THE RELEVANCE OF METABOLIC PHENOTYPES OF OBESITY IN CHILDHOOD AND ADOLESCENCE

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Rationale: The study  on  specifics of metabolic phenotypes of obesity in children and adolescents seems be highly relevant for a comprehensive assessment  of causal and  pathophysiological  roles of obesity in the  atherogenesis. Aim: To identify particulars of metabolic  phenotypes of obesity in the  population of the  school children in the  city of Arkhangelsk. Materials and methods: We examined 102 patients aged from 10 to 15 years with obesity, abdominal type (boys, 44.6%, girls, 55.4%). According to the results of a comprehensive clinical and laboratory assessments, the patients  were divided  into  the  group  of metabolically  healthy obese   (children  and  adolescents  with  obesity, but without any metabolic abnormalities) and the group of metabolically unhealthy obese (having at least 1 metabolic abnormality). The list of metabolic abnormalities  included  high triglyceride levels, low levels of high density lipoprotein  cholesterol (HDL-C), high blood pressure, impaired fasting glucose, increased  C-reactive protein  levels. Results: The  group  comparison   showed  that  the  mean levels  of  all studied   parameters  of  pro-atherogenic  metabolic  abnormalities  were significantly higher  in the  patients  with  metabolically  active obesity (the mean triglyceride levels in the groups of metabolically active and metabolically healthy obesity were 1.31 vs 0.74 mmol/L, glucose levels, 4.92  vs 4.54  mmol/L,  C-reactive protein,  3.15  vs 2.30 mg/mL, systolic and diastolic blood pressure, 118.97 vs 110.23 mmHg and 72.90 vs 68.58 mmHg, respectively; p < 0.001), with the  exclusion of the   mean level of anti-atherogenic HDL-C, which was lower (1.27 vs 1.49 mmol/L; p < 0.001). Also, in addition to abdominal obesity, 21.43% of school children with metabolically active obesity had ≥ 2 atherogenic factors, as well as some pro-inflammatory abnormalities (C-reactive protein levels were higher in one third of children and adolescents of this group, with a borderline  significance level). Sixty percent  of children and adolescents with obesity and metabolic abnormalities had abnormal lipid parameters. Pro-atherogenic metabolic abnormalities  were  found  in all children  and  adolescents with increased C-reactive protein levels. Conclusion:  Distinctly different  phenotypes  of obesity with various degrees  of metabolic  abnormalities were  found  in the  pediatric  population. Formation of combination of atherogenic clinical and metabolic abnormalities  (dyslipidemia, impaired glucose  tolerance,  high blood  pressure)  is possible already in children and adolescents with metabolically active obesity. They can be associated with chronic inflammation, and as such could be the first stage of development of atherosclerosis, metabolic  syndrome  and  cardiovascular  disease.

About the authors

S. I. Malyavskaya

Northern State Medical University, Arkhangelsk

Author for correspondence.
Email: malyavskaya@yandex.ru
Malyavskaya Svetlana I. – MD, Professor, Head of Chair of Pediatrics, Prorector for Research Russian Federation

A. V. Lebedev

Northern State Medical University, Arkhangelsk

Email: malyavskaya@yandex.ru
Lebedev Andrey V. – PhD, Associate Professor, Chair of Pathophysiology Russian Federation

