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Genetic Studies of Ankylosing Spondylitis in Koreans Confirm Associations with ERAP1 and 2p15 Reported in White Patients

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dc.contributor.authorBang, So-Young-
dc.contributor.authorKim, Tae-Hwan-
dc.contributor.authorLee, Bitnara-
dc.contributor.authorKwon, Eunji-
dc.contributor.authorChoi, Sang Hyun-
dc.contributor.authorLee, Ki Soo-
dc.contributor.authorShim, Seung Cheol-
dc.contributor.authorPope, Angela-
dc.contributor.authorRahman, Proton-
dc.contributor.authorReveille, John D.-
dc.contributor.authorInman, Robert D.-
dc.date.accessioned2022-07-16T22:09:49Z-
dc.date.available2022-07-16T22:09:49Z-
dc.date.created2021-05-11-
dc.date.issued2011-02-
dc.identifier.issn0315-162X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/169156-
dc.description.abstractObjective. Investigators from the Australo-Anglo-American Spondyloarthritis Consortium have reported additional genes associated with ankylosing spondylitis (AS) susceptibility including IL1R2, ANTXR2, and gene deserts at 2p15 and 21q22. We evaluated these new candidate genes in a large cohort of Korean patients with AS. Methods. A group of 1164 patients with AS and 752 healthy controls were enrolled for our study. Eight single-nucleotide polymorphisms (SNP) were analyzed to define genetic association with AS by MassARRAY system. Results. Significant positive associations of AS with endoplasmic reticulum aminopeptidase 1 SNP, rs27037 (p = 1.31 x 10(-4)), and rs27434 (p = 4.59 x 10(-6)), were observed. The rs10865331 of gene desert at 2p15 also showed a significant association with AS (p = 4.63 x 10(-5)). Conclusion. This is the first confirmation in a nonwhite population that genetic polymorphisms of rs27037, rs27434, and rs10865331 are associated with AS, implicating common pathogenetic mechanisms in Korean and white patients with AS. (First Release Nov 1 2010; J Rheumatol 2011; 38:322-4; doi:10.3899/jrheum.100652)-
dc.language영어-
dc.language.isoen-
dc.publisherJ RHEUMATOL PUBL CO-
dc.titleGenetic Studies of Ankylosing Spondylitis in Koreans Confirm Associations with ERAP1 and 2p15 Reported in White Patients-
dc.typeArticle-
dc.contributor.affiliatedAuthorBang, So-Young-
dc.contributor.affiliatedAuthorKim, Tae-Hwan-
dc.identifier.doi10.3899/jrheum.100652-
dc.identifier.scopusid2-s2.0-79551717945-
dc.identifier.wosid000287173000022-
dc.identifier.bibliographicCitationJOURNAL OF RHEUMATOLOGY, v.38, no.2, pp.322 - 324-
dc.relation.isPartOfJOURNAL OF RHEUMATOLOGY-
dc.citation.titleJOURNAL OF RHEUMATOLOGY-
dc.citation.volume38-
dc.citation.number2-
dc.citation.startPage322-
dc.citation.endPage324-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRheumatology-
dc.relation.journalWebOfScienceCategoryRheumatology-
dc.subject.keywordPlusGENOME-WIDE ASSOCIATION-
dc.subject.keywordPlusPOLYMORPHISMS-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusVARIANTS-
dc.subject.keywordAuthorANKYLOSING SPONDYLITIS-
dc.subject.keywordAuthorERAP1-
dc.subject.keywordAuthor2p15-
dc.subject.keywordAuthorKOREA-
dc.subject.keywordAuthorSINGLE-NUCLEOTIDE POLYMORPHISM-
dc.identifier.urlhttps://www.jrheum.org/content/38/2/322-
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