4.6 Article

Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals

期刊

ATHEROSCLEROSIS
卷 208, 期 2, 页码 412-420

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2009.11.035

关键词

Adiponectin; Genome-wide association study; Polymorphism; Cardiovascular disease; Metabolic syndrome

资金

  1. Medical Research Council [G9815508, G0600705, G0800582] Funding Source: Medline
  2. NHLBI NIH HHS [N01 HC025195] Funding Source: Medline
  3. NIDDK NIH HHS [R01 DK075787, R01 DK075787-01A1] Funding Source: Medline
  4. Medical Research Council [G0800582, G0600705, G9815508] Funding Source: researchfish
  5. MRC [G0600705, G0800582] Funding Source: UKRI

向作者/读者索取更多资源

Objective: Plasma adiponectin is strongly associated with various components of metabolic syndrome, type 2 diabetes and cardiovascular outcomes. Concentrations are highly heritable and differ between men and women. We therefore aimed to investigate the genetics of plasma adiponectin in men and women. Methods: Wecombined genome-wide association scans of three population-based studies including 4659 persons. For the replication stage in 13795 subjects, we selected the 20 top signals of the combined analysis, as well as the 10 top signals with p-values less than 1.0 x 10(-4) for each the men-and the women-specific analyses. We further selected 73 SNPs that were consistently associated with metabolic syndrome parameters in previous genome-wide association studies to check for their association with plasma adiponectin. Results: The ADIPOQ locus showed genome-wide significant p-values in the combined (p = 4.3 x 10(-24)) as well as in both women-and men-specific analyses (p = 8.7 x 10(-17) and p = 2.5 x 10(-11), respectively). None of the other 39 top signal SNPs showed evidence for association in the replication analysis. None of 73 SNPs from metabolic syndrome loci e x hibited association with plasma adiponectin (p > 0.01). Conclusions: We demonstrated the ADIPOQ gene as the only major gene for plasma adiponectin, which e x plains 6.7% of the phenotypic variance. We further found that neither this gene nor any of the metabolic syndrome loci e x plained the se x differences observed for plasma adiponectin. Larger studies are needed to identify more moderate genetic determinants of plasma adiponectin. (C) 2009 Elsevier Ireland Ltd. All rights reserved.

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