References

  1. Bertuccio P, Levi F, Lucchini F, Chatenoud L, Bosetti C, Negri E, La Vecchia C. Coronary heart disease and cerebrovascular disease mortality in young adults: recent trends in Europe. Eur J Cardiovasc Prev Rehabil. 2011;18(4):627–34. doi: 10.1177/1741826710389393.
  2. Кардиоваскулярная профилактика. Национальные рекомендации. Кардиоваскулярная терапия и профилактика. 2011;10(6 Прил 2):1–64.
  3. Zimmet P, Alberti KG, Kaufman F, Tajima N, Silink M, Arslanian S, Wong G, Bennett P, Shaw J, Caprio S; IDF Consensus Group. The metabolic syndrome in children and adolescents – an IDF consensus report. Pediatr Diabetes. 2007;8(5):299–306.
  4. McCrindle BW, Urbina EM, Dennison BA, Jacobson MS, Steinberger J, Rocchini AP, Hayman LL, Daniels SR; American Heart Association Atherosclerosis, Hypertension, and Obesity in Youth Committee; American Heart Association Council of Cardiovascular Disease in the Young; American Heart Association Council on Cardiovascular Nursing. Drug therapy of high-risk lipid abnormalities in children and adolescents: a scientific statement from the American Heart Association Atherosclerosis, Hypertension, and Obesity in Youth Committee, Council of Cardiovascular Disease in the Young, with the Coun cil on Cardiovascular Nursing. Circulation. 2007;115(14):1948–67.
  5. Профилактика сердечно-сосудистых заболеваний в детском и подростковом возрасте. Российские рекомендации. Российский кардиологический журнал. 2012;6(98 Прил 1):1–40.
  6. Hu G, Qiao Q, Tuomilehto J, Balkau B, BorchJohnsen K, Pyorala K; DECODE Study Group. Prevalence of the metabolic syndrome and its relation to all-cause and cardiovascular mortality in nondiabetic European men and women. Arch Intern Med. 2004;164(10):1066–76.
  7. Малявская СИ. Педиатрический метаболический синдром: состояние высокого риска. Педиатрия. 2010;4(89):119–22.
  8. Gami AS, Witt BJ, Howard DE, Erwin PJ, Gami LA, Somers VK, Montori VM. Metabolic syndrome and risk of incident cardiovascular events and death: a systematic review and meta-analysis of longitudinal studies. J Am Coll Cardiol. 2007;49(4):403–14.
  9. Björntorp P. The regulation of adipose tissue distribution in humans. Int J Obes Relat Metab Disord. 1996;20(4):291–302.
  10. Karelis AD, St-Pierre DH, Conus F, Rabasa-Lhoret R, Poehlman ET. Metabolic and bodycomposition factors in subgroups of obesity: what do we know? J Clin Endocrinol Metab. 2004;89(6):2569–75.
  11. Thalmann S, Meier CA. Local adipose tissue depots as cardiovascular risk factors. Cardiovasc Res. 2007;75(4):690–701.
  12. Гусова ЗР, Дзантиева ЕО, Хрипун ИА. Иммунологические аспекты ожирения. Альманах клинической медицины. 2015; Спецвыпуск 1:30–5.
  13. Shaharyar S, Roberson LL, Jamal O, Younus A, Blaha MJ, Ali SS, Zide K, Agatston AA, Blumenthal RS, Conceição RD, Santos RD, Nasir K. Obesity and metabolic phenotypes (metabolically healthy and unhealthy variants) are significantly associated with prevalence of elevated C-reactive protein and hepatic steatosis in a large healthy Brazilian population. J Obes. 2015;2015:178526. doi: 10.1155/2015/178526.
  14. Fantuzzi G. Adipose tissue, adipokines, and inflammation. J Allergy Clin Immunol. 2005;115(5):911–9.
  15. Tchernof A, Després JP. Pathophysiology of human visceral obesity: an update. Physiol Rev. 2013;93(1):359–404. doi: 10.1152/physrev.00033.2011.
  16. Kelley DE, Thaete FL, Troost F, Huwe T, Goodpaster BH. Subdivisions of subcutaneous abdominal adipose tissue and insulin resistance. Am J Physiol Endocrinol Metab. 2000;278(5):E941–8.
  17. Rosen ED, Spiegelman BM. Adipocytes as regulators of energy balance and glu cose homeostasis. Nature. 2006;444(7121): 847–53.
  18. Carey DG. Abdominal obesity. Curr Opin Lipidol. 1998;9(1):35–40.
  19. Sjöström CD, Lissner L, Sjöström L. Relationships between changes in body composition and changes in cardiovascular risk factors: the SOS Intervention Study. Swedish Obese Subjects. Obes Res. 1997;5(6):519–30.
  20. Чумакова ГА, Веселовская НГ, Гриценко ОВ, Отт АВ. Метаболический синдром: сложные и нерешенные проблемы. Российский кардиологический журнал. 2014;3(107):63–71.
  21. Берштейн ЛМ, Коваленко ИГ. «Метаболически здоровые» лица с ожирением и метаболические признаки ожирения у лиц с нормальной массой тела: что за этим стоит? Проблемы эндокринологии. 2010;3:48–51.
  22. Puri R. Is it finally time to dispel the concept of metabolically-healthy obesity? J Am Coll Cardiol. 2014;63(24):2687–8. doi: 10.1016/j. jacc.2014.03.043.
  23. Rosito GA, Massaro JM, Hoffmann U, Ruberg FL, Mahabadi AA, Vasan RS, O'Donnell CJ, Fox CS. Pericardial fat, visceral abdominal fat, cardiovascular disease risk factors, and vascular calcification in a community-based sample: the Framingham Heart Study. Circulation. 2008;117(5):605–13. doi: 10.1161/CIRCULATIONAHA.107.743062.
  24. Hittel DS, Berggren JR, Shearer J, Boyle K, Houmard JA. Increased secretion and expression of myostatin in skeletal muscle from extremely obese women. Diabetes. 2009;58(1):30–8. doi: 10.2337/db08-0943.
  25. Al Suwaidi J. Is there an increased cardiovascular risk in metabolically healthy obese individuals? Lessons from the HUNT (Nord-Trøndelag Health) study. Glob Cardiol Sci Pract. 2014;2014(2):44–7. doi: 10.5339/gcsp.2014.24.
  26. Романцова ТИ, Островская ЕВ. Метаболически здоровое ожирение: дефиниции, протективные факторы, клиническая значимость. Альманах клинической медицины. 2015; Спецвыпуск 1:75–86.
  27. Stefan N, Schick F, Häring HU. Ectopic fat in insulin resistance, dyslipidemia, and cardiometabolic disease. N Engl J Med. 2014;371(23):2236– 7. doi: 10.1056/NEJMc1412427#SA3.
  28. Cole TJ, Bellizzi MC, Flegal KM, Dietz WH. Establishing a standard definition for childoverweight and obesityworldwide: international survey. BMJ. 2000;320(7244):1240–3.

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Copyright (c) 2015 Malyavskaya S.I., Lebedev A.V.

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