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

IM Heid, Peter Henneman, A Hicks, S Coassin, T Winkler, YS Aulchenko, C Fuchsberger, K Song, MF Hivert, DM Waterworth, NJ Timpson, JB Richards, JRB Perry, T Tanaka, Najaf Amin, B Kollerits, I Pichler, Ben Oostra, B Thorand, RR FrantsT Illig, J Dupuis, B Glaser, T Spector, J Guralnik, JM Egan, JC Florez, DM Evans, N Soranzo, S Bandinelli, OD Carlson, TM Frayling, K Burling, GD Smith, V Mooser, L Ferrucci, JB Meigs, P Vollenweider, KW van Dijk, P Pramstaller, F Kronenberg, Cornelia Duijn

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Abstract

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.
Original languageUndefined/Unknown
Pages (from-to)412-420
Number of pages9
JournalAtherosclerosis
Volume208
Issue number2
DOIs
Publication statusPublished - 2010

Research programs

  • EMC MGC-02-96-01
  • EMC NIHES-01-64-02

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