Keywords Metabolic syndrome; Children; Adolescent
Introduction Currently, obesity is seen as an epidemic of global proportion [1] and is associated with the increase of risk for many diseases and premature death [2]. Its interaction with other systemic and metabolic diseases increases organic disturbances significantly [3]. Among the several pathologies which are associated with obesity, Metabolic Syndrome (MS) has attracted the attention of health specialists. Recent studies revealed that population sets which contain a greater number of MS are those formed by obese individuals [3-5] and this metabolic disturbance is present in developed countries as well as developing countries, with a high rate of prevalence among the adult population e increasing prevalence in the pediatric population [6,7].
Historical Aspects and Definition MS has been observed since the 19th Century, receiving several names down through the years [8]. The first observations related to the syndrome occurred in the 1920s [9]. In 1923, Swedish doctor Eskil Kylin observed the association between hyperglycemia, obesity and the uric acid in the joints, known as gout, in hypertensive individuals [10]. In 1965, Avogaro et al. [11] described the metabolic aspects of obesity and mentioned a syndrome called plurimetabolic [11]. However, since 1979 there was greater understanding concerning an important component of MS, which is the Insulin Resistance (IR) [12,13]. In 1980, MS was called Syndrome X by Reaven, and since the studies of Reaven and Hoffman the involvement of IR and hyperinsulinemia in hypertension [14,15] etiology was verified. Reaven also discussed the relationship of IR to the concentration of Free Fatty Acids (FFA) and progressed in the hypothesisthat IR was a central mechanism in MS [16]. Finally, in a classic article published on the subject in 1988, this author proposed that a collection of diverse risk factors, connected by a common link could compose the syndrome which was then called MS [17]. After clarifying the boundaries which characterize MS, he went on to define it as a collection of risk factors of metabolic origin that appears to be directly related to the development of atherosclerosis and cardiovascular disease [18-20]. Among these risk factors are unfavorable lipid profile, hypertension, elevated plasmatic glucose, pro-thrombotic states, proinflammatory [21] and obesity, mainly abdominal [22].
Epidemiology The prevalence of MS has increased drastically in the last years, transforming it into an event of global proportions, similar to the obesity proportions. As such, there is believed to be a connection between MS and obesity [21]. The confirmation of this suspicion may be exemplified in a study which says that approximately 60% of participants with moderate obese (BMI of approximately 35 kg/m2) presented MS, although less than 6% of normal-weight adults met the criteria for the metabolic syndrome, affirming that normal-weight population may also met the criteria for MS [23]. Evidences indicate between 20 and 30% of the adult population can be diagnosed with MS [21]. In the United States, the prevalence of overweight children and adolescents is 6.8% and obesity is 28.7% and in the pediatric population of Brazil, Ferreira (2007) revealed the prevalence of MS to be 17.3% in obese children aged 7 to 10. The prevalence of MS varies depending on the diagnostic criteria used, since different health organizations develop different ways to diagnose MS, not counting other factors which can influence its rise, such as ethnicity and age [5,24]. A study performed on the American population, verified the prevalence of MS to be 22% in adults, 42% in individuals between 60 and 69 years [25], suggesting that age appears to have an influence on the development of MS. According to a European study DECODE (Diabetes Epidemiology: Collaborative Analysis of Diagnostic Criteria in Europe) there is a significant increase in death by all causes and cardiovascular complications in individuals with MS [26]. Similar data has been presented in studies using the British, Scandinavian, and American population [27-30].
