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几丁质酶 3 样蛋白 1 基因与精神分裂症:一项多中心病例对照研究和荟萃分析的证据。

The chitinase 3-like 1 gene and schizophrenia: evidence from a multi-center case-control study and meta-analysis.

机构信息

Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

出版信息

Schizophr Res. 2010 Feb;116(2-3):126-32. doi: 10.1016/j.schres.2009.12.002. Epub 2010 Jan 3.

Abstract

The chitinase 3-like 1 (CHI3L1) gene acts as a cellular survival factor in response to several environmental and psychosocial stresses. The expression level of CHI3L1 was increased in the hippocampus and prefrontal cortex regions of patients with schizophrenia. Genetic variants of the CHI3L1 gene have been significantly associated with schizophrenia in two distinct ethnic groups, the Chinese and Irish populations. The aims of this study are to confirm the association between the CHI3L1 gene and schizophrenia in a Japanese population using the largest sample size to date (1463 cases and 1795 controls) and perform a meta-analysis of the combined samples (3005 cases, 3825 controls and 601 trios). We found significant associations between single nucleotide polymorphism (SNP) 4/rs4950928 (p=0.009), which is located in the promoter region of the CHI3L1 gene, and haplotypes including this SNP and schizophrenia (the most significant global p<0.001). As the meta-analysis of the combined samples showed significant heterogeneity among studies of SNP3/rs10399805 (p=0.026) and SNP4 (p<0.001), we performed meta-analyses separately in the Japanese (2033 cases and 2365 controls) and Chinese populations (412 cases, 464 controls and 601 trios), the major groups analyzed in association studies of the CHI3L1 gene. The meta-analysis in Japanese populations showed stronger evidence for the association of schizophrenia with SNP4 (p=0.003), while the meta-analysis in Chinese populations showed an association with a different variant (SNP3) (p=0.003). We conclude that the genetic variants in the CHI3L1 gene have ethnic heterogeneity and confer a susceptibility to schizophrenia in Asian populations.

摘要

几丁质酶 3 样蛋白 1(CHI3L1)基因作为一种细胞存活因子,在应对多种环境和心理社会压力中发挥作用。精神分裂症患者的海马体和前额叶皮质区域中 CHI3L1 的表达水平增加。CHI3L1 基因的遗传变异与中国和爱尔兰两个不同种族的精神分裂症显著相关。本研究的目的是使用迄今为止最大的样本量(1463 例病例和 1795 例对照)在日本人群中确认 CHI3L1 基因与精神分裂症之间的关联,并对合并样本(3005 例病例、3825 例对照和 601 个三核苷酸重复)进行荟萃分析。我们发现单核苷酸多态性(SNP)4/rs4950928 (位于 CHI3L1 基因启动子区域)与包括该 SNP 的单倍型之间存在显著关联,与精神分裂症有关(最显著的全局 p<0.001)。由于 SNP3/rs10399805(p=0.026)和 SNP4(p<0.001)的研究之间存在显著的异质性,我们分别在日本(2033 例病例和 2365 例对照)和中国人群(412 例病例、464 例对照和 601 个三核苷酸重复)中进行了荟萃分析,这是 CHI3L1 基因关联研究中的主要人群。日本人群的荟萃分析显示 SNP4 与精神分裂症的关联具有更强的证据(p=0.003),而中国人群的荟萃分析显示与另一个变体(SNP3)有关(p=0.003)。我们的结论是,CHI3L1 基因中的遗传变异具有种族异质性,并赋予亚洲人群易患精神分裂症的倾向。

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