Replication of genome-wide association studies of type 2 diabetes susceptibility in Japan

被引:135
作者
Horikawa, Yukio
Miyake, Kazuaki
Yasuda, Kazuki
Enya, Mayumi
Hirota, Yushi
Yamagata, Kazuya
Hinokio, Yoshinori
Oka, Yoshitomo
Iwasaki, Naoko
Iwamoto, Yasuhiko
Yamada, Yuichiro
Seino, Yutaka
Maegawa, Hiroshi
Kashiwagi, Atsunori
Yamamoto, Ken
Tokunaga, Katsushi
Takeda, Jun
Kasuga, Masato
机构
[1] Kobe Univ, Grad Sch Med, Chuo Ku, Dept Internal Med,Div Diabet Metab & Endocrinol, Kobe, Hyogo 6500017, Japan
[2] Gifu Univ, Sch Med, Div Mol & Struct, Dept Endocrinol & Diabet, Gifu 5011194, Japan
[3] Gunma Univ, Inst Mol & Cellular Regulat, Biosignal Genome Resource Ctr, Lab Med Genom, Maebashi, Gunma 3718512, Japan
[4] Int Med Ctr Japan, Res Inst, Dept Metab Disorder, Tokyo 1628655, Japan
[5] Osaka Univ, Grad Sch Med, Dept Metab Med, Suita, Osaka 5650871, Japan
[6] Tohoku Univ, Grad Sch Med, Div Mol Metab & Diabet, Sendai, Miyagi 9808574, Japan
[7] Tokyo Womens Med Univ, Ctr Diabet, Dept Med, Tokyo 1628666, Japan
[8] Kyoto Univ, Sch Med, Dept Diabet & Clin Nutr, Kyoto 6068501, Japan
[9] Shiga Univ Med Sci, Dept Med, Div Endocrinol & Metab, Shiga 5202192, Japan
[10] Kyushu Univ, Med Inst Bioregulat, Dept Mol Genet, Fukuoka 8128582, Japan
[11] Univ Tokyo, Grad Sch Med, Dept Human Genet, Tokyo 1130033, Japan
关键词
D O I
10.1210/jc.2008-0452
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In Europeans and populations of European origin, several groups have recently identified novel type 2 diabetes susceptibility genes, including FTO, SLC30A8, HHEX, CDKAL1, CDKN2B, and IGF2BP2, none of which were in the list of functional candidates. Objective and Design: The aim of this study was to replicate in a Japanese population previously identified associations of single nucleotide polymorphisms (SNPs) within 10 candidate loci with type 2 diabetes using a relatively large sample size: 1921 subjects with type 2 diabetes and 1622 normal controls. Results: A total of 15 SNPs were genotyped. Eight SNPs in five loci were found to be associated with type 2 diabetes: rs3802177 [odds ratio (OR) = 1.16 (95% confidence interval (CI) 1.05-1.27); P = 4.5 X 10(-3)] in SLC30A8; rs1111875 [OR = 1.27 (95% CI 1.14-1.40); P = 1.4 X 10(-5)] and rs7923837 [OR = 1.27 (95% CI 1.13 - 1.43); P = 1.0 X 10(-4)] in HHEX; rs10811661 [OR = 1.27 (95% CI 1.15 - 1.40); P = 1.9 X 10(-6)] in CDKN2B; rs4402960 [OR = 1.23 ( 95% CI 1.11 - 1.36); P = 8.1 X 10(-5)] and rs1470579 [OR = 1.18 (95% CI 1.07 - 1.31); P = 8.3 X 10(-4)] in IGF2BP2; and rs7754840 [OR = 1.28 (95% CI 1.17 - 1.41); P = 4.5 X 10(-7)] and rs7756992 [OR = 1.27 ( 95% CI 1.15 - 1.40); P = 9.8 X 10(-7)] inCDKAL1. The first and second strongest associations were found at variants in CDKAL1 and CDKN2B, both of which are involved in the regenerative capacity of pancreatic beta-cells. Conclusion: Some of these variants represent common type 2 diabetes- susceptibility genes in both Japanese and Europeans.
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页码:3136 / 3141
页数:6
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