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基于汉族人群 GWAS 数据和精神疾病基因组学联盟的 GABRB2 多态性与精神分裂症风险的荟萃分析。

Meta-analysis of GABRB2 polymorphisms and the risk of schizophrenia combined with GWAS data of the Han Chinese population and psychiatric genomics consortium.

机构信息

Peking University Sixth Hospital, Beijing, China.

Peking University Institute of Mental Health, Beijing, China.

出版信息

PLoS One. 2018 Jun 12;13(6):e0198690. doi: 10.1371/journal.pone.0198690. eCollection 2018.

Abstract

Schizophrenia (SCZ) is a severe psychiatric disorder with evidence of a strong genetic component in the complex etiologies. Some studies indicated that gamma-aminobutyric acid (GABA)A receptor β2 subunit gene (GABRB2) was associated with SCZ. Other studies reported a negative association. Moreover, the results of two previous meta-analyses of GABRB2 with SCZ were inconsistent and the sample sizes were limited. Therefore, an updated meta-analysis combined with genome-wide association study (GWAS) data of the Han Chinese population and Psychiatric Genomics Consortium (PGC) was performed. Available case-control and family-based genetic data were extracted from association studies, and the GWAS data were included. The findings showed no association between six single-nucleotide polymorphisms of GABRB2 (rs6556547, rs1816071, rs1816072, rs194072, rs252944, and rs187269) and SCZ in a total of 51,491 patients and 74,667 controls. The ethnic subgroup analysis revealed no significant association in Asian populations. Since the PGC data of SCZ (SCZ-PGC, 2014) contained 3 studies of Asian populations (1866 patients and 3418 controls), only the data of European samples in SCZ-PGC were used for the meta-analysis of the Caucasian population in the present study. The result still showed no association in the Caucasian population. In conclusion, the present meta-analysis on combined data from GWASs of the Han Chinese population and PGC suggested that GABRB2 polymorphisms might not be associated with SCZ.

摘要

精神分裂症 (SCZ) 是一种严重的精神疾病,其复杂的病因中有强有力的遗传因素证据。一些研究表明,γ-氨基丁酸 (GABA)A 受体 β2 亚基基因 (GABRB2) 与 SCZ 有关。其他研究则报告了阴性关联。此外,先前两项关于 GABRB2 与 SCZ 的荟萃分析结果不一致,且样本量有限。因此,进行了一项包含汉族人群全基因组关联研究 (GWAS) 数据和精神疾病基因组学联盟 (PGC) 的更新荟萃分析。从关联研究中提取了可用的病例对照和基于家系的遗传数据,并纳入了 GWAS 数据。研究结果显示,GABRB2 的 6 个单核苷酸多态性(rs6556547、rs1816071、rs1816072、rs194072、rs252944 和 rs187269)与 51491 名患者和 74667 名对照者的 SCZ 之间无关联。亚组分析显示亚洲人群中无显著关联。由于 PGC 的 SCZ 数据(SCZ-PGC,2014 年)包含 3 项亚洲人群研究(1866 名患者和 3418 名对照者),因此本研究仅使用 SCZ-PGC 中欧洲样本的数据进行了白种人群的荟萃分析。结果显示白种人群中也无关联。综上所述,本研究对汉族人群 GWAS 与 PGC 联合数据进行的荟萃分析提示 GABRB2 多态性可能与 SCZ 无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1573/5997335/73b9e8f18828/pone.0198690.g001.jpg

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