Significant linkage of BMI to chromosome 10p in the UK population,and evaluation of GAD2 as a positional candidate

被引:21
|
作者
Groves, Christopher J.
Zeggini, Eleftheria
Walker, Mark
Hitman, Graham A.
Levy, Jonathan C.
O'Rahilly, Stephen
Hattersley, Andrew T.
McCarthy, Mark I.
Wiltshire, Steven
机构
[1] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
[3] Univ Newcastle Upon Tyne, Sch Clin Med Sci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Barts & London Queen Marys Sch Med & Dent, Dept Diabet & Metab Med, London, England
[5] Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
[6] Addenbrookes Hosp, Dept Clin Biochem, Cambridge CB2 2QQ, England
[7] Peninsula Med Sch, Ctr Genet Mol, Exeter, Devon, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.2337/db05-1674
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is a major health problem, and many family-based studies have suggested that it has a strong genetic basis. We performed a genome-wide quantitative trait linkage scan for loci influencing BMI in 573 pedigrees from the U.K. We identified genome-wide significant linkage (logarithm of odds = 3.74, between D10S208 and D10S196, genome-wide P = 0.0186) on chromosome 10p. The size of our study population and the statistical significance of our findings provide substantial contributions to the body of evidence for a locus on chromosome 10p. We examined eight single nucleotide polymorphisms (SNPs) in GAD2, which maps to this linkage region, tagging the majority of variation in the gene, and observed marginally significant (0.01 < P < 0.05) associations between four common variants and BMI. However, these SNPs did not account for our evidence of linkage to BMI, and they did not replicate (in direction of effect) the previous associations. We therefore conclude that these SNPs are not the etiological variants underlying this locus. We cannot rule out the possibility that other untagged variations in GAD2 may, in part, be involved, but it is most likely that alternative gene(s) within the broad gene-rich region of linkage on 10p are responsible for variation in body mass and susceptibility to obesity.
引用
收藏
页码:1884 / 1889
页数:6
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