Anti-Saccharomyces cerevisiae mannan antibodies in inflammatory bowel disease:: comparison of different assays and correlation with clinical features

被引:22
作者
Annese, V
Piepoli, A
Perri, F
Lombardi, G
Latiano, A
Napolitano, G
Corritore, G
Vandewalle, P
Poulain, D
Colombel, JF
Andriulli, A
机构
[1] Osped CSS IRCCS, UOC Gastroenterol, Dipartimento Med Gen & Specialist, Div Gastroenterol, I-71013 San Giovanni Rotondo, Italy
[2] Hop Huriez CH & U Lille, Lab Parasitol Mycol, Lille, France
[3] Hop Huriez CH & U Lille, Serv Hepatogastroenterol, Lille, France
关键词
D O I
10.1111/j.1365-2036.2004.02258.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Anti-Saccharomyces cerevisiae mannan antibodies have been proposed as a new serological marker associated with Crohn's disease. However, their clinical value is still unclear; furthermore, a standardization of anti-S. cerevisiae mannan measurements is lacking. Aim: In this study, we aimed to assess the correlation between anti-S. cerevisiae mannan detection and specific clinical features in Crohn's disease and ulcerative colitis. Moreover. we tested the concordance of four different anti-S. cerevisiae mannan assays. Materials and methods: Serum samples from 196 patients with Crohn's disease. 197 patients with ulcerative colitis and 100 unrelated healthy controls were tested for anti-S. cerevisiae mannan with a standard enzyme-linked immunosorbent assay method (Lille) by one of the authors (VP). Subsequently, 60 randomly selected serum samples (2 7 Crohn's disease, 2 8 ulcerative colitis and five healthy controls) were tested for anti-S. cerevisiae mannan with three different commercial kits. Results: With the Lille assay, anti-S. cerevisiae mannan were detected in 100 of 196 patients with Crohn's disease (51%; P < 0.0001 vs. controls), 32 of 197 patients with ulcerative colitis (16%; P < 0.02 vs. controls), and six of 100 controls (6%,). No correlation between presence of anti-S. cerevisiae mannan and specific clinical features was found in both ulcerative colitis and Crohn's disease patients. The percentages of anti-S. cerevisiae mannan detected with four different assays ranged from 28 (Bouty) up to 43% (Inova), but these differences did not reach statistical significance. The concordance rate of anti-S. cerevisiae mannan detection in the four assays was very low (11 concordant results of 60 samples, 18.30%) (k = 0.15). No improvement of the concordance rate was obtained by modifying the suggested cut-off values (k = 0.20). Conclusion: In this study, we confirm that anti-S. cerevisiae mannan are significantly more frequent in Crohn's disease patients compared with ulcerative colitis patients (P < 0.0001) and controls. However, no correlation with clinical features was found in both ulcerative colitis and Crohn's disease. The low prevalence of anti-S. cerevisiae mannan, at least in our population, and the low concordance rate between different assays, makes the clinical role of this marker questionable.
引用
收藏
页码:1143 / 1152
页数:10
相关论文
共 26 条
[21]   Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in affected and unaffected relatives of patients with Crohn's disease [J].
Sutton, CL ;
Yang, H ;
Li, Z ;
Rotter, JI ;
Targan, SR ;
Braun, J .
GUT, 2000, 46 (01) :58-63
[22]   Marker antibody expression stratifies Crohn's disease into immunologically homogeneous subgroups with distinct clinical characteristics [J].
Vasiliauskas, EA ;
Kam, LY ;
Karp, LC ;
Gaiennie, J ;
Yang, H ;
Targan, SR .
GUT, 2000, 47 (04) :487-496
[23]   Comparative study of ASCA (Anti-Saccharomyces cerevisiae antibody) assays in inflammatory bowel disease [J].
Vermeire, S ;
Joossens, S ;
Peeters, M ;
Monsuur, F ;
Marien, G ;
Bossuyt, X ;
Groenen, P ;
Vlietinck, R ;
Rutgeerts, P .
GASTROENTEROLOGY, 2001, 120 (04) :827-833
[24]   NATURAL-HISTORY OF INDETERMINATE COLITIS [J].
WELLS, AD ;
MCMILLAN, I ;
PRICE, AB ;
RITCHIE, JK ;
NICHOLLS, RJ .
BRITISH JOURNAL OF SURGERY, 1991, 78 (02) :179-181
[25]   Characterization of oligosaccharides from an antigenic mannan of Saccharomyces cerevisiae [J].
Young, M ;
Davies, MJ ;
Bailey, D ;
Gradwell, MJ ;
Smestad-Paulsen, B ;
Wold, JK ;
Barnes, RMR ;
Hounsell, EF .
GLYCOCONJUGATE JOURNAL, 1998, 15 (08) :815-822
[26]  
ZWEIG MH, 1993, CLIN CHEM, V39, P561