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dc.contributor.authorSahebari, M
dc.contributor.authorRezaieyazdi, Z
dc.contributor.authorNakhjavani, MJ
dc.contributor.authorHatef, M
dc.contributor.authorMahmoudi, M
dc.contributor.authorAkhlaghi, S
dc.date.accessioned2018-08-26T08:05:31Z
dc.date.available2018-08-26T08:05:31Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49838
dc.description.abstractRecent researches suggest that imbalance in apoptotic process may lead to susceptibility to systemic lupus erythematosus (SLE). Production of pro-inflammatory cytokines, such as IL-18, has important role in autoimmune process in lupus. There are cumulative data on the pro-apoptotic role of IL-18, in the Fas-mediated apoptosis. Soluble Fas (Apo/1-CD95) is a marker of apoptosis that appears to increase in serum of SLE patients. Previous studies demonstrated increasing serum concentrations of soluble Fas (sFas) and IL-18 in SLE. To assess the correlation between serum concentrations of sFas and IL-18 in SLE patients, 114 SLE patients were selected randomly at the different stages of disease activity according to SLEDAI2K. IL-18 and sFas serum concentrations were compared in patients and fifty randomly selected healthy volunteers. The correlations of IL-18 and sFas serum concentrations with SLEDAI2K and with each other were evaluated in patients. There were a significant difference between serum concentrations of sFas and IL-18 in the case and control groups (P = 0.001). There was a significant correlation between serum concentrations of sFAS and IL-18 in SLE patients (P < 0.0001, r = 0.411). The elevations of IL-18 and sFas(Apo/1-CD95) serum concentrations in SLE patients are significantly correlated.
dc.language.isoEnglish
dc.relation.ispartofRHEUMATOLOGY INTERNATIONAL
dc.subjectSoluble Fas (CD95/Apo-1)
dc.subjectInterleukine-18(IL-18)
dc.subjectSystemic lupus erythematosus
dc.subjectApoptosis
dc.titleCorrelation between serum concentrations of soluble Fas (CD95/Apo-1) and IL-18 in patients with systemic lupus erythematosus
dc.typeArticle
dc.citation.volume32
dc.citation.issue3
dc.citation.spage601
dc.citation.epage606
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1007/s00296-010-1633-9


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