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Association of TIMP-4 gene polymorphism with the risk of osteoarthritis in the Korean population

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dc.contributor.authorLee, Hee Jae-
dc.contributor.authorLee, Geon-Hee-
dc.contributor.authorNah, Seong-su-
dc.contributor.authorLee, Kyu Hoon-
dc.contributor.authorYang, Hyung-in-
dc.contributor.authorKim, Young-Myeong-
dc.contributor.authorChun, Wanjoo-
dc.contributor.authorHong, Seung-jae-
dc.contributor.authorKim, Sung Soo-
dc.date.accessioned2022-12-21T01:55:22Z-
dc.date.available2022-12-21T01:55:22Z-
dc.date.issued2008-07-
dc.identifier.issn0172-8172-
dc.identifier.issn1437-160X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/178165-
dc.description.abstractDue to an imbalance in the MMP:TIMP ratio determined a tissue damage in arthritis, it is hypothesized that polymorphic variations of the TIMP genes are associated with regulation of the MMP:TIMP balance. To test this hypothesis, the presence of single nucleotide polymorphisms (SNPs) located in the human TIMP-2 and TIMP-4 genes was confirmed in the Korean RA and OA patients. We performed a case-control study comprising 109 unrelated Korean OA patients, 177 unrelated Korean RA patients and 175 healthy subjects. There were statistically significant differences in the genotype distribution and allele frequencies of the C/T polymorphism of TIMP-4 gene between OA and control groups (P = 0.0002 and P = 0.001, respectively). However, no significant association between TIMP-2 polymorphisms and OA was observed. Also, no difference was observed when allele or genotype frequencies of both TIMP-2 and TIMP-4 gene polymorphisms were compared between RA and controls. We demonstrated that the C/T polymorphism which is located on the 3'-untranslational regions of the TIMP-4 gene might be associated with susceptibility to OA patients.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherSpringer Verlag-
dc.titleAssociation of TIMP-4 gene polymorphism with the risk of osteoarthritis in the Korean population-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1007/s00296-008-0545-4-
dc.identifier.scopusid2-s2.0-49949152187-
dc.identifier.wosid000256474800004-
dc.identifier.bibliographicCitationRheumatology International, v.28, no.9, pp 845 - 850-
dc.citation.titleRheumatology International-
dc.citation.volume28-
dc.citation.number9-
dc.citation.startPage845-
dc.citation.endPage850-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRheumatology-
dc.relation.journalWebOfScienceCategoryRheumatology-
dc.subject.keywordPlusSERUM MATRIX METALLOPROTEINASES-
dc.subject.keywordPlusDISEASE-ASSOCIATED VARIANTS-
dc.subject.keywordPlusD-RECEPTOR GENE-
dc.subject.keywordPlusTISSUE INHIBITOR-
dc.subject.keywordPlusSYSTEMATIC ANALYSIS-
dc.subject.keywordPlusSUSCEPTIBILITY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusARTHRITIS-
dc.subject.keywordAuthorTIMP-4-
dc.subject.keywordAuthorTIMP-2-
dc.subject.keywordAuthorpolymorphism-
dc.subject.keywordAuthorosteoarthritis-
dc.subject.keywordAuthorrheumatoid arthritis-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00296-008-0545-4-
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서울 의과대학 (DEPARTMENT OF REHABILITATION MEDICINE)
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