Genetic Linkage and Association of the Growth Hormone Secretagogue Receptor (Ghrelin Receptor) Gene in Human Obesity
- 1 January 2005
- journal article
- Published by American Diabetes Association in Diabetes
- Vol. 54 (1) , 259-267
- https://doi.org/10.2337/diabetes.54.1.259
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.Keywords
This publication has 55 references indexed in Scilit:
- RNA regulation: a new genetics?Nature Reviews Genetics, 2004
- Changes in ghrelin and ghrelin receptor expression according to feeding statusNeuroReport, 2003
- Changes in ghrelin and ghrelin receptor expression according to feeding statusNeuroReport, 2003
- Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humansNature Genetics, 2003
- Genetics and Pathophysiology of Human ObesityAnnual Review of Medicine, 2003
- A Combined Analysis of Genomewide Linkage Scans for Body Mass Index, from the National Heart, Lung, and Blood Institute Family Blood Pressure ProgramAmerican Journal of Human Genetics, 2002
- Patterns of linkage disequilibrium in the human genomeNature Reviews Genetics, 2002
- Ghrelin, a Natural GH Secretagogue Produced by the Stomach, Induces Hyperglycemia and Reduces Insulin Secretion in HumansJournal of Clinical Endocrinology & Metabolism, 2001
- The cardiovascular risk factor profile in the study area Augsburg. Results from the first MONICA survey 1984/85Acta Medica Scandinavica, 1988
- The world health organization monica project (monitoring trends and determinants in cardiovascular disease): A major international collaborationJournal of Clinical Epidemiology, 1988