Quantitative trait loci for fasting glucose in young Europeans replicate previous findings for type 2 diabetes in 2q23-24 and other locations

被引:8
作者
Fradin, Delphine
Heath, Simon
Lathrop, Mark
Bougneres, Pierre
机构
[1] Hop St Vincent de Paul, INSERM, U561, Dept Pediat Endocrinol, F-75014 Paris, France
[2] INSERM, U561, Paris, France
[3] Ctr Natl Genotypage, Evry, France
[4] Equipe Accueil Univ Paris V, Paris, France
关键词
D O I
10.2337/db06-1329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Long before reaching diagnostic cutoff levels for type 2 diabetes, fasting glucose can be a powerful risk marker for this disease. We conducted a genome-wide search for fasting glucose as a quantitative trait in 412 young European sib-pairs including obese children, with adjustment for sex, age, and BMI. We identified more quantitative trait loci specific to fasting glucose and more significant than would be found by simple chance estimated by permutation tests. The strongest linkage was on chromosome 2q (logarithm of odds [LOD] = 3.00) in a region previously linked to type 2 diabetes as a disease. We also found linkage signals of fasting glucose with 7q (LOD = 2.03), Sq (1.28), 17p (2.12), 17q (1.4), and Ilp (1.33). These findings suggest that the quantitative genetics of fasting glucose could contribute to the search for type 2 diabetes genes.
引用
收藏
页码:1742 / 1745
页数:4
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