Current Criteria for Diagnosing Metabolic Syndrome Criteria used for each one of the risk factors which characterize MS are referred to, mainly, in regards to their etiology, clinical importance of the diagnosis and physiopathological mechanisms involved in MS [31] and consequently there is no consensus in regards to MS diagnosis. Due to this variety of diagnostic criteria, there are difficulties in establishing what the global prevalence of MS is. Each criteria takes into consideration different risk factors, our different reference values, and studies show that the same sample evaluated by different criteria can present a wide variation in regards to prevalence [32]. Grundy [21] in a review study collected the data regarding the prevalence of MS in populations in different regions in the world and used different criteria, showing the high prevalence of MS in the global population, and the difference in prevalence in the same populations when using different criteria. The numbers presented by Grundy [21] can be observed in Table 1, in which is presented studies performed throughout Europe, in Table 2, studies in Asian populations and in Table 3, studies in Latin America. The situation is even more complex when dealing with children and adolescents, because of the lack of consensus about the MS diagnosis in infancy that could be accepted by the whole scientific community. Different criteria currently used for the parameters related to metabolic syndrome were published in varied well-known organizations in the area of health. In 1999, the World Health Organization (WHO) published their definition of MS [11] and two years later the National Cholesterol Education Program and Adult Treatment Panel III (NCEP-ATP III) [33] in the United States also published their own criteria. In Brazil, the 1st Brazilian Guidelines for Metabolic Syndrome Diagnosis and Treatment [34], published in 2004 by the Brazilian Hypertension Society based on the definition proposed by NCEP-ATP III [33]. The following year, the BrazilianCardiology Society proposed the I Guideline for Prevention of Atherosclerosis in Infancy and Adolescence [35] thereby providing reference values of the same components present in former directives, regarding MS, but specific for children and adolescents. Aiming to standardize the MS diagnostic criteria for children and adolescents, the International Diabetes Federation (IDF) [36] in 2007 also released a definition according to age groups, thus establishing values which could be used for anthropometric delineation, pressure and sanguinary biochemicals, to be applied to children and adolescents between 10 and 19 years [35]. Children under the age of 6 were excluded from definition, not having sufficient data for this age group. IDF does not recommend the diagnosis of MS in children under the age of ten, however it suggests monitoring the abdominal circumference and following the other risk factors in case there is family history with MS, Diabetes Mellitus type 2, dyslipidemia, heart disease, hypertension and/or obesity. In this criteria, for youth between 10 and 16 years of age, the reference values are the same as proposed by adults, with the exception of waist circumference whose percentiles rather than absolute values have been used to compensate for varying degrees of development and ethnicity, being considered as having excess of central fat the ones who present a circumference greater than 90th percentile. It is important to clarify that for all the age groups, central obesity is an essential condition to diagnose MS, in other words, the diagnosis requires the presence of central obesity plus two or more of the other risk factors. The reason to the using of waist circumference as a central obesity measure in IDF criteria is the impractical determination of insulin resistance in clinical practice and its strong correlation with waist circumference. In the IDF criterion for adolescents older than 16, reference values developed for adults should be used [36]. Furthermore, recent studies has shown that obese children and adolescents, with higher intra-abdominal fat are more prone to develop MS and non alcoholic fatty liver disease than those with higher values of subcutaneous fat, independent of possible confounding variables. It may be explained by the endocrine function of the adipose tissue (adipokines production), causing inflammatory process and insulin resistance, especially visceral adipose tissue, which has particularities related to higher lipolysis and higher release of adipokines [37]. Among the cited criteria, the most used are that from WHO and that of NCEP-ATP III and some differences among them are observed. The definition from WHO requires evaluation of resistance to insulin or the alteration of the glucose metabolism. On the other hand, the definition from NCEP-ATP III does not require the measuring of resistance to insulin, facilitating its use in epidemiological studies [38]. Comparative studies, using various diagnostic criteria of the metabolic syndrome for children and adolescents confirms the difference in prevalence and verifies that the one connected with WHO was the one which resulted in greater prevalence and consequently the one recommended because of the emphasis on glycemic homeostasis [32,39]. The prevalence of the syndrome in Brazil in children and obese adolescents can reach between 23% [40] to 39.1% [41]. The importance of identifying the risk factors and the forms of control and the treatment of MS in infancy and adolescence is because its presence in this phase of life remains, many years in “silence”. Therefore, its identification can contribute to the prevention of chronic diseases and premature death. Currently, there already exist MS definitions for children and adolescents which use as one of the criteria the abdominal obesity [42,43]. In Table 4 there are presented the main parameters and their respective reference values which are applied to children and adolescents. Some authors also adapted definitions proposed for adults to be applied on children and adolescents (Table 5).
Conclusion The prevalence of MS has increased in the whole world’s adult population and pediatric population, and defining its prevalence has been an arduous task, due to the lack of consensus of its diagnostic criteria. When dealing with the ease in relation to its applicability and sensitivity, the criteria from the International Diabetes Federation can be considered the most advantageous. However, considering the efficacy of the diagnosis, the criteria which most emphasizes the characteristics of glycemic homeostasis, and consequently the main risk factor of MS, resistance to insulin, is the criteria from the World Health Organization for taking into consideration the risk factors like fasting glucose, hyperinsulinemia and glucose intolerance.
References
- James PT, Rigby N, Leach R; International Obesity Task Force (2004) The obesity epidemic, metabolic syndrome and future prevention strategies. Eur J Cardiovasc Prev Rehabil 11: 3-8.
- Adams KF, Schatzkin A, Harris TB, Kipnis V, Mouw T, et al. (2006) Overweight, obesity, and mortality in a large prospective cohort of persons 50 to 71 years old. N Engl J Med 355: 763-778.
- Sinaiko A (2007) Obesity, insulin resistance and the metabolic syndrome. J Pediatr (Rio J) 83: 3-4.
