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精神分裂症中 MHC 介导的风险贡献可能反映了更具种族特异性的遗传和合并症背景。

Contribution from MHC-Mediated Risk in Schizophrenia Can Reflect a More Ethnic-Specific Genetic and Comorbid Background.

机构信息

Human Molecular Genetics Laboratory, Rajiv Gandhi Centre for Biotechnology, Trivandrum 695014, India.

Mental Health Centre, Trivandrum 695005, India.

出版信息

Cells. 2022 Aug 30;11(17):2695. doi: 10.3390/cells11172695.

Abstract

The immune system seems to play a significant role in the development of schizophrenia. This becomes more evident with the emerging role of MHC complex and cytokines in schizophrenia. In the recent past, several GWAS have implied that the 6p21 region was associated with schizophrenia. However, the majority of these studies were performed in European populations. Considering tremendous variations in this region and the probability of South Indian populations being quite different from the European gene-pool from an immunogenetic point, the present study was initiated to screen SNPs in the 2.28 MB region, spanning the extended MHC locus, in 492 cases and controls from a South Indian population. We found a very strong association of rs3815087 with schizophrenia at both allelic and genotypic levels with a 7.3-fold increased risk in the recessive model. Interestingly, the association of none of the earlier reported GWAS hits, such as rs3130375, rs3131296, rs9272219, or rs3130297 were found to be replicable in our study population. rs3815087 lies in the 5'UTR region of the psoriasis susceptibility 1 candidate 1 () gene, which further suggests that inflammatory processes might be an important common pathogenic pathway leading to both schizophrenia and psoriasis. The study hints at ethnic specific gene-environment interaction in determining the critical threshold for disease initiation and progression.

摘要

免疫系统似乎在精神分裂症的发展中起着重要作用。这一点随着 MHC 复合物和细胞因子在精神分裂症中的作用的出现而变得更加明显。在最近的过去,几项 GWAS 表明 6p21 区域与精神分裂症有关。然而,这些研究中的大多数都是在欧洲人群中进行的。考虑到该区域的巨大差异,以及从免疫遗传学角度来看,印度南部人群与欧洲基因库的可能性非常不同,因此本研究启动了一项筛选 SNP 的研究,该研究在印度南部人群的 492 例病例和对照中筛选了跨越扩展 MHC 基因座的 2.28MB 区域中的 SNP。我们发现 rs3815087 在等位基因和基因型水平上与精神分裂症有很强的关联,在隐性模型中风险增加了 7.3 倍。有趣的是,我们的研究人群中没有发现之前报道的任何 GWAS 命中,如 rs3130375、rs3131296、rs9272219 或 rs3130297,具有可复制性。rs3815087 位于银屑病易感候选基因 1()基因的 5'UTR 区域,这进一步表明炎症过程可能是导致精神分裂症和银屑病的重要共同致病途径。该研究暗示了在确定疾病起始和进展的关键阈值方面,种族特异性的基因-环境相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e9/9454640/3dfebda7b1cc/cells-11-02695-g001.jpg

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