Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2

被引:131
作者
Reynisdottir, I
Thorleifsson, G
Benediktsson, R
Sigurdsson, G
Emilsson, V
Einarsdottir, AS
Hjorleifsdottir, EE
Orlygsdottir, GT
Bjornsdottir, GT
Saemundsdottir, J
Halldorsson, S
Hrafnkelsdottir, S
Sigurjonsdottir, SB
Steinsdottir, S
Martin, M
Kochan, JP
Rhees, BK
Grant, SFA
Frigge, ML
Kong, A
Gudnason, V
Stefansson, K
Gulcher, JR
机构
[1] deCODE Genet, Reykjavik, Iceland
[2] Iceland Heart Assoc, Reykjavik, Iceland
[3] Landspitali Univ Hosp, Reykjavik, Iceland
[4] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
关键词
D O I
10.1086/377139
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report a genomewide linkage study of type 2 diabetes ( T2D [MIM 125853]) in the Icelandic population. A list of type 2 diabetics was cross-matched with a computerized genealogical database clustering 763 type 2 diabetics into 227 families. The diabetic patients and their relatives were genotyped with 906 microsatellite markers. A nonparametric multipoint linkage analysis yielded linkage to 5q34-q35.2 (LOD = 2.90, P = 1.29 x 10(-4)) in all diabetics. Since obesity, here defined as body mass index (BMI) greater than or equal to 30 kg/m(2), is a key risk factor for the development of T2D, we studied the data either independently of BMI or by stratifying the patient group as obese ( BMI greater than or equal to 30) or nonobese (BMI < 30). A nonparametric multipoint linkage analysis yielded linkage to 5q34 - q35.2 (LOD = 3.64, P = 2.12 x 10(-5)) in the nonobese diabetics. No linkage was observed in this region for the obese diabetics. Linkage analysis conditioning on maternal transmission to the nonobese diabetics resulted in a LOD score of 3.48 (P = 3.12 x 10(-5)) in the same region, whereas conditioning on paternal transmission led to a substantial drop in the LOD score. Finally, we observed potential interactions between the 5q locus and two T2D susceptibility loci, previously mapped in other populations.
引用
收藏
页码:323 / 335
页数:13
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