- Aggoun Y (2007) Obesity, metabolic syndrome, and cardiovascular disease. Pediatr Res 61: 653-659.
- Ferreira AP, Oliveira CER, França NM (2007) SÃndrome metabólica em crianças obesas e fatores de risco para doenças cardiovasculares de acordo com a resistência à insulina (HOMA-IR). J Pediatr 83: 21-26
- Huang TT (2008) Finding thresholds of risk for components of the pediatric metabolic syndrome. J Pediatr 152: 158-159.
- Chen W, Berenson GS (2007) Metabolic syndrome: definition and prevalence in children. J Pediatr (Rio J) 83: 1-2.
- Lopes, HF (2004) SÃndrome metabólica: aspectos históricos, prevalência, e morbidade e mortalidade. Rev Soc Cardiol Estado de São Paulo. 4: 539-543.
- Maraton G (1922) Uber hypertonie und Zuckerkrankheit. Z Inn Med. 43: 169-176.
- Nilsson S (2001) [Research contributions of Eskil Kylin]. Sven Med Tidskr 5: 15-28.
- Avogaro P, Crepaldi G, Enzi G, Tiengo A (1965) [Metabolic aspects of essential obesity]. Epatologia 11: 226-238.
- Defronzo RA (1979) Glucose intolerance and aging: evidence for tissue insensitivity to insulin. Diabetes 28: 1095-1101.
- DeFronzo RA, Tobin JD, Andres R (1979) Glucose clamp technique: a method for quantifying insulin secretion and resistance. Am J Physiol 237: E214-223.
- Lottenberg SA, Glezer A, Turatti LA (2007) Metabolic syndrome: identifying the risk factors. J Pediatr (Rio J) 83: S204-208.
- Reaven GM, Hoffman BB (1987) A role for insulin in the aetiology and course of hypertension? Lancet 2: 435-437.
- Reaven GM (1993) Role of insulin resistance in human disease (syndrome X): an expanded definition. Annu Rev Med 44: 121-131.
- Reaven GM, Chen YD (1988) Role of abnormal free fatty acid metabolism in the development of non-insulin-dependent diabetes mellitus. Am J Med 85: 106-112.
- Chen W, Srinivasan SR, Li S, Xu J, Berenson GS (2005) Metabolic syndrome variables at low levels in childhood are beneficially associated with adulthood cardiovascular risk: the Bogalusa Heart Study. Diabetes Care 28: 126-131.
- Franks PW, Hanson RL, Knowler WC, Moffett C, Enos G, et al. (2007) Childhood predictors of young-onset type 2 diabetes. Diabetes 56: 2964-2972.
- Morrison JA, Friedman LA, Gray-McGuire C (2007) Metabolic syndrome in childhood predicts adult cardiovascular disease 25 years later: the Princeton Lipid Research Clinics Follow-up Study. Pediatrics. 120: 340-345.
- Grundy SM (2008) Metabolic syndrome pandemic. Arterioscler Thromb Vasc Biol 28: 629-636.
- Després JP, Lemieux I (2006) Abdominal obesity and metabolic syndrome. Nature 444: 881-887.
- Park YW, Zhu S, Palaniappan L, Heshka S, Carnethon MR, et al. (2003) The metabolic syndrome: prevalence and associated risk factor findings in the US population from the Third National Health and Nutrition Examination Survey, 1988-1994. Arch Intern Med 163: 427-436.
- Cameron AJ, Shaw JE, Zimmet PZ (2004) The metabolic syndrome: prevalence in worldwide populations. Endocrinol Metab Clin North Am 33: 351-375.
- Velásquez-Meléndez G, Gazzinelli A, Côrrea-Oliveira R, Pimenta AM, Kac G (2007) Prevalence of metabolic syndrome in a rural area of Brazil. Sao Paulo Med J 125: 155-162.
- Hu G, Qiao Q, Tuomilehto J, Balkau B, Borch-Johnsen K, et al. (2004) Prevalence of the metabolic syndrome and its relation to all-cause and cardiovascular mortality in nondiabetic European men and women. Arch Intern Med 164: 1066-1076.
- Isomaa B, Almgren P, Tuomi T, Forsén B, Lahti K, et al. (2001) Cardiovascular morbidity and mortality associated with the metabolic syndrome. Diabetes Care 24: 683-689.
- McNeill AM, Rosamond WD, Girman CJ, Golden SH, Schmidt MI, et al. (2005) The metabolic syndrome and 11-year risk of incident cardiovascular disease in the atherosclerosis risk in communities study. Diabetes Care 28: 385-390.
