Meta-Analyses of KIF6 Trp719Arg in Coronary Heart Disease and Statin Therapeutic Effect

被引:24
|
作者
Peng, Ping [1 ,2 ]
Lian, Jiangfang [1 ]
Huang, R. Stephanie [3 ]
Xu, Limin [2 ]
Huang, Yi [2 ]
Ba, Yanna [1 ,2 ]
Yang, Xi [1 ]
Huang, Xiaoyan [1 ]
Dong, Changzhen [2 ]
Zhang, Lina [2 ]
Ye, Meng [2 ]
Zhou, Jianqing [1 ]
Duan, Shiwei [2 ]
机构
[1] Ningbo Univ, Lihuili Hosp, Ningbo Med Ctr, Ningbo 315211, Zhejiang, Peoples R China
[2] Ningbo Univ, Affiliated Hosp, Sch Med, Ningbo 315211, Zhejiang, Peoples R China
[3] Univ Chicago, Dept Med, Chicago, IL 60637 USA
来源
PLOS ONE | 2012年 / 7卷 / 12期
基金
中国国家自然科学基金;
关键词
KINESIN-LIKE PROTEIN-6; ARTERY-DISEASE; MYOCARDIAL-INFARCTION; POLYMORPHISM; ASSOCIATION; RISK; GENE; POPULATION; VARIANTS; BIAS;
D O I
10.1371/journal.pone.0050126
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aims: The goal of our study is to assess the contribution of KIF6 Trp719Arg to both the risk of CHD and the efficacy of statin therapy in CHD patients. Methods and Results: Meta-analysis of 8 prospective studies among 77,400 Caucasians provides evidence that 719Arg increases the risk of CHD (P<0.001, HR = 1.27, 95% CI = 1.15-1.41). However, another meta-analysis of 7 case-control studies among 65,200 individuals fails to find a significant relationship between Trp719Arg and the risk of CHD (P = 0.642, OR = 1.02, 95% CI = 0.95-1.08). This suggests that the contribution of Trp719Arg to CHD varies in different ethnic groups. Additional meta-analysis also shows that statin therapy only benefit the vascular patients carry 719Arg allele (P, 0.001, relative ratio (RR) = 0.60, 95% CI = 0.54-0.67). To examine the role of this genetic variant in CHD risk in Han Chinese, we have conducted a case-control study with 289 CHD cases, 193 non-CHD controls, and 329 unrelated healthy volunteers as healthy controls. On post hoc analysis, significant allele frequency difference of 719Arg is observed between female CHD cases and female total controls under the dominant model (P = 0.04, chi(2) = 4.228, df = 1, odd ratio (OR) = 1.979, 95% confidence interval (CI) = 1.023-3.828). Similar trends are observed for post hoc analysis between female CHD cases and female healthy controls (dominant model: P = 0.04, chi(2) = 4.231, df = 1, OR = 2.015, 95% CI = 1.024-3.964). Non-genetic CHD risk factors are not controlled in these analyses. Conclusions: Our meta-analysis demonstrates the role of Trp719Arg of KIF6 gene in the risk of CHD in Caucasians. The meta-analysis also suggests the role of this variant in statin therapeutic response in vascular diseases. Our case-control study suggests that Trp719Arg of KIF6 gene is associated with CHD in female Han Chinese through a post hoc analysis.
引用
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页数:7
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