No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population

被引:7
作者
Liu, Yansong [2 ]
Cheng, Zaohuo [1 ]
Wang, Jun [1 ]
Jin, Chunhui [1 ]
Yuan, Jianmin [1 ]
Wang, Guoqiang [1 ]
Zhang, Fuquan [1 ]
Zhao, Xudong [2 ]
机构
[1] Wuxi Mental Hlth Ctr, Wuxi 214151, Jiangsu, Peoples R China
[2] Tongji Univ, Shanghai East Hosp, Dept Psychosomat Med, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
Schizophrenia; CSMD1; rs10503253; VARIANT; RISK; MICRORNA;
D O I
10.1186/s12888-016-0923-5
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Schizophrenia (SCZ) is a complex, heritable, and devastating psychiatric disorder. Recent genome-wide association studies have identified a single-nucleotide polymorphism (SNP; rs10503253) in the CUB and SUSHI multiple domains 1 (CSMD1) gene as a risk factor for SCZ. In this study, we investigated whether the rs10503253 in CSMD1 contributes to the risk of SCZ in a Han Chinese population. Methods: We conducted a case-control study in a population from eastern China, involving 1378 SCZ patients and 1091 unrelated healthy controls, using the ligase detection reaction-polymerase chain reaction method to genotype the rs10503253 polymorphism in the CSMD1 gene. Results: No significant association was found between the SCZ patients and controls for any allele or genotype frequency of the SNP rs10503253 (all P > 0.05). Conclusions: Our findings do not support an association between CSMD1 rs10503253 and SCZ in a Han Chinese population.
引用
收藏
页数:5
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