Literature DB >> 15616037

Genetic linkage and association of the growth hormone secretagogue receptor (ghrelin receptor) gene in human obesity.

Andrea Baessler1, Michael J Hasinoff, Marcus Fischer, Wibke Reinhard, Gabriele E Sonnenberg, Michael Olivier, Jeanette Erdmann, Heribert Schunkert, Angela Doering, Howard J Jacob, Anthony G Comuzzie, Ahmed H Kissebah, Anne E Kwitek.   

Abstract

The growth hormone secretagogue receptor (GHSR) (ghrelin receptor) plays an important role in the regulation of food intake and energy homeostasis. The GHSR gene lies on human chromosome 3q26 within a quantitative trait locus strongly linked to multiple phenotypes related to obesity and the metabolic syndrome. Because the biological function and location of the GHSR gene make it an excellent candidate gene, we tested the relation between common single nucleotide polymorphisms (SNPs) in the GHSR gene and human obesity. We performed a comprehensive analysis of SNPs, linkage disequilibrium (LD), and haplotype structure across the entire GHSR gene region (99.3 kb) in 178 pedigrees with multiple obese members (DNA of 1,095 Caucasians) and in an independent sample of the general population (MONICA Augsburg left ventricular hypertrophy substudy; DNA of 1,418 Caucasians). The LD analysis revealed a disequilibrium block consisting of five SNPs, consistent in both study cohorts. We found linkage among all five SNPs, their haplotypes, and BMI. Further, we found suggestive evidence for transmission disequilibrium for the minor SNP alleles (P < 0.05) and the two most common haplotypes with the obesity affection status ("susceptible" P = 0.025, "nonsusceptible" P = 0.045) in the family cohort using the family-based association test program. Replication of these findings in the general population resulted in stronger evidence for an association of the SNPs (best P = 0.00001) and haplotypes with the disease ("susceptible" P = 0.002, "nonsusceptible" P = 0.002). To our knowledge, these data are the first to demonstrate linkage and association of SNPs and haplotypes within the GHSR gene region and human obesity. This linkage, together with significant transmission disequilibrium in families and replication of this association in an independent population, provides evidence that common SNPs and haplotypes within the GHSR region are involved in the pathogenesis of human obesity.

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Year:  2005        PMID: 15616037      PMCID: PMC2793077          DOI: 10.2337/diabetes.54.1.259

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  50 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

2.  A general test of association for quantitative traits in nuclear families.

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4.  Family-based tests of association in the presence of linkage.

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5.  Ghrelin induces adiposity in rodents.

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3.  Associations of polymorphism within the GHSR gene with growth traits in Nanyang cattle.

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Review 5.  Constitutive activation of G protein-coupled receptors and diseases: insights into mechanisms of activation and therapeutics.

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7.  Association of SNPs in GHSR rs292216 and rs509035 on dietary intake in Indonesian obese female adolescents.

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8.  Molecular characterization of the ghrelin and ghrelin receptor genes and effects on fat deposition in chicken and duck.

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9.  Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity.

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Review 10.  Pediatric obesity: parallels with addiction and treatment recommendations.

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