Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/40232
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dc.contributor.authorChen, D.Y.en_US
dc.contributor.author林季千zh_TW
dc.contributor.authorChen, Y.M.en_US
dc.contributor.authorChen, H.H.en_US
dc.contributor.authorHsieh, C.W.en_US
dc.contributor.authorLin, C.C.en_US
dc.contributor.authorLan, J.L.en_US
dc.date2009zh_TW
dc.date.accessioned2014-06-06T08:03:28Z-
dc.date.available2014-06-06T08:03:28Z-
dc.identifier.issn0315-162Xzh_TW
dc.identifier.urihttp://hdl.handle.net/11455/40232-
dc.description.abstractObjective. Interleukin 18 (IL-18) has a central role in the pathogenesis of adult-onset Still's disease (AOSD). We investigated the functional association of -607 (C/A) IL-I8 promoter polymorphisms with disease course in Chinese patients with AOSD. Methods. Sequence-specific primer polymerase chain reaction and the restriction fragment-length polymorphism method were used to analyze the genotypes of IL-18 promoter polymorphism at position -607 in 96 unrelated patients with AOSD and 164 ethnically-matched healthy controls. Serum IL-18 levels were determined using ELISA in patients with active untreated AOSD. Results. Significantly lower frequencies of single-nucleotide polymorphism -607/AA were observed in patients with AOSD compared to healthy controls (18.8% vs 31.1%, respectively; p < 0.05). Median levels of serum IL-18 were significantly lower in AOSD patients with AA genotype compared to those with CA genotype or CC genotype (147.5 pg/ml vs 410.5 pg/ml or 262.4 pg/ml, respectively; both p < 0.05). Significantly lower IL-18 levels were demonstrated in AOSD patients with a monocyclic systemic course than in those with a polycyclic systemic course or a chronic articular course. The AA genotype was more frequently observed in patients with monocyclic systemic course, which had the best prognosis, than in those with the other 2 disease courses. In contrast, a lower frequency of the AA genotype than the CA or the CC genotype was observed in patients with chronic disabling arthritis (5.5% vs 25.0% or 19.2%, respectively). Conclusion. The SNP -607/AA genotype with lower IL-18 levels might be a genetically protective factor for the occurrence of AOSD in the Chinese population, against progression of chronic disabling arthritis. (First Release August 15 2009: J Rheumatol 2009;36:2284-9; doi:10.3899/jrheum.090316)en_US
dc.language.isoen_USzh_TW
dc.relationJournal of Rheumatologyen_US
dc.relation.ispartofseriesJournal of Rheumatology, Volume 36, Issue 10, Page(s) 2284-2289.en_US
dc.relation.urihttp://dx.doi.org/10.3899/jrheum.090316en_US
dc.subjectinterleukin 18en_US
dc.subjectpromoter polymorphismsen_US
dc.subjectdisease courseen_US
dc.subjectchineseen_US
dc.subjectadult-onset still's diseaseen_US
dc.subjectsingle-nucleotide polymorphismsen_US
dc.subjectclinical-manifestationsen_US
dc.subjectpathologicalen_US
dc.subjecttissuesen_US
dc.subjectjapanese populationen_US
dc.subjectcytokine profilesen_US
dc.subjectarthritisen_US
dc.subjectcomplicationsen_US
dc.subjectgenotypeen_US
dc.subjectblooden_US
dc.subjectgammaen_US
dc.titleFunctional Association of Interleukin 18 Gene-607 (C/A) Promoter Polymorphisms with Disease Course in Chinese Patients with Adult-onset Still's Diseaseen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.3899/jrheum.090316zh_TW
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