The relationship between five widely-evaluated variants in CDKN2A/B and CDKAL1 genes and the risk of type 2 diabetes: A meta-analysis

被引:26
|
作者
Peng, Feng [1 ]
Hu, Dan [2 ]
Gu, Chaohao [3 ]
Li, Xiaobo [4 ,5 ,6 ]
Li, Yuqiong [4 ,5 ,6 ]
Jia, Nan [5 ,6 ]
Chu, Shaoli [5 ,6 ]
Lin, Jinxiu [1 ]
Niu, Wenquan [4 ,6 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Dept Cardiol, Fuzhou, Peoples R China
[2] Fujian Med Univ, Teaching Hosp, Fujian Prov Tumor Hosp, Dept Pathol, Fuzhou, Peoples R China
[3] Sichuan Univ, Coll Comp Sci, Chengdu 610064, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, State Key Lab Med Genom, Shanghai 200030, Peoples R China
[5] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Hypertens, Shanghai 200030, Peoples R China
[6] Shanghai Res Inst Hypertens, Shanghai, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Type; 2; diabetes; CDKN2A/B; CDKAL1; Gene; Variant; Meta-analysis; COMMON VARIANTS; ASSOCIATION ANALYSIS; IGF2BP2; CHINESE; HHEX; POLYMORPHISMS; SLC30A8; SUSCEPTIBILITY; TCF7L2; LOCI;
D O I
10.1016/j.gene.2013.08.075
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The genes encoding two cyclin-dependent kinases-inhibitor-2A/B (CDKN2A/B) and 5 regulatory subunit-associated protein-like 1 (CDKAL1) have been investigated extensively in associations with type 2 diabetes; the results, however, are often irreproducible. We therefore sought to evaluate these associations by performing a meta-analysis on five widely-evaluated variants from the two genes. There were 38 studies (patients/controls: 51,940/52,234) for rs10811661, 16 studies (20,029/24,419) for rs564398 in CDKN2A/B gene, and 27 studies (28,383/47,635) for rs7756992, 26 studies (28,816/31,713) for rs7754840, 21 studies (29,260/38,400) for rs10946398 in CDKAL1 gene. Overall risk estimates for type 2 diabetes conferred by rs10811661-T, rs564398-A, rs7754840-C, rs7756992-G, and rs10946398-C alleles were 1.17 (95% CI: 1.10-1.23; P < 0.0005; I-2 = 83.9%), 1.1 (95% CI: 1.0-121; P = 0.051; I-2 = 883%), 1.24 (95% CI: 1.18-1.3; P < 0.0005; I-2 = 743%), 1.2 (95% CI: 1.11-1.3; P < 0.0005; I-2 = 92.0%), and 1.19 (95% CI: 1.1-129; P < 0.0005; I-2 = 90.8%), respectively. There was evident publication bias for rs564398 and rs7754840. Subgroup analyses by ethnicity showed remarkable divergences in risk estimate for rs564398 between Asians (odds ratio [OR] = 1.01; 95% CI: 0.86-1.19; P = 0.868) and Caucasians (OR = 1.19; 95% CI: 1.03-1.35; P = 0.012) (P < 0.05). For all variants examined, the results of studies in retrospective design or with population-based controls were comparative with that of overall studies. In meta-regression analyses, age was found to exert a significant influence on the association between rs10811661 and type 2 diabetes (P = 0.003), as well as between rs7754840 and gender (P = 0.034). Taken together, our findings provide evidence for a significant contribution of CDKN2A/B gene rs10811661 and CDKAL1 gene rs7756992 and rs10946398 to type 2 diabetes. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:435 / 443
页数:9
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