Transcription factor-7-like 2 gene variants are strongly associated with type 2 diabetes in Lebanese subjects

被引:22
作者
Nemr, Rita [2 ]
Turki, Amira [3 ]
Echtay, Akram [4 ]
Al-Zaben, Ghadeer S.
Daher, Hoda S.
Irani-Hakime, Noha A. [5 ]
Keleshian, Sose H. [5 ]
Almawi, Wassim Y. [1 ]
机构
[1] Arabian Gulf Univ, Coll Med & Med Sci, Dept Med Biochem, Manama, Bahrain
[2] Univ Med Ctr Rizk Hosp, Dept Endocrinol, Beirut, Lebanon
[3] Univ Monastir, Fac Pharm Monastir, Monastir, Tunisia
[4] Rafic Hariri Univ Hosp, Dept Endocrinol, Beirut, Lebanon
[5] St Georges Univ Hosp, Dept Lab Med, Beirut, Lebanon
关键词
Diabetes; Genome wide association; Replication; TCF7L2; TCF7L2; GENE; JAPANESE POPULATION; ARAB POPULATION; COMMON VARIANTS; REPLICATION; RISK; POLYMORPHISMS; MELLITUS; GLUCOSE;
D O I
10.1016/j.diabres.2012.09.044
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We tested the association of TCF7L2 variants with type 2 diabetes (T2DM) in 691 Lebanese people and 919 controls. rs7901695, rs4506565, rs7903146, rs12243326, rs7895340, and rs12255372 minor allele frequencies were higher in T2DM. Haplotype analysis (rs7901695-rs4506565-rs7903146-rs12243326-rs7895340-rs11196205-rs12255372) identified positively- (2122112, 2222222) and negatively- (1111111) T2DM-associated haplotypes. TCF7L2 is a common T2DM candidate gene in Lebanese people. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:E23 / E27
页数:5
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