Serum Asymmetric Dimethylarginine, and Adiponectin as Predictors of Atherosclerotic Risk among Obese Egyptian Children

Authors

  • Enas R. Abdel Hameed Child Health Department, National Research Center, Cairo
  • Inas R. El-Alameey Child Health Department, National Research Center, Cairo
  • Lobna S. Sherif Child Health Department, National Research Center, Cairo
  • Sahar A. Khairy Pediatric Department, National Nutrition Institute, National Research Center, Cairo
  • Amr S. Megawer Pediatric Department, Research Institute of Ophthalmology, National Research Center, Cairo
  • Eman R. Youness Medical Biochemistry Department, Medical Division, National Research Center, Cairo
  • Aisha Mohamed El-Shiemy Clinical Pathology, National Institute of Urology and Nephrology, National Research Center, Cairo

DOI:

https://doi.org/10.3889/oamjms.2014.032

Keywords:

children, obese, Asymmetric Dimethylarginine (ADMA), adiponectin, atherosclerotic risk.

Abstract

BACKGROUND: Obesity is associated with an increased risk of developing hyperinsulinemia, dyslipidemia, hypertension, premature atherosclerosis, and coronary artery disease in the future.

AIM: This study is designed to assess the relationship between serum adiponectin, asymmetric dimethylarginine (ADMA), and lipid profile among Egyptian overweight and obese children.

METHODS: This cross sectional case control study included 40 selected pre-pubertal overweight and obese children, 24 girls (60%) and 16 boys (40%) aged between 5 to 13 years (8.85 ± 2.7 years), from new cases attending the National nutrition institute clinic during 2013. Forty apparently healthy children of matched age and sex were recruited as a control group.

RESULTS: Obese group showed highly significant higher levels of serum ADMA, triglycerides, and total cholesterol compared with healthy controls (P <0.000 in all). However, serum adiponectin levels were highly significant lower in obese children compared to healthy controls (P < 0.000). Serum ADMA showed significant positive correlations with height, serum total cholesterol and serum triglycerides levels and significant negative correlation with the body mass index and weight for age z score.  Serum adiponectin showed significant negative correlations with BMI, weight, and weight for age z score and significant positive correlation with serum triglycerides. By linear regression analysis; serum adiponectin, and serum triglycerides levels were significant predictors of high serum ADMA level (p =0.045 and 0.015 respectively). BMI, weight, height and serum triglycerides were significant predictors of low serum adiponectin levels (p = 0.005, 0.022, 0.026 and 0.015 respectively).

CONCLUSIONS: Our results revealed that ADMA, Adiponectin and lipid profile can be considered as predictive biomarkers in prediction and prevention of atherosclerotic risk in the future among overweight and obese Egyptian children.

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References

Ogden CL, Yanovski SZ, Carroll MD, Flegal KM. The epidemiology of obesity. Gastroenterology. 2007; 132: 2087-2102. DOI: https://doi.org/10.1053/j.gastro.2007.03.052

Biro FM, Wien M. Childhood obesity and adult morbidities. Am J Clin Nutr. 2010; 91:1499–1505. DOI: https://doi.org/10.3945/ajcn.2010.28701B

Lobstein T, Baur L, Uauy R. Obesity in children and young people: a crisis in public health. Obes Rev Suppl. 2004; 5: 4–104. DOI: https://doi.org/10.1111/j.1467-789X.2004.00133.x

Hamdy O, Ledbury S, Mullooly C. Lifestyle modification improves endothelial function in obese subjects with the insulin resistance syndrome. Diabetes Care. 2003; 26: 2119–25. DOI: https://doi.org/10.2337/diacare.26.7.2119

Díez JJ, Iglesias P. The role of the adipocyte-derived hormone adiponectin in human disease. Eur J Endocrinol. 2003; 148 (3): 293–300. DOI: https://doi.org/10.1530/eje.0.1480293

Adamska, AN, Kowalska IM, Otiose E, Górska M, Strączkowski M. Relationships between serum adiponectin and soluble TNF-a receptors and glucose and lipid oxidation in lean and obese subjects. Acta Diabetologica. 2012; 49(1):17-27. DOI: https://doi.org/10.1007/s00592-010-0252-y

Hara K, Yamauchi T, Kadowaki T. Adiponectin: an adipokine linking adipocytes and type 2 diabetes in humans. Curr Diab Rep. 2005;5(2):136-40. DOI: https://doi.org/10.1007/s11892-005-0041-0

Ukkola O, Santaniemi M. Adiponectin as link between excess adiposity and associated comorbidities? J Mol Med. 2005; 80 (11): 696–702. DOI: https://doi.org/10.1007/s00109-002-0378-7

Bonetti PO, Lerman LO, Lerman A. Endothelial dysfunction: a marker of atherosclerotic risk, Arteriosclerosis, Thrombosis, and Vascular Biology. 2003; 23(2): 168–175. DOI: https://doi.org/10.1161/01.ATV.0000051384.43104.FC

Gennaro CV, Bianchi M, Pascale V. Asymmetric dimethylarginine (ADMA): an endogenous inhibitor of nitric oxide synthase and a novel cardiovascular risk molecule. Med Sci Monit. 2009; 15(4): 91–101.

