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Adipocytokine profile of type 2 diabetics in metabolic syndrome as defined by various criteria.

Authors :
Al-Daghri NM
Al-Attas OS
Al-Rubeaan K
Sallam R
Source :
Diabetes/metabolism research and reviews [Diabetes Metab Res Rev] 2008 Jan-Feb; Vol. 24 (1), pp. 52-8.
Publication Year :
2008

Abstract

Background: This study aims to identify which among the metabolic syndrome (MS) definitions are closely associated with pathological levels of leptin, adiponectin, resistin, tumour necrosis alpha (TNF-alpha) and C-reactive protein (CRP) among type 2 diabetics.<br />Materials and Methods: Three hundred and five (160 males; 145 females) adult type 2 diabetic Saudis participated in this cross-sectional study. Leptin, adiponectin, resistin, TNF-alpha and CRP were analysed, using enzyme-linked immunosorbent assays (ELISA). Each participant was screened for MS based on the definitions of WHO, AHA/NHLBI and IDF.<br />Results: IDF holds the most identified patients [190 (62.3%)] in both, males [107 (66.9%)], and females [83 (57.2%)]. In males, hyperleptinemia, hypoadiponectinemia and hyperresistinemia were strongest in the AHA/NHLBI-defined MS [odds ratio (95% confidence interval 'CI') of 2.03 (1.05-3.93); 1.31 (0.55-3.1); 1.63 (0.42-6.4) respectively]. The risk of elevated CRP was highest on the WHO definition [odds ratio (95% CI) of 2.04 (0.46-9.04)]. In females, the IDF-defined MS has the strongest association in all four parameters: odds ratio (95% CI), as follows: leptin [2.09 (0.14-30.71)]; adiponectin [6.00 (0.47-76.17)]; resistin [0.47 (0.18-1.23)] and CRP [3.07 (0.21-45.10)].<br />Conclusion: Gender differences exist in assessing the risk of various adipocytokine abnormalities in relation to the various criteria. This study supports the use of IDF definition among females and AHA/NHLBI in males in studies involving MS and obesity, since these definitions hold stronger predicting powers in detecting pathological levels of key adipocytokines.<br /> (2007 John Wiley & Sons, Ltd)

Details

Language :
English
ISSN :
1520-7552
Volume :
24
Issue :
1
Database :
MEDLINE
Journal :
Diabetes/metabolism research and reviews
Publication Type :
Academic Journal
Accession number :
17657721
Full Text :
https://doi.org/10.1002/dmrr.763