Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis

To comprehensively evaluate the association between rs7517847 and rs2201841 polymorphisms in the Interleukin-23 (IL-23) receptor gene and ankylosing spondylitis (AS), a meta-analysis was performed. The Pubmed, Embase, MEDLINE, Cochrane, China National Knowledge Infrastructure (CNKI), VIP, Wanfang an...

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Main Authors: Bin Xu, Jian-xiong Ma, Xin-long Ma, Hao-bo Jia, Rui Feng, Li-yan Xu
Format: Article
Language:English
Published: PeerJ Inc. 2015-04-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/910.pdf
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author Bin Xu
Jian-xiong Ma
Xin-long Ma
Hao-bo Jia
Rui Feng
Li-yan Xu
author_facet Bin Xu
Jian-xiong Ma
Xin-long Ma
Hao-bo Jia
Rui Feng
Li-yan Xu
author_sort Bin Xu
collection DOAJ
description To comprehensively evaluate the association between rs7517847 and rs2201841 polymorphisms in the Interleukin-23 (IL-23) receptor gene and ankylosing spondylitis (AS), a meta-analysis was performed. The Pubmed, Embase, MEDLINE, Cochrane, China National Knowledge Infrastructure (CNKI), VIP, Wanfang and China Biology Medicine disc (CBMdisc) databases were searched to identify eligible studies on rs7517847 and rs2201841 polymorphisms in the IL-23 receptor gene and AS that were published through September 2014. Data of interest were extracted from each study, and the meta-analysis was performed using STATA 12.0. Four studies were eligible for the meta-analysis and included a total patient population of 2,465. With regards to rs7517847, the current study showed that the genotype GG and allele G might play a protective role during AS (OR = 0.76, 95% CI [0.59–0.99]; OR = 0.88, 95% CI [0.78–0.99] for homozygote and allelic models, respectively). However, according to the meta-analysis, there was no statistical association between the genotype or allele of rs2201841 and an individual’s susceptibility to AS in all genetic models. In conclusion, it was the IL-23 rs7517847 polymorphism rather than the rs2201841 polymorphism that had a statistical association with AS. Nevertheless, more evidence is needed to confirm this result. Consequently, it is necessary to carry out more high-quality studies to confirm the associations between these two single nucleotide polymorphisms and AS.
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spelling doaj.art-61e71351d5d446bd9281f9a200cc5c542023-12-02T22:00:14ZengPeerJ Inc.PeerJ2167-83592015-04-013e91010.7717/peerj.910910Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysisBin Xu0Jian-xiong Ma1Xin-long Ma2Hao-bo Jia3Rui Feng4Li-yan Xu5Biomechanics Laboratory of Orthopaedic Institute of Tianjin Hospital, Tianjin, ChinaBiomechanics Laboratory of Orthopaedic Institute of Tianjin Hospital, Tianjin, ChinaBiomechanics Laboratory of Orthopaedic Institute of Tianjin Hospital, Tianjin, ChinaBiomechanics Laboratory of Orthopaedic Institute of Tianjin Hospital, Tianjin, ChinaBiomechanics Laboratory of Orthopaedic Institute of Tianjin Hospital, Tianjin, ChinaBiomechanics Laboratory of Orthopaedic Institute of Tianjin Hospital, Tianjin, ChinaTo comprehensively evaluate the association between rs7517847 and rs2201841 polymorphisms in the Interleukin-23 (IL-23) receptor gene and ankylosing spondylitis (AS), a meta-analysis was performed. The Pubmed, Embase, MEDLINE, Cochrane, China National Knowledge Infrastructure (CNKI), VIP, Wanfang and China Biology Medicine disc (CBMdisc) databases were searched to identify eligible studies on rs7517847 and rs2201841 polymorphisms in the IL-23 receptor gene and AS that were published through September 2014. Data of interest were extracted from each study, and the meta-analysis was performed using STATA 12.0. Four studies were eligible for the meta-analysis and included a total patient population of 2,465. With regards to rs7517847, the current study showed that the genotype GG and allele G might play a protective role during AS (OR = 0.76, 95% CI [0.59–0.99]; OR = 0.88, 95% CI [0.78–0.99] for homozygote and allelic models, respectively). However, according to the meta-analysis, there was no statistical association between the genotype or allele of rs2201841 and an individual’s susceptibility to AS in all genetic models. In conclusion, it was the IL-23 rs7517847 polymorphism rather than the rs2201841 polymorphism that had a statistical association with AS. Nevertheless, more evidence is needed to confirm this result. Consequently, it is necessary to carry out more high-quality studies to confirm the associations between these two single nucleotide polymorphisms and AS.https://peerj.com/articles/910.pdfAnkylosing spondylitisSNPsMeta-analysisInterleukin-23 receptor
spellingShingle Bin Xu
Jian-xiong Ma
Xin-long Ma
Hao-bo Jia
Rui Feng
Li-yan Xu
Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis
PeerJ
Ankylosing spondylitis
SNPs
Meta-analysis
Interleukin-23 receptor
title Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis
title_full Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis
title_fullStr Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis
title_full_unstemmed Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis
title_short Association between rs7517847 and rs2201841 polymorphisms in IL-23 receptor gene and risk of ankylosing spondylitis: a meta-analysis
title_sort association between rs7517847 and rs2201841 polymorphisms in il 23 receptor gene and risk of ankylosing spondylitis a meta analysis
topic Ankylosing spondylitis
SNPs
Meta-analysis
Interleukin-23 receptor
url https://peerj.com/articles/910.pdf
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