Cooke JP. Does ADMA cause endothelial dysfunction? Arterioscler Thromb Vasc Biol. 2004; 20: 2032-2037. DOI: https://doi.org/10.1161/01.ATV.20.9.2032

Gruber HJ, Mayer C, Meinitzer A. Asymmetric dimethylarginine (ADMA) is tightly correlated with growth in juveniles without correlations to obesity related disorders. Exp Clin Endocrinol Diabetes. 2008; 116: 520–24. DOI: https://doi.org/10.1055/s-2008-1062712

World Health Organization, Expert Committee: Physical status: The use and interpretation of anthropometry. In WHO technical report series 854. Geneva: Report of a WHO Expert Committee, 1995.

Tanner JM, Miernaux J, Jarman S, Weiner JS, Lourie JA. Growth, and physique studies. Human biology, Oxford Blackwell Scientific Publications, 1969:273-275.

Nijveldt, RJ, Teerlink TB, Van der Hoven MP, Siroen DJ, Kuik JA, Rauwerda PA. Asymmetrical dimethylarginine (ADMA) in critically ill patients: high plasma ADMA concentration is an independent risk factor of ICU mortality. Clin Nutr. 2003;22: 23-30. DOI: https://doi.org/10.1054/clnu.2002.0613

Fassati P, Prencipe L. Serum triglycerides determined colorimetrically with an enzyme that produces hydrogen peroxide. Clin Chem. 1982; 28: 2077-2080. DOI: https://doi.org/10.1093/clinchem/28.10.2077

Richmond W. Preparation and properties of a cholesterol oxidase from Nocrdia spand its application to the enzymatic assay of cholesterol in serum. Clin Chem. 1973; 19: 1350-1356. DOI: https://doi.org/10.1093/clinchem/19.12.1350

Bonvecchio A, Safdie M, Monterrubio EA, Gust T, Villalpando S, Rivera JA. Overweight and obesity trends in Mexican children 2 to 18 years of age from 1988 to 2006. Salud Pub Mex. 2009; 51(Suppl 4):S586–S594. DOI: https://doi.org/10.1590/S0036-36342009001000013

Codrington C, Sarri K, Kafatos A. Stakeholder appraisal of policy options for tackling obesity in Greece. Obes Rev. 2007; 8 (Suppl 2):63–73. DOI: https://doi.org/10.1111/j.1467-789X.2007.00360.x

Hassan NE, EL-Ashry HH, Awad AH, El-Masry SA, Youssef M M, Sallam M M, Anwar M. Adiponectin in obese children and its association with blood pressure and anthropometric markers. Medical Research Journal. 2011; 10 (1): 1–4. DOI: https://doi.org/10.1097/01.MJX.0000397204.63056.f3

El Derwi D, El Sherbiny N, Atta AH. Exploring Fayoum (Upper Egypt) preparatory school students’ and teachers’ attitude towards obesity as health risk. J Public Health Epidemiol. 2011; 3: 401– 406.

Shaheen FM, Hathout M, Tawfik AA. National survey of obesity in Egypt. Cairo: Egypt National Nutrition Institute, 2004.

Fatih K, Mehmet T, Sami E, Coskun K, Unlu A, Turgut K, Akif V, Kenan D, Selim A. Serum asymmetric dimethylarginine levels in normotensive obese individuals. Med Sci Monit. 2010; 16(11): 536-539.

Teplan V, Schuck O, Racek J. Asymmetric dimethylarginine in obesity after renal transplantation. J Ren Nutr. 2008; 18: 513–20. DOI: https://doi.org/10.1053/j.jrn.2008.05.005

Kanazawa S, Notsu Y, Yamaguchi H, Nabika T, Sugimoto T. Asymmetric dimethylarginine as a risk factor for cardiovascular disease in Japanese patients with type 2 diabetes mellitus. Clinical Endocrinology. 2011; 74(4): 467–472. DOI: https://doi.org/10.1111/j.1365-2265.2010.03946.x

Boger RH, Maas R, Schulze F, Schwedhelm E. Elevated levels of asymmetric dimethylarginine as a marker for cardiovascular disease and mortality. Clinical Chemistry and Laboratory Medicine. 2005;43(10):1124–1129. DOI: https://doi.org/10.1515/CCLM.2005.196

