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Diabetes 55:856-861, 2006
DOI: 10.2337/diabetes.55.03.06.db05-0665
© 2006 by the American Diabetes Association
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Brief Genetics Reports

Genetic Analysis of ADIPOR1 and ADIPOR2 Candidate Polymorphisms for Type 2 Diabetes in the Caucasian Population

Martine Vaxillaire1, Aurélie Dechaume1, Valérie Vasseur-Delannoy1, Saida Lahmidi1, Vincent Vatin1, Frédéric Leprêtre1, Philippe Boutin1, Serge Hercberg2, Guillaume Charpentier3, Christian Dina1, and Philippe Froguel1,4

1 Centre National de la Recherche Scientifique (CNRS) UMR 8090, Institute of Biology and Pasteur Institute, Lille, France
2 Scientific and Technical Institute of Nutrition and Food (ISTNA-CNAM), Institut National de la Santé et de la Recherche Médicale (INSERM) U557, INRA U1125, Paris, France
3 Department of Endocrinology and Diabetology, Centre Hospitalier Sud Francilien, Corbeil-Essonnes, France
4 Section of Genomic Medicine, Imperial College Genome Centre, Hammersmith Campus, Imperial College London, London, U.K

Address correspondence and reprint requests to Dr. Martine Vaxillaire, CNRS 8090, Institut de Biologie, Institut Pasteur de Lille, 1 rue du Professeur Calmette, BP 245, 59019 Lille, France. E-mail: martine.vaxillaire{at}pasteur-lille.fr

Abbreviations: AdipoR1, adiponectin receptor 1; AdipoR2, adiponectin receptor 2; HWE, Hardy-Weinberg equilibrium; LD, linkage disequilibrium; MAF, minor allele frequency; SNP, single nucleotide polymorphism; UTR, untranslated region

Adiponectin is a metabolic link between adipose tissue and insulin action, mediating part of obesity-associated insulin resistance and type 2 diabetes. Two adiponectin receptors have been identified, and we investigated whether sequence variations in adiponectin receptor 1 (ADIPOR1) and adiponectin receptor 2 (ADIPOR2) genes could contribute to the genetic risk for type 2 diabetes in a case-control study of 1,498 Caucasian subjects. We sequenced the putative functional regions of the two genes in 48 subjects and selected single nucleotide polymorphisms (SNPs) from the public database. Five SNPs in ADIPOR1 and 12 in ADIPOR2 were tested for association with type 2 diabetes. No SNP of ADIPOR1 showed association in any of the samples from the French population. In contrast, three SNPs of ADIPOR2 showed nominal evidence for association with type 2 diabetes before correction for multiple testing (odds ratio [OR] 1.29–1.37, P = 0.034–0.014); only rs767870, located in intron 6, was replicated in an additional diabetes dataset (n = 636, OR 1.29, P = 0.020) with significant allelic association from the overall meta-analysis of 2,876 subjects (adjusted OR 1.25 [95% CI 1.07–1.45], P = 0.0051). In conclusion, our data suggest a modest contribution of ADIPOR2 variants in diabetes risk in the French population.


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