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Association between interleukin-18 polymorphisms and systemic lupus erythematosus: a meta-analysis

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dc.contributor.authorSong, Gwan Gyu-
dc.contributor.authorChoi, Sung Jae-
dc.contributor.authorJi, Jong Dae-
dc.contributor.authorLee, Young Ho-
dc.date.accessioned2021-09-06T03:47:32Z-
dc.date.available2021-09-06T03:47:32Z-
dc.date.created2021-06-14-
dc.date.issued2013-03-
dc.identifier.issn0301-4851-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/103799-
dc.description.abstractThe aim of this study was to determine whether the three functional interleukin-18 (IL-18) promoter -607 C/A (rs1946518), -137 G/C (rs187238), and -1297 C/T (rs360719) polymorphisms confer susceptibility to systemic lupus erythematosus (SLE) in ethnically different populations. Meta-analysis was conducted on the associations between these IL-18 polymorphisms and SLE using; (1) allele contrast, (2) the recessive model, (3) the dominant model, and (4) the additive model. A total of 11 comparisons (nine studies) involving 8,453 subjects (2,928 SLE patients and 5,525 controls) were included in the meta-analysis. In all study subjects, meta-analysis showed no association between SLE and the IL-18 -607 C allele (odds ratio [OR] = 1.065, 95 % confidence interval [CI] = 0.870-1.303, p = 0.541). However, stratification by ethnicity indicated a significant association between this allele and SLE in Europeans (OR = 0.864, 95 % CI = 0.757-0.986, p = 0.031), but not in Asians (OR = 1.230, 95 % CI = 0.902-1.676, p = 0.190). Meta-analyses showed the same pattern for the IL-18 -607 C allele using the dominant and additive models. Meta-analysis of the IL-18 -137 G/C polymorphism showed no association between SLE and the IL-18 -137 G allele in all study subjects (OR = 0.916, 95 % CI = 0.836-1.003, p = 0.057), but stratification by ethnicity indicated a significant association between this allele and SLE in Asians (OR = 0.792, 95 % CI = 0.629-0.997, p = 0.047), but not in Europeans (OR = 0.930, 95 % CI = 0.839-1.032, p = 0.171). Furthermore, meta-analysis showed that the IL-18 -1297 C allele was significantly associated with SLE in all study subjects and in Europeans (OR = 1.240, 95 % CI = 1.052-1.482, p = 0.010 and OR = 1.303, 95 % CI = 1.050-1.617, p = 0.016). This meta-analysis shows that the IL-18 -607 C/A and -1297 C/T polymorphism are associated with the development of SLE in Europeans, and the IL-18 -137 G/C polymorphism is associated with SLE in Asians.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectPROMOTER POLYMORPHISMS-
dc.subjectGENE POLYMORPHISMS-
dc.subjectCHINESE PATIENTS-
dc.subjectIL-18-
dc.subjectDISEASE-
dc.subjectSUSCEPTIBILITY-
dc.subjectARTHRITIS-
dc.subjectSLE-
dc.subjectNEPHRITIS-
dc.subjectTRIALS-
dc.titleAssociation between interleukin-18 polymorphisms and systemic lupus erythematosus: a meta-analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Gwan Gyu-
dc.contributor.affiliatedAuthorChoi, Sung Jae-
dc.contributor.affiliatedAuthorJi, Jong Dae-
dc.contributor.affiliatedAuthorLee, Young Ho-
dc.identifier.doi10.1007/s11033-012-2344-y-
dc.identifier.scopusid2-s2.0-84878385877-
dc.identifier.wosid000314535600057-
dc.identifier.bibliographicCitationMOLECULAR BIOLOGY REPORTS, v.40, no.3, pp.2581 - 2587-
dc.relation.isPartOfMOLECULAR BIOLOGY REPORTS-
dc.citation.titleMOLECULAR BIOLOGY REPORTS-
dc.citation.volume40-
dc.citation.number3-
dc.citation.startPage2581-
dc.citation.endPage2587-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusPROMOTER POLYMORPHISMS-
dc.subject.keywordPlusGENE POLYMORPHISMS-
dc.subject.keywordPlusCHINESE PATIENTS-
dc.subject.keywordPlusIL-18-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusSUSCEPTIBILITY-
dc.subject.keywordPlusARTHRITIS-
dc.subject.keywordPlusSLE-
dc.subject.keywordPlusNEPHRITIS-
dc.subject.keywordPlusTRIALS-
dc.subject.keywordAuthorInterleukin-18-
dc.subject.keywordAuthorPolymorphism-
dc.subject.keywordAuthorSystemic lupus erythematosus-
dc.subject.keywordAuthorMeta-analysis-
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