Sahinarslan A, Cengel A, Biberoglu G, Hasanoglu A, Turkoglu S, Timurkaynak T. Plasma asymmetric dimethylarginine level and extent of lesion at coronary angiography. Coron Artery Dis. 2006; 17: 605-609. DOI: https://doi.org/10.1097/01.mca.0000236282.81985.e2

Hasanoğlu A, Okur I, Oren AC, Biberoğlu G, Oktar S, Eminoğlu FT, Tümer L. The levels of asymmetric dimethylarginine, homocysteine and carotid intima-media thickness in hypercholesterolemic children. Turk J Pediatr. 2011;53(5):522-7.

Su SC, Pei D, Hsieh CH, Hsiao FC, Wu CZ, Hung YJ. Circulating pro-inflammatory cytokines and adiponectin in young men with type 2 diabetes. Acta Diabetol. 2011;48(2):113-9. DOI: https://doi.org/10.1007/s00592-009-0171-y

Weyer C, Funahashi T, Tanaka S, Hotta K, Matsuzawa Y, Pratley RE. Hypoadiponectinemia in obesity and type 2 diabetes: close association with insulin resistance and hyperinsulinemia. J Clin Endocrinol Metab. 2001; 86: 1930–1935. DOI: https://doi.org/10.1210/jcem.86.5.7463

Wagner A, Simon C, Oujaa M, Platat C, Schweitzer B, Arveiler D. Adiponectin is associated with lipid profile and insulin sensitivity in French adolescents. Diabetes Metab. 2008; 34: 465–471. DOI: https://doi.org/10.1016/j.diabet.2008.02.006

Ducluzeau PH, Cousin P, Malvoisin E, Bornet H, Vidal H, Laville M. Glucose-to-insulin ratio rather than sex hormone-binding globulin and adiponectin levels is the best predictor of insulin resistance in nonobese women with polycystic ovary syndrome. J Clin Endocrinol Metab. 2003; 88: 3626–3631. DOI: https://doi.org/10.1210/jc.2003-030219

Klünder M, Flores-Huerta S, García-Macedo R, Jesús PR, Miguel CZ. Adiponectin in eutrophic and obese children as a biomarker to predict metabolic syndrome and each of its components. BMC Public Health. 2013; 13:88-96. DOI: https://doi.org/10.1186/1471-2458-13-88

Arnaiz P, Acevedo M, Barja S, Aglony M, Guzmán B, Cassis B. Adiponectin levels, cardiometabolic risk factors and markers of subclinical atherosclerosis in children. Int J Cardiol. 2010; 138: 138–144. DOI: https://doi.org/10.1016/j.ijcard.2008.08.007

Schoppen S, Riestra P, García-Anguita A, López-Simón L, Cano B, de Oya I. Leptin and adiponectin levels in pubertal children: relationship with anthropometric variables and body composition. Clin Chem Lab Med. 2010; 48: 707–711. DOI: https://doi.org/10.1515/CCLM.2010.142

Ogawa Y, Kikuchi T, Nagasaki K, Hiura M, Tanaka Y, Uchiyama M. Usefulness of Serum Adiponectin Level as a Diagnostic Marker of Metabolic Syndrome in Obese Japanese Children. Hypertension Research. 2005; 28: 51–57. DOI: https://doi.org/10.1291/hypres.28.51

Asayama K, Hayashibe H, Dobashi K, Uchida N, Nakane T, Kodera K. Decrease in serum adiponectin level due to obesity and visceral fat accumulation in children. Obes Res. 2003; 11: 072–1079. DOI: https://doi.org/10.1038/oby.2003.147

Cambuli VM, Musiu MC, Incani M, Paderi M, Serpe R, Marras V. Assessment of adiponectin and leptin as biomarkers of positive metabolic outcomes after lifestyle intervention in overweight and obese children. J Clin Endocrinol Metab. 2008; 93: 3051–3057. DOI: https://doi.org/10.1210/jc.2008-0476

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Published

2014-05-16

How to Cite

1.
Abdel Hameed ER, El-Alameey IR, Sherif LS, Khairy SA, Megawer AS, Youness ER, El-Shiemy AM. Serum Asymmetric Dimethylarginine, and Adiponectin as Predictors of Atherosclerotic Risk among Obese Egyptian Children. Open Access Maced J Med Sci [Internet]. 2014 May 16 [cited 2024 Apr. 19];2(2):209-14. Available from: https://oamjms.eu/index.php/mjms/article/view/oamjms.2014.032

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Section

A - Basic Science

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