Diagnostic value of anti-Saccharomyces cerevisiae and antineutrophil cytoplasmic autoantibodies in inflammatory bowel disease

被引:34
作者
Peeters, M
Joossens, S
Vermeire, S
Vlietinck, R
Bossuyt, X
Rutgeerts, P
机构
[1] Univ Hosp Gasthuisberg, Dept Human Genet, Gastroenterol Unit, B-3000 Louvain, Belgium
[2] Univ Hosp Gasthuisberg, Immunol Lab, B-3000 Louvain, Belgium
关键词
D O I
10.1016/S0002-9270(00)02406-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Correct diagnosis of inflammatory bowel disease (IBD), especially the differentiation between Crohn's disease (CD) and ulcerative colitis (UC), is highly important toward treatment and prognosis. Serological markers are noninvasive diagnostic tools that could be of value in differentiating CD from UC, in cases of indeterminate colitis, and in the identification of subgroups in IBD. The aim of this study was to evaluate the diagnostic accuