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Association between the three functional miR-146a single-nucleotide polymorphisms, rs2910164, rs57095329, and rs2431697, and autoimmune disease susceptibility: A meta-analysis

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dc.contributor.authorPark, Robin-
dc.contributor.authorLee, Won Jin-
dc.contributor.authorJi, Jong Dae-
dc.date.accessioned2021-09-03T17:40:01Z-
dc.date.available2021-09-03T17:40:01Z-
dc.date.created2021-06-16-
dc.date.issued2016-11-
dc.identifier.issn0891-6934-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/87039-
dc.description.abstractStudies suggest associations between the miR-146a single nucleotide polymorphisms (SNPs) and susceptibility to autoimmune diseases. However, the results are inconsistent and inconclusive. Therefore, the aim of this study was to arrive at a conclusion about the association between the three functional miR-146a SNPs and autoimmune disease risk. Studies were identified through PubMed/MEDLINE searches for studies published up to January 2016 using as keywords rs2910164, rs57095329, rs2431697, and miR-146a polymorphisms. Thirty studies were included in the meta-analysis. The SNP rs2910164 G>C was found to be associated with increased risk of multiple sclerosis (CC + CG versus GG, OR = 1.25, 95% CI: 1.01-1.55), with decreased risks of psoriasis (C versus G, OR = 0.81, 95% CI: 0.69-0.96; CC versus GC + GG, OR = 0.73, 95% CI: 0.56-0.94), Behcet's disease (CC versus GC + GG, OR = 0.60, 95% CI: 0.50-0.73), asthma (C versus G, OR = 0.80, 95% CI: 0.69-0.93; CC versus GC + GG, OR = 0.65, 95% CI: 0.48-0.86), and uveitis (CC + CG versus GG, OR = 0.61, 95% CI: 0.49-0.77). The SNP rs2431697 C>T was found to be associated with an increased risk of SLE (T versus C, OR = 1.26, 95% CI: 1.15-1.38; TC + TT versus CC, OR = 1.28, 95% CI: 1.03-1.58; TT versus TC + CC, OR = 1.40, 95% CI: 1.21-1.62). The SNP rs57095329 A>G was found to be associated with an increased risk of SLE (G versus C, OR = 1.25, 95% CI: 1.17-1.35). The miR-146a SNPs rs2910164, rs57095329, rs2431697 are associated with susceptibility to certain autoimmune diseases. However, for other autoimmune diseases, they may be protective or insignificant.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectSYSTEMIC-LUPUS-ERYTHEMATOSUS-
dc.subjectMULTIPLE-SCLEROSIS SUSCEPTIBILITY-
dc.subjectINFLAMMATORY-BOWEL-DISEASE-
dc.subjectETS-1 GENE POLYMORPHISMS-
dc.subjectGENOME-WIDE ASSOCIATION-
dc.subjectRHEUMATOID-ARTHRITIS-
dc.subjectBEHCETS-DISEASE-
dc.subjectCHINESE POPULATION-
dc.subjectULCERATIVE-COLITIS-
dc.subjectKINASE IRAK1-
dc.titleAssociation between the three functional miR-146a single-nucleotide polymorphisms, rs2910164, rs57095329, and rs2431697, and autoimmune disease susceptibility: A meta-analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorJi, Jong Dae-
dc.identifier.doi10.3109/08916934.2016.1171854-
dc.identifier.scopusid2-s2.0-84964413006-
dc.identifier.wosid000388765700002-
dc.identifier.bibliographicCitationAUTOIMMUNITY, v.49, no.7, pp.451 - 458-
dc.relation.isPartOfAUTOIMMUNITY-
dc.citation.titleAUTOIMMUNITY-
dc.citation.volume49-
dc.citation.number7-
dc.citation.startPage451-
dc.citation.endPage458-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusSYSTEMIC-LUPUS-ERYTHEMATOSUS-
dc.subject.keywordPlusMULTIPLE-SCLEROSIS SUSCEPTIBILITY-
dc.subject.keywordPlusINFLAMMATORY-BOWEL-DISEASE-
dc.subject.keywordPlusETS-1 GENE POLYMORPHISMS-
dc.subject.keywordPlusGENOME-WIDE ASSOCIATION-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusBEHCETS-DISEASE-
dc.subject.keywordPlusCHINESE POPULATION-
dc.subject.keywordPlusULCERATIVE-COLITIS-
dc.subject.keywordPlusKINASE IRAK1-
dc.subject.keywordAuthorAutoimmunity-
dc.subject.keywordAuthorpolymorphism-
dc.subject.keywordAuthormiR-146a-
dc.subject.keywordAuthormeta-analysis-
dc.subject.keywordAuthorsusceptibility-
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