Ghrelin receptor gene polymorphisms and body size in children and adults

被引:21
作者
Garcia, Edwin A. [1 ]
Heude, Barbara [2 ,4 ,5 ]
Petry, Clive J. [3 ]
Gueorguiev, Maria [1 ]
Hassan-Smith, Zaki K. [1 ]
Spanou, Antigoni [1 ]
Ring, Susan M. [6 ]
Dunger, David B. [3 ]
Wareham, Nicholas [2 ]
Sandhu, Manjinder S. [2 ]
Ong, Ken K. [2 ,3 ]
Korbonits, Marta [1 ]
机构
[1] Barts & London Med Sch, John Vane Sci Ctr, Dept Endocrinol, London EC1M 6BQ, England
[2] Univ Cambridge, Addenbrookes Hosp, Inst Metab Sci, Med Res Council Epidemiol Unit, Cambridge CB0 0QQ, England
[3] Univ Cambridge, Addenbrookes Hosp, Dept Paediat, Cambridge CB0 0QQ, England
[4] INSERM, U780, Inst Federatif Rech 69, F-94807 Villejuif, France
[5] Univ Paris 11, Fac Med, F-91405 Orsay, France
[6] Univ Bristol, Dept Social Med, Bristol BS8 1TQ, Avon, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1210/jc.2008-0366
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The GH secretagogue receptor type 1a gene (GHSR) encodes the cognate receptor of ghrelin, a gut hormone that regulates food intake and pituitary GH secretion. Previous studies in U.S. families and a German population suggested GHSR to be a candidate quantitative locus for association with human obesity and growth. Aim: The aim of the study was to test common genetic variation in GHSR for association with body size in children and adults. Methods: Sequencing was performed to systematically identify novel single nucleotide polymorphisms (SNPs) in GHSR. A set of three haplotype-tagging SNPs that captured all the genetic variation in GHSR was identified. These three haplotype-tagging SNPs were then genotyped in three large population-based U.K. cohort studies (two adult and one childhood cohort) comprising 5807 adults and 843 children. Results: No significant genotype or haplotype associations were found with adult or childhood height, weight, or body mass index. Conclusion: Common variation in GHSR is not associated with body size in U. K. adults or children.
引用
收藏
页码:4158 / 4161
页数:4
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