TY - JOUR
T1 - Significant linkage of BMI to chromosome 10p in the U.K. population and evaluation of GAD2 as a positional candidate
AU - Groves, Christopher J.
AU - Zeggini, Eleftheria
AU - Walker, Mark
AU - Hitman, Graham A.
AU - Levy, Jonathan C.
AU - O'Rahilly, Stephen
AU - Hattersley, Andrew T.
AU - McCarthy, Mark I.
AU - Wiltshire, Steven
PY - 2006
Y1 - 2006
N2 - 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.
AB - 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.
KW - LD, linkage disequilibrium
KW - LOD, logarithm of odds
KW - QTDT, quantitative transmission-disequilibrium test
KW - QTL, quantitative trait locus
KW - SNP, single nucleotide polymorphism
UR - http://www.scopus.com/inward/record.url?scp=33748316505&partnerID=8YFLogxK
U2 - 10.2337/db05-1674
DO - 10.2337/db05-1674
M3 - Article
C2 - 16731858
AN - SCOPUS:33748316505
SN - 0012-1797
VL - 55
SP - 1884
EP - 1889
JO - Diabetes
JF - Diabetes
IS - 6
ER -