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 familybased 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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Univ London St Bartholomews Hosp Med Coll, Dept Endocrinol, London EC1A 7BE, EnglandUniv London St Bartholomews Hosp Med Coll, Dept Endocrinol, London EC1A 7BE, England
Korbonits, M
Ciccarelli, E
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机构:Univ London St Bartholomews Hosp Med Coll, Dept Endocrinol, London EC1A 7BE, England
Ciccarelli, E
Ghigo, E
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机构:Univ London St Bartholomews Hosp Med Coll, Dept Endocrinol, London EC1A 7BE, England
Ghigo, E
Grossman, AB
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机构:Univ London St Bartholomews Hosp Med Coll, Dept Endocrinol, London EC1A 7BE, England
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Western Univ, Pathol & Lab Med, London, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Sullivan, Rebecca
Randhawa, Varinder K.
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Univ Hlth Network, Toronto Gen Hosp, Div Cardiol, Toronto, ON, Canada
Univ Toronto, Toronto, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Randhawa, Varinder K.
Lalonde, Tyler
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Western Univ, Chem, London, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Lalonde, Tyler
Yu, Tina
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Western Univ, Med Biophys, London, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Yu, Tina
Kiaii, Bob
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Western Univ, Cardiac Surg, London, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Kiaii, Bob
Luyt, Leonard
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Western Univ, Chem, London, ON, Canada
Western Univ, London Reg Canc Program, Oncol, London, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Luyt, Leonard
Wisenberg, Gerald
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Western Univ, Med Biophys, London, ON, Canada
Lawson Hlth Res Inst, Imaging Program, London, ON, Canada
Lawson Hlth Res Inst, Cardiac Imaging Res, London, ON, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada
Wisenberg, Gerald
Dhanvantari, Savita
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Western Univ, Pathol & Lab Med, London, ON, Canada
Western Univ, Med Biophys, London, ON, Canada
Lawson Hlth Res Inst, Imaging Program, London, ON, Canada
Lawson Hlth Res Inst, Metab & Diabet, London, ON, Canada
Lawson Hlth Res Inst, POB 5777,Stn B, London, ON N6A 4V2, CanadaWestern Univ, Pathol & Lab Med, London, ON, Canada