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AIRE 基因多态性与类风湿关节炎的关联:病例对照研究的系统评价和荟萃分析。

Association between AIRE gene polymorphism and rheumatoid arthritis: a systematic review and meta-analysis of case-control studies.

机构信息

Department of Public Health Medicine, Medical School, University of Pécs, Pécs, Hungary.

Institute of Bioanalysis, Medical School, University of Pécs, Pécs, Hungary.

出版信息

Sci Rep. 2017 Oct 26;7(1):14096. doi: 10.1038/s41598-017-14375-z.

Abstract

Autoimmune regulator (AIRE) is a transcription factor that functions as a novel player in immunological investigations. In the thymus, it has a pivotal role in the negative selection of naive T-cells during central tolerance. Experimental studies have shown that single nucleotide polymorphism (SNP) alters transcription of the AIRE gene. SNPs thereby provide a less efficient negative selection, propagate higher survival of autoimmune T-cells, and elevate susceptibility to autoimmune diseases. To date, only rheumatoid arthritis (RA) has been analysed by epidemiological investigations in relation to SNPs in AIRE. In our meta-analysis, we sought to encompass case-control studies and confirm that the association between SNP occurrence and RA. After robust searches of Embase, PubMed, Cochrane Library, and Web of Science databases, we found 19 articles that included five independent studies. Out of 11 polymorphisms, two (rs2075876, rs760426) were common in the five case-control studies. Thus, we performed a meta-analysis for rs2075876 (7145 cases and 8579 controls) and rs760426 (6696 cases and 8164 controls). Our results prove that rs2075876 and rs760426 are significantly associated with an increased risk of RA in allelic, dominant, recessive, codominant heterozygous, and codominant homozygous genetic models. These findings are primarily based on data from Asian populations.

摘要

自身免疫调节因子(AIRE)是一种转录因子,作为免疫研究的新成员发挥作用。在胸腺中,它在中枢耐受过程中对幼稚 T 细胞的阴性选择中起着关键作用。实验研究表明,单核苷酸多态性(SNP)改变了 AIRE 基因的转录。SNP 从而提供了较低效的阴性选择,促进了自身免疫性 T 细胞的更高存活率,并增加了自身免疫性疾病的易感性。迄今为止,仅对类风湿关节炎(RA)进行了与 AIRE 中的 SNP 相关的流行病学研究分析。在我们的荟萃分析中,我们试图包括病例对照研究,并证实 SNP 发生与 RA 之间的关联。经过对 Embase、PubMed、Cochrane 图书馆和 Web of Science 数据库的稳健搜索,我们找到了包含五个独立研究的 19 篇文章。在 11 个多态性中,有两个(rs2075876、rs760426)在五个病例对照研究中是常见的。因此,我们对 rs2075876(7145 例和 8579 例对照)和 rs760426(6696 例和 8164 例对照)进行了荟萃分析。我们的结果证明 rs2075876 和 rs760426 与 RA 的风险增加在等位基因、显性、隐性、杂合子共显性和纯合子共显性遗传模型中显著相关。这些发现主要基于亚洲人群的数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c88a/5658331/dd49eff67d5a/41598_2017_14375_Fig1_HTML.jpg

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