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Associations between the FAS-670 A/G,-1377 G/A, and FASL-844 T/C polymorphisms and susceptibility to systemic lupus erythematosus: a meta-analysis

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dc.contributor.authorLee, Y. H.-
dc.contributor.authorSong, G. G.-
dc.date.accessioned2021-09-03T22:29:43Z-
dc.date.available2021-09-03T22:29:43Z-
dc.date.created2021-06-18-
dc.date.issued2016-07-
dc.identifier.issn0392-856X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88240-
dc.description.abstractObjective The aim of this study was to determine whether the FAS, and FASL polymorphisms are associated with susceptibility to systemic lupus erythematosus (SLE). Methods A meta-analysis was conducted on the associations between the FAS -670 AIG, FAS-1377 GIA, and FASL-844 TIC polymorphisms and SLE. Results A total of eleven articles met the study inclusion criteria. Meta-analysis indicated an association between SLE and the FAS-670 AIG polymorphism in the dominant model (OR=0.629, 95% CI=0.409-0.967, p=0.035). Stratification by ethnicity indicated an association between the FAS-670 GG+GA genotype and SLE in Asian populations (OR=0.464, 95% CI=0.218-0.988, p=0.046). Meta-analysis indicated an association between SLE and the FAS-1377 AA+AG genotype (OR=0.712, 95% CI=0.528 - 0.961, p=0.027), and an association between SLE and the FASL +844 C allele was found (OR=1.377, 95% CI=1.162 - 1.633, p=2.3x10(-4)). Meta-analyses using the recessive model or homozygote contrast showed the same pattern as the meta-analysis of the FASL +844 C allele, that is, a significant association with SLE. Conclusion This meta-analysis demonstrates that the FAS-670 AIG, FAS-1377 GIA, and FASL-844 TIC polymorphisms are associated with susceptibility to SLE.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherCLINICAL & EXPER RHEUMATOLOGY-
dc.subjectFAS GENE POLYMORPHISMS-
dc.subjectRHEUMATOID-ARTHRITIS-
dc.subjectAPO-1/FAS PROMOTER-
dc.subjectAPOPTOSIS-
dc.subjectPOPULATION-
dc.subjectSCLEROSIS-
dc.subjectREGION-
dc.subjectRISK-
dc.subjectSLE-
dc.subjectA/G-
dc.titleAssociations between the FAS-670 A/G,-1377 G/A, and FASL-844 T/C polymorphisms and susceptibility to systemic lupus erythematosus: a meta-analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Y. H.-
dc.contributor.affiliatedAuthorSong, G. G.-
dc.identifier.scopusid2-s2.0-84984804345-
dc.identifier.wosid000383927800010-
dc.identifier.bibliographicCitationCLINICAL AND EXPERIMENTAL RHEUMATOLOGY, v.34, no.4, pp.634 - 640-
dc.relation.isPartOfCLINICAL AND EXPERIMENTAL RHEUMATOLOGY-
dc.citation.titleCLINICAL AND EXPERIMENTAL RHEUMATOLOGY-
dc.citation.volume34-
dc.citation.number4-
dc.citation.startPage634-
dc.citation.endPage640-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRheumatology-
dc.relation.journalWebOfScienceCategoryRheumatology-
dc.subject.keywordPlusFAS GENE POLYMORPHISMS-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusAPO-1/FAS PROMOTER-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordPlusSCLEROSIS-
dc.subject.keywordPlusREGION-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusSLE-
dc.subject.keywordPlusA/G-
dc.subject.keywordAuthorsystemic lupus erythematosus-
dc.subject.keywordAuthorFAS-
dc.subject.keywordAuthorpolymorphism-
dc.subject.keywordAuthormeta-analysis-
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