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dc.contributor.author Bene, László
dc.contributor.author Füst, György
dc.contributor.author Fekete, Béla
dc.contributor.author Kovacs A
dc.contributor.author Horváth, Laura
dc.contributor.author Prohászka, Zoltán
dc.contributor.author Miklos K
dc.contributor.author Palos G
dc.contributor.author Daha M
dc.contributor.author Farkas, Henriette
dc.contributor.author Varga, Lilian
dc.date.accessioned 2018-10-10T08:51:09Z
dc.date.available 2018-10-10T08:51:09Z
dc.date.issued 2003
dc.identifier 0037865427
dc.identifier.citation pagination=1186-1192; journalVolume=48; journalIssueNumber=6; journalTitle=DIGESTIVE DISEASES AND SCIENCES;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/6377
dc.identifier.uri doi:10.1023/A:1023793502456
dc.description.abstract Few data are available on measurements of serum concentrations of complement proteins in inflammatory bowel disease (IBD). Therefore we measured serum levels of C3, C4, and C1-esterase inhibitor (C1-INH) as well as C-reactive protein (CRP) in 167 patients with Crohn's disease (CD) and 111 patients with ulcerative colitis (UC). Median serum concentrations of C3 and C1-INH were significantly higher in CD than in UC. According to multiple logistic regression analysis adjusted to age, sex, activity of disease, and presence of extraintestinal manifestations, IBD patients with high-normal (≥ 128%, ≥75th percentile) C1-INH concentrations had significantly (0.0275) higher odds ratio to have a diagnosis of CD than UC. Patients with high-normal C3 (≥ 1.40 g/liter) and high (≥20 mg/liter) CRP concentrations had an even higher odds ratio of a CD diagnosis (P = 0.0132). Our findings indicate that measurement of C3, C 1-INH, and CRP can be used as an additional marker to pANCA/ASCA for distinguishing patients with CD and UC.
dc.relation.ispartof urn:issn:0163-2116
dc.title High normal serum levels of C3 and C1 inhibitor, two acute-phase proteins belonging to the complement system, occur more frequently in patients with Crohn's disease than ulcerative colitis
dc.type Journal Article
dc.date.updated 2018-09-02T10:00:07Z
dc.language.rfc3066 en
dc.identifier.mtmt 1359487
dc.identifier.wos 000182851300025
dc.identifier.pubmed 12822883
dc.contributor.department SE/AOK/K/III. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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