Further evidence for genetic association of CACNA1C and schizophrenia: New risk loci in a Han Chinese population and a meta-analysis

被引:36
作者
Zheng, Fanfan [1 ,2 ]
Zhang, Yanling [1 ,2 ,3 ]
Xie, Wuxiang [4 ]
Li, Wenqiang [5 ,6 ]
Jin, Chao [7 ]
Mi, Weifeng [1 ,2 ]
Wang, Fang [1 ,2 ]
Ma, Wenbin [7 ]
Ma, Cuicui [7 ]
Yang, Yongfeng [5 ,6 ]
Du, Bo [8 ]
Li, Keqing [8 ]
Liu, Chenxing [1 ,2 ]
Wang, Lifang [1 ,2 ]
Lu, Tianlan [1 ,2 ]
Zhang, Hongyan [1 ,2 ]
Wang, Yun [9 ,10 ]
Lu, Lin [11 ]
Lv, Luxian [5 ,6 ]
Zhang, Dai [1 ,2 ,12 ,13 ]
Yue, Weihua [1 ,2 ]
机构
[1] Peking Univ, Inst Mental Hlth, Beijing 100191, Peoples R China
[2] Peking Univ, Minist Hlth, Key Lab Mental Hlth, Beijing 100191, Peoples R China
[3] Beijing Aerosp Gen Hosp, Dept Nephrol, Beijing 100076, Peoples R China
[4] Capital Med Univ, Affiliated Beijing Anzhen Hosp, Beijing Inst Heart Lung & Blood Vessel Dis, Dept Epidemiol, Beijing 100029, Peoples R China
[5] Xinxiang Med Univ, Affiliated Hosp 2, Dept Psychiat, Xinxiang 453002, Henan, Peoples R China
[6] Henan Mental Hosp, Henan Key Lab Biol Psychiat, Xinxiang 453002, Henan, Peoples R China
[7] Jinzhou Kangning Hosp, Jinzhou 121013, Liaoning, Peoples R China
[8] Hebei Mental Hlth Ctr, Baoding 071000, Hebei, Peoples R China
[9] Peking Univ, Hlth Sci Ctr, Neurosci Res Inst, Beijing 100191, Peoples R China
[10] Peking Univ, Hlth Sci Ctr, Minist Educ & Hlth, Dept Neurobiol,Key Lab Neurosci, Beijing 100191, Peoples R China
[11] Peking Univ, Natl Inst Drug Dependence, Beijing 100191, Peoples R China
[12] Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China
[13] Peking Univ, Inst Brain Res, PKU IDG McGoven, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
CACNA1C; rs1006737; Schizophrenia; Genetic association; Case-control study; Meta-analysis; GENOME-WIDE; BIPOLAR DISORDER; POLYMORPHISM; SYMPTOMS; ALLELE; BIAS; TWIN;
D O I
10.1016/j.schres.2013.12.003
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
CACNA1C (12p13.3) has been implicated as a susceptibility gene for schizophrenia by several replicated genome wide association studies. While these results have been consistent among studies in European populations, the findings in East Asian populations have varied. To test whether CACNA1C is a risk gene for schizophrenia, we conducted a case-control study in 5897 schizophrenic patients and 6323 healthy control subjects selected from Han Chinese population. Our study replicated the positive associations of rs1006737 (P = 0.0108, OR = 1.16, 95% CI: 1.03-1.29) and rs1024582 (P = 0.0062, OR = 1.18, 95% CI: 1.05-1.33), and identified a novel risk locus, rs2007044 (P = 0.0053, OR = 1.08, 95% CI: 1.02-1.14). A meta-analysis of rs1006737 combining our study and previous studies was conducted in a total of 8222 schizophrenia cases and 24,661 healthy controls. In the meta-analysis, the association between rs1006737 and schizophrenia remained significant (OR = 1.14, 95% CI: 1.07-1.22, P = 0.0001). Stratified analysis showed no heterogeneity between East Asian and European ancestries (chi(2)[1] = 0.07, P = 0.795), and the difference in pooled ORs between ancestries was not significant (Z = 0.25, P = 0.801). Our results provide further support for associations of rs1006737 and rs1024582 with schizophrenia, identify a new risk locus rs2007044 in a Han Chinese population, and further establish CACNA1C as an important susceptibility gene for the disease across world populations. Crown Copyright (C) 2013 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 110
页数:6
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