ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity
- Nabila Bouatia-Naji1,
- David Meyre1,
- Stéphane Lobbens1,
- Karin Séron1,
- Frédéric Fumeron2,
- Beverley Balkau3,
- Barbara Heude3,
- Béatrice Jouret4,
- Philipp E. Scherer5,
- Christian Dina1,
- Jacques Weill6 and
- Philippe Froguel17
- 1Centre National de la Recherche Scientifique UMR8090, Pasteur Institute of Lille, Lille, France
- 2Institut National de la Santé et de la Recherche Médicale (INSERM) U695, Faculty of Medicine Xavier Bichat, Paris, France
- 3INSERM, U258-IFR69, Faculty of Medicine Paris Sud, Villejuif, France
- 4INSERM U563, Children’s Hospital, Toulouse, France
- 5Department of Cell Biology and Diabetes Research and Training Centre, Albert Einstein College of Medicine, Bronx, New York
- 6Pediatric Endocrine Unit, Jeanne de Flandre Hospital, Lille, France
- 7Genomic Medicine and Genome Centre, Hammersmith Campus, Imperial College, London, U.K
- Address correspondence and reprint requests to Philippe Froguel, Genomic Medicine, Imperial College London, Hammersmith Hospital, Du Cane Road, London, W12 0NN, U.K. E-mail: p.froguel{at}imperial.ac.uk
Abstract
Common single nucleotide polymorphisms (SNPs) in the ACDC adiponectin encoding gene have been associated with insulin resistance and type 2 diabetes in several populations. Here, we investigate the role of SNPs −11,377C>G, −11,391G>A, +45T>G, and +276G>T in 2,579 French Caucasians (1,229 morbidly obese and 1,350 control subjects). We found an association between severe forms of obesity and −11,377C (odds ratio 1.23, P = 0.001) and +276T (1.19, P = 0.006). Surprisingly, alternative alleles −11,377G and +276G have been previously reported as risk factors for type 2 diabetes. Transmission disequilibrium tests showed a trend in overtransmission (56.7%) of a risk haplotype 1(C)-1(G)-1(T)-2(T) including −11,377C and +276T in 634 obesity trios (P = 0.097). Family-based analysis in 400 trios from the general population indicated association between obesity haplotype and higher adiponectin levels, suggesting a role of hyperadiponectinemia in weight gain. However, experiments studying the putative roles of SNPs −11,377C>G and +276G>T on ACDC functionality were not conclusive. In contrast, promoter SNP −11,391G>A was associated with higher adiponectin levels in obese children (P = 0.005) and in children from the general population (0.00007). In vitro transcriptional assays showed that −11,391A may increase ACDC activity. In summary, our study suggests that variations at the ACDC/adiponectin gene are associated with risk of severe forms of obesity. However, the mechanisms underlying these possible associations are not fully understood.
- EMSA, electrophoretic mobility shift assay
- FLVS, Fleurbaix-Laventie Ville Santé
- SNP, single nucleotide polymorphism
- TDT, transmission disequilibrium test
Footnotes
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Additional information on this brief genetics report can be found in an online appendix available from http://diabetes.diabetesjournals.org.
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- Accepted October 19, 2005.
- Received July 29, 2005.
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