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J Nutr Metab. 2012;2012:253428. doi: 10.1155/2012/253428. Epub 2011 Aug 22.

Adipokines as possible new predictors of cardiovascular diseases: a case control study.

Journal of nutrition and metabolism

Laura Pala, Matteo Monami, Silvia Ciani, Ilaria Dicembrini, Alessandro Pasqua, Anna Pezzatini, Paolo Francesconi, Barbara Cresci, Edoardo Mannucci, Carlo Maria Rotella

Affiliations

  1. SOD of Endocrinology, AOUC, 50139 Florence, Italy.

PMID: 21869928 PMCID: PMC3160046 DOI: 10.1155/2012/253428

Abstract

Background and Aims. The secretion of several adipocytokines, such as adiponectin, retinol-binding protein 4 (RBP4), adipocyte fatty acid binding protein (aFABP), and visfatin, is altered in subjects with abdominal adiposity; these endocrine alterations could contribute to increased cardiovascular risk. The aim of the study was to assess the relationship among adiponectin, RBP4, aFABP, and visfatin, and incident cardiovascular disease. Methods and Results. A case-control study, nested within a prospective cohort, on 2945 subjects enrolled for a diabetes screening program was performed. We studied 18 patients with incident fatal or nonfatal IHD (Ischemic Heart Disease) or CVD (Cerebrovascular Disease), compared with 18 matched control subjects. Circulating adiponectin levels were significantly lower in cases of IHD with respect to controls. Circulating RBP4 levels were significantly increased in CVD and decreased in IHD with respect to controls. Circulating aFABP4 levels were significantly increased in CVD, while no difference was associated with IHD. Circulating visfatin levels were significantly lower in cases of both CVD and IHD with respect to controls, while no difference was associated with CVD. Conclusions. The present study confirms that low adiponectin is associated with increased incidents of IHD, but not CVD, and suggests, for the first time, a major effect of visfatin, aFABP, and RBP4 in the development of cardiovascular disease.

References

  1. J Clin Endocrinol Metab. 2007 Jul;92(7):2590-7 - PubMed
  2. Heart. 2003 Jun;89(6):667 - PubMed
  3. Heart. 2004 May;90(5):528-33 - PubMed
  4. Atherosclerosis. 2009 Sep;206(1):239-44 - PubMed
  5. Diabetes Res Clin Pract. 2008 Apr;80(1):e13-5 - PubMed
  6. J Clin Endocrinol Metab. 2007 Jul;92(7):2712-9 - PubMed
  7. J Cell Mol Med. 2008 Aug;12(4):1395-403 - PubMed
  8. FASEB J. 2009 Nov;23(11):3865-73 - PubMed
  9. Diabetes. 2006 Oct;55(10):2805-10 - PubMed
  10. N Engl J Med. 2006 Jun 15;354(24):2552-63 - PubMed
  11. Metabolism. 2004 Mar;53(3):303-9 - PubMed
  12. Diabetes Care. 2007 Aug;30(8):e91; author reply e92 - PubMed
  13. Diabetologia. 2007 Sep;50(9):1930-1937 - PubMed
  14. J Clin Endocrinol Metab. 2002 Jun;87(6):2764-9 - PubMed
  15. Metabolism. 2010 Apr;59(4):527-32 - PubMed
  16. Biochem Biophys Res Commun. 1999 Apr 2;257(1):79-83 - PubMed
  17. JAMA. 2004 Apr 14;291(14):1730-7 - PubMed
  18. J Clin Endocrinol Metab. 2007 Nov;92(11):4306-12 - PubMed
  19. Physiol Res. 2008;57(6):927-934 - PubMed
  20. Nature. 2005 Jul 21;436(7049):356-62 - PubMed
  21. Acta Diabetol. 2003 Dec;40(4):181-6 - PubMed
  22. J Clin Endocrinol Metab. 2007 Dec;92(12):4827-34 - PubMed
  23. Lancet. 2005 Nov 5;366(9497):1640-9 - PubMed
  24. JAMA. 2001 May 16;285(19):2486-97 - PubMed
  25. J Clin Endocrinol Metab. 2006 Aug;91(8):3165-70 - PubMed
  26. Diabet Med. 2006 May;23(5):469-80 - PubMed
  27. Clin Exp Hypertens. 1999 Jul-Aug;21(5-6):1009-60 - PubMed
  28. Diabetes Care. 2006 Nov;29(11):2457-61 - PubMed
  29. Arterioscler Thromb Vasc Biol. 2005 Apr;25(4):821-6 - PubMed

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