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Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
Authors:Dastani Zari  Hivert Marie-France  Timpson Nicholas  Perry John R B  Yuan Xin  Scott Robert A  Henneman Peter  Heid Iris M  Kizer Jorge R  Lyytikäinen Leo-Pekka  Fuchsberger Christian  Tanaka Toshiko  Morris Andrew P  Small Kerrin  Isaacs Aaron  Beekman Marian  Coassin Stefan  Lohman Kurt  Qi Lu  Kanoni Stavroula  Pankow James S  Uh Hae-Won  Wu Ying  Bidulescu Aurelian  Rasmussen-Torvik Laura J  Greenwood Celia M T  Ladouceur Martin  Grimsby Jonna  Manning Alisa K  Liu Ching-Ti  Kooner Jaspal  Mooser Vincent E  Vollenweider Peter  Kapur Karen A  Chambers John  Wareham Nicholas J  Langenberg Claudia  Frants Rune
Affiliation:Department of Epidemiology, Biostatistics, and Occupational Health, Jewish General Hospital, Lady Davis Institute, McGill University, Montreal, Canada.
Abstract:Circulating levels of adiponectin, a hormone produced predominantly by adipocytes, are highly heritable and are inversely associated with type 2 diabetes mellitus (T2D) and other metabolic traits. We conducted a meta-analysis of genome-wide association studies in 39,883 individuals of European ancestry to identify genes associated with metabolic disease. We identified 8 novel loci associated with adiponectin levels and confirmed 2 previously reported loci (P = 4.5×10−8–1.2×10−43). Using a novel method to combine data across ethnicities (N = 4,232 African Americans, N = 1,776 Asians, and N = 29,347 Europeans), we identified two additional novel loci. Expression analyses of 436 human adipocyte samples revealed that mRNA levels of 18 genes at candidate regions were associated with adiponectin concentrations after accounting for multiple testing (p<3×10−4). We next developed a multi-SNP genotypic risk score to test the association of adiponectin decreasing risk alleles on metabolic traits and diseases using consortia-level meta-analytic data. This risk score was associated with increased risk of T2D (p = 4.3×10−3, n = 22,044), increased triglycerides (p = 2.6×10−14, n = 93,440), increased waist-to-hip ratio (p = 1.8×10−5, n = 77,167), increased glucose two hours post oral glucose tolerance testing (p = 4.4×10−3, n = 15,234), increased fasting insulin (p = 0.015, n = 48,238), but with lower in HDL-cholesterol concentrations (p = 4.5×10−13, n = 96,748) and decreased BMI (p = 1.4×10−4, n = 121,335). These findings identify novel genetic determinants of adiponectin levels, which, taken together, influence risk of T2D and markers of insulin resistance.
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