- Sattar N, Gaw A, Scherbakova O, Ford I, O'Reilly DS, et al. (2003) Metabolic syndrome with and without C-reactive protein as a predictor of coronary heart disease and diabetes in the West of Scotland Coronary Prevention Study. Circulation 108: 414-419.
- Skilton MR, Moulin P, Sérusclat A, Nony P, Bonnet F (2007) A comparison of the NCEP-ATPIII, IDF and AHA/NHLBI metabolic syndrome definitions with relation to early carotid atherosclerosis in subjects with hypercholesterolemia or at risk of CVD: evidence for sex-specific differences. Atherosclerosis 190: 416-422.
- Machado UF, Schaan BD, Seraphim PM (2006) [Glucose transporters in the metabolic syndrome]. Arq Bras Endocrinol Metabol 50: 177-189.
- Sangun Ö, Dündar B, Kösker M, Pirgon Ö, Dündar N (2011) Prevalence of metabolic syndrome in obese children and adolescents using three different criteria and evaluation of risk factors. J Clin Res Pediatr Endocrinol 3: 70-76.
- 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 285: 2486e97.
- I Diretriz Brasileira de Diagnóstico e Tratamento da SÃndrome Metabólica. Rev Soc Bras Hipertens 7: 123-162.
- Back Giuliano Ide C, Caramelli B, Pellanda L, Duncan B, Mattos S, et al. (2005) [I guidelines of prevention of atherosclerosis in childhood and adolescence]. Arq Bras Cardiol 85 Suppl 6: 4-36.
- Zimmet P, Alberti KG, Kaufman F, Tajima N, Silink M, et al. (2007) The metabolic syndrome in children and adolescents - an IDF consensus report. Pediatr Diabetes 8: 299-306.
- Silveira LS, Monteiro PA, Antunes Bde M, Seraphim PM, Fernandes RA, et al. (2013) Intra-abdominal fat is related to metabolic syndrome and non-alcoholic fat liver disease in obese youth. BMC Pediatr 13: 115.
- Moraes AC, Fulaz CS, Netto-Oliveira ER, Reichert FF (2009) [Prevalence of metabolic syndrome in adolescents: a systematic review]. Cad Saude Publica 25: 1195-1202.
- Cizmecioğlu FM, Hatun S, Kalaça S (2008) Metabolic syndrome in obese Turkish children and adolescents: comparison of two diagnostic models. Turk J Pediatr 50: 359-365.
- Invitti C, Maffeis C, Gilardini L, Pontiggia B, Mazzilli G, et al. (2006) Metabolic syndrome in obese Caucasian children: prevalence using WHO-derived criteria and association with nontraditional cardiovascular risk factors. Int J Obes (Lond) 30: 627-633.
- Pirkola J, Tammelin T, Bloigu A, Pouta A, Laitinen J, et al. (2008) Prevalence of metabolic syndrome at age 16 using the International Diabetes Federation paediatric definition. Arch Dis Child 93: 945-951.
- Strufaldi MW, Silva EM, Puccini RF (2008) Metabolic syndrome among prepubertal Brazilian schoolchildren. Diab Vasc Dis Res 5: 291-297.
- Teixeira CGO, Silva FM, Verânico PEM (2009) Relação entre obesidade e sÃndrome metabólica em adolescentes de 10 a 14 anos com obesidade abdominal. Acta Scientiarum. Health Science.
- World Health Organization (1999) Definition, diagnosis and classification of diabetes mellitus and its complications: Report of WHO a Consultation. Part 1: diagnosis and classification of diabetes mellitus. Genebra.
- National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents (2004) The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics 114: 555-576.
- Cook S, Weitzman M, Auinger P, Nguyen M, Dietz WH (2003) Prevalence of a metabolic syndrome phenotype in adolescents: findings from the third National Health and Nutrition Examination Survey, 1988-1994. Arch Pediatr Adolesc Med 157: 821-827.
- de Ferranti SD, Gauvreau K, Ludwig DS, Neufeld EJ, Newburger JW, et al. (2004) Prevalence of the metabolic syndrome in American adolescents: findings from the Third National Health and Nutrition Examination Survey. Circulation 110: 2494-2497.
- Cruz ML, Goran MI (2004) The metabolic syndrome in children and adolescents. Curr Diab Rep 4: 53-62.
- Weiss R, Dziura J, Burgert TS, Tamborlane WV, Taksali SE, et al. (2004) Obesity and the metabolic syndrome in children and adolescents. N Engl J Med 350: 2362-2374.
- Ford ES (2005) Prevalence of the metabolic syndrome defined by the International Diabetes Federation among adults in the U.S. Diabetes Care 28: 2745-2749.
Nenhum comentário:
Postar um comentário