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Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.

Authors :
Cho YS
Chen CH
Hu C
Long J
Ong RT
Sim X
Takeuchi F
Wu Y
Go MJ
Yamauchi T
Chang YC
Kwak SH
Ma RC
Yamamoto K
Adair LS
Aung T
Cai Q
Chang LC
Chen YT
Gao Y
Hu FB
Kim HL
Kim S
Kim YJ
Lee JJ
Lee NR
Li Y
Liu JJ
Lu W
Nakamura J
Nakashima E
Ng DP
Tay WT
Tsai FJ
Wong TY
Yokota M
Zheng W
Zhang R
Wang C
So WY
Ohnaka K
Ikegami H
Hara K
Cho YM
Cho NH
Chang TJ
Bao Y
Hedman ÅK
Morris AP
McCarthy MI
Takayanagi R
Park KS
Jia W
Chuang LM
Chan JC
Maeda S
Kadowaki T
Lee JY
Wu JY
Teo YY
Tai ES
Shu XO
Mohlke KL
Kato N
Han BG
Seielstad M
Source :
Nature genetics [Nat Genet] 2011 Dec 11; Vol. 44 (1), pp. 67-72. Date of Electronic Publication: 2011 Dec 11.
Publication Year :
2011

Abstract

We conducted a three-stage genetic study to identify susceptibility loci for type 2 diabetes (T2D) in east Asian populations. We followed our stage 1 meta-analysis of eight T2D genome-wide association studies (6,952 cases with T2D and 11,865 controls) with a stage 2 in silico replication analysis (5,843 cases and 4,574 controls) and a stage 3 de novo replication analysis (12,284 cases and 13,172 controls). The combined analysis identified eight new T2D loci reaching genome-wide significance, which mapped in or near GLIS3, PEPD, FITM2-R3HDML-HNF4A, KCNK16, MAEA, GCC1-PAX4, PSMD6 and ZFAND3. GLIS3, which is involved in pancreatic beta cell development and insulin gene expression, is known for its association with fasting glucose levels. The evidence of an association with T2D for PEPD and HNF4A has been shown in previous studies. KCNK16 may regulate glucose-dependent insulin secretion in the pancreas. These findings, derived from an east Asian population, provide new perspectives on the etiology of T2D.

Details

Language :
English
ISSN :
1546-1718
Volume :
44
Issue :
1
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
22158537
Full Text :
https://doi.org/10.1038/ng.1019