ito MK. Metabolic syndrome in central Brazil: prevalence and correlates in the adult population. Diabetol Metab Syndr. 2012;4(1):20.
  • 4
    Oliveira EP, Souza MLA, Lima MDA. Prevalência de síndrome metabólica em uma área rural do semi-árido baiano [Prevalence of metabolic syndrome in a semi-arid rural area in Bahia]. Arq Bras Endocrinol Metabol. 2006;50(3):456-65.
  • 5
    Gregory CO, Dai J, Ramirez-Zea M, Stein AD. Occupation is more important than rural or urban residence in explaining the prevalence of metabolic and cardiovascular disease risk in Guatemalan adults. J Nutr. 2007;137(5):1314-9.
  • 6
    Zubair N, Kuzawa CW, McDade TW, Adair LS. Cluster analysis reveals important determinants of cardiometabolic risk patterns in Filipino women. Asia Pac J Clin Nutr. 2012;21(2):271-281.
  • 7
    Kim TN, Kim JM, Won JC, et al. A decision tree-based approach for identifying urban-rural differences in metabolic syndrome risk factors in the adult Korean population. J Endocrinol Invest. 2012;35(9):847-52.
  • 8
    Lawes CM, Vander Hoorn S, Rodgers A, International Society of Hypertension. Global burden of blood-pressure-related disease, 2001. Lancet. 2008;371(9623):1513-8.
  • 9
    Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care. 2004;27(5):1047-53.
  • 10
    Kahn R, Buse J, Ferrannini E, et al. The metabolic syndrome: time for a critical appraisal: joint statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2005;28(9):2289-304.
  • 11
    Reaven GM. The metabolic syndrome: is this diagnosis necessary? Am J Clin Nutr. 2006;83(6):1237-47.
  • 12
    Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001;285(19):2486-97.
  • 13
    Kuk JL, Ardern CI. Age and sex differences in the clustering of metabolic syndrome factors: association with mortality risk. Diabetes Care. 2010;33(11):2457-61.
  • 14
    Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112(17):2735-52.
  • 15
    Pearson TA, Mensah GA, Alexander RW, et al. Markers of inflammation and cardiovascular disease: application to clinical and public health practice: A statement for healthcare professionals from the Centers for Disease Control and Prevention and the American Heart Association. Circulation. 2003;107(3):499-511.
  • 16
    Lohman TG, Roche AF, Martorell R. Anthropometric standardization reference manual. Champaign: Human Kinetics Books; 1988.
  • 17
    Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972;18(6):499-502.
  • 18
    Chobanian AV, Bakris GL, Black HR, et al. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. JAMA. 2003;289(19):2560-72.
  • 19
    Snedecor GW, Cochran WG. Statistical methods. 6th ed. Ames: Iowa State University Press; 1967.
  • 20
    Aekplakorn W, Kessomboon P, Sangthong R, et al. Urban and rural variation in clustering of metabolic syndrome components in the Thai population: results from the fourth National Health Examination Survey 2009. BMC Public Health. 2011;11:854.
  • 21
    Bicalho PG, Hallal PC, Gazzinelli A, Knuth AG, Velásquez-Meléndez G. Atividade física e fatores associados em adultos de área rural em Minas Gerais, Brasil [Adult physical activity levels and associated factors in rural communities of Minas Gerais State, Brazil]. Rev Saude Publica. 2010;44(5):884-93.
  • 22
    Wilson PW, Kannel WB, Silbershatz H, D'Agostino RB. Clustering of metabolic factors and coronary heart disease. Arch Intern Med. 1999;159(10):1104-09.
  • 23
    Stagnaro S. Epidemiological evidence for the non-random clustering of the components of the metabolic syndrome: multicentre study of the Mediterranean Group for the Study of Diabetes. Eur J Clin Nutr. 2007;61(9):1143-4.
  • 24
    Aizawa Y, Watanabe H, Ramadan MM, et al. Clustering trend of components of metabolic syndrome. Int J Cardiol. 2007;121(1):117-8.
  • 25
    Ramachandran A, Snehalatha C, Latha E, Satyavani K, Vijay V. Clustering of cardiovascular risk factors in urban Asian Indians. Diabetes Care. 1998;21(6):967-71.
  • 26
    Genest J Jr, Cohn JS. Clustering of cardiovascular risk factors: targeting high-risk individuals. Am J Cardiol. 1995;76(2):8A-20A.
  • 27
    Yusuf HR, Giles WH, Croft JB, Anda RF, Casper ML. Impact of multiple risk factor profiles on determining cardiovascular disease risk. Prev Med. 1998;27(1):1-9.
  • 28
    Katakami N, Kaneto H, Matsuhisa M, et al. Clustering of several cardiovascular risk factors affects tissue characteristics of the carotid artery. Atherosclerosis. 2008;198(1):208-13.
  • 29
    Guize L, Thomas F, Pannier B, et al. All-cause mortality associated with specific combinations of the metabolic syndrome according to recent definitions. Diabetes Care. 2007;30(9):2381-7.
  • 30
    Hong Y, Jin X, Mo J, et al. Metabolic syndrome, its preeminent clusters, incident coronary heart disease and all-cause mortality--results of prospective analysis for the Atherosclerosis Risk in Communities study. J Intern Med. 2007;262(1):113-22.
  • 31
    Zaliūnas R, Slapikas R, Babarskiene R, et al. The prevalence of the metabolic syndrome components and their combinations in men and women with acute ischemic syndromes. Medicina (Kaunas). 2008;44(7):521-8.
  • 32
    Chen W, Srinivasan SR, Elkasabany A, Berenson GS. Cardiovascular risk factors clustering features of insulin resistance syndrome (Syndrome X) in a biracial (Black-White) population of children, adolescents, and young adults: the Bogalusa Heart Study. Am J Epidemiol. 1999;150(7):667-74.
  • 33
    Liu J, Zhao D, Wang W, et al. [Incidence risk of cardiovascular diseases associated with specific combinations regarding the metabolic syndrome components]. Zhonghua Liu Xing Bing Xue Za Zhi. 2008;29(7):652-5.
  • 34
    Eckel RH, Grundy SM, Zimmet PZ. The metabolic syndrome. Lancet. 2005;365(9468):1415-28.
  • 35
    Reis DC, Kloos H, King C, et al. Accessibility to and utilisation of schistosomiasis-related health services in a rural area of state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz. 2010;105(4):587-97.
  • 36
    Silva DA, Felisbino-Mendes MS, Pimenta AM, et al. Distúrbios metabólicos e adiposidade em uma população rural [Metabolic disorders and adiposity in a rural population]. Arq Bras Endocrinol Metabol. 2008;52(3):489-98.
  • This paper forms part of the thesis “Fatores associados à síndrome metabólica em área rural de Minas Gerais”, presented to the School of Nursing, Universidade Federal de Minas Gerais (UFMG), on December 15, 2008
  • Publication Dates

    • Publication in this collection
      2013

    History

    • Reviewed
      26 June 2011
    • Received
      31 Aug 2012
    • Accepted
      26 Nov 2012
    Associação Paulista de Medicina - APM APM / Publicações Científicas, Av. Brigadeiro Luís Antonio, 278 - 7º and., 01318-901 São Paulo SP - Brazil, Tel.: +55 11 3188-4310 / 3188-4311, Fax: +55 11 3188-4255 - São Paulo - SP - Brazil
    E-mail: revistas@apm.org.br