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Association between interleukin-10 polymorphisms and juvenile idiopathic arthritis: a meta-analysis

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dc.contributor.authorJung, Jae Hyun-
dc.contributor.authorKim, Jae-Hoon-
dc.contributor.authorSong, Gwan Gyu-
dc.contributor.authorChoi, Sung Jae-
dc.date.accessioned2022-04-18T11:42:33Z-
dc.date.available2022-04-18T11:42:33Z-
dc.date.created2022-04-18-
dc.date.issued2022-02-
dc.identifier.issn2724-5276-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/140293-
dc.description.abstractINTRODUCTION: The aim of this review is to investigate IL-10 polymorphisms (-1082 G/A, -819 C/T, and -592 C/A) and their association with susceptibility to JIA. EVIDENCE ACQUISITION: A meta-analysis was conducted after database search for relevant articles (MEDLINE and EMBASE). EVIDENCE SYNTHESIS: A total of seven studies involving 1495 patients and 1670 controls were considered in the meta-analysis. There was no association between the IL-10 -1082 G/A, -819 C/T, and -592 C/A polymorphisms and JIA in allele contrast and any of the genetic models (allele contrast: odds ratio [OR] 0.90, 95% confidence interval [CI] 0.791.02, P=0.09; OR=0.97, 95% CI 0.83-1.13, P=0.68; OR=0.92, 95% CI 0.81-1.06, P=0.24, respectively). In subgroup analysis, none of the subtypes of JIA including systemic, rheumatoid factor (RF)-positive polyarticular, RF-negative polyarticular, and oligoarticular was not significantly associated with IL-10 polymorphism. Meta-analysis of the IL-10 haplotype revealed no association between GCC, ACC, and ATA haplotypes and JIA. CONCLUSIONS: This meta-analysis showed that IL-10 polymorphisms were not associated with risk of JIA.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherEDIZIONI MINERVA MEDICA-
dc.subjectGENE POLYMORPHISMS-
dc.subjectSUSCEPTIBILITY-
dc.subjectCYTOKINE-
dc.subjectIL-10-
dc.subjectINFLAMMATION-
dc.subjectDIFFICULT-
dc.titleAssociation between interleukin-10 polymorphisms and juvenile idiopathic arthritis: a meta-analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Jae Hyun-
dc.identifier.doi10.23736/S2724-5276.18.05369-0-
dc.identifier.scopusid2-s2.0-85126422001-
dc.identifier.wosid000768657300011-
dc.identifier.bibliographicCitationMINERVA PEDIATRICS, v.74, no.1, pp.81 - 89-
dc.relation.isPartOfMINERVA PEDIATRICS-
dc.citation.titleMINERVA PEDIATRICS-
dc.citation.volume74-
dc.citation.number1-
dc.citation.startPage81-
dc.citation.endPage89-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPediatrics-
dc.relation.journalWebOfScienceCategoryPediatrics-
dc.subject.keywordPlusGENE POLYMORPHISMS-
dc.subject.keywordPlusSUSCEPTIBILITY-
dc.subject.keywordPlusCYTOKINE-
dc.subject.keywordPlusIL-10-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusDIFFICULT-
dc.subject.keywordAuthorInterleukin-10-
dc.subject.keywordAuthorGenetic polymorphism-
dc.subject.keywordAuthorJuvenile arthritis-
dc.subject.keywordAuthorMeta-analysis-
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