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

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作者
Bálint Bérczi
Gellért Gerencsér
Nelli Farkas
Péter Hegyi
Gábor Veres
Judit Bajor
László Czopf
Hussain Alizadeh
Zoltán Rakonczay
Éva Vigh
Bálint Erőss
Kata Szemes
Zoltán Gyöngyi
机构
[1] Medical School,Department of Public Health Medicine
[2] University of Pécs,Department of Translational Medicine
[3] Institute of Bioanalysis,1st Department of Pediatrics
[4] Medical School,Department of Gastroenterology
[5] University of Pécs,Department of Haematology
[6] MTA-SZTE Translational Gastroenterology Research Group,Department of Pathophysiology
[7] Institute for Translational Medicine,Department of Radiology
[8] University of Pécs,undefined
[9] First Department of Medicine,undefined
[10] University of Pécs,undefined
[11] Semmelweis University,undefined
[12] First Department of Medicine,undefined
[13] University of Pécs,undefined
[14] Division of Cardiology and Angiology,undefined
[15] First Department of Medicine,undefined
[16] University of Pécs,undefined
[17] First Department of Medicine,undefined
[18] University of Pécs,undefined
[19] University of Szeged,undefined
[20] Medical School,undefined
[21] University of Pécs,undefined
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摘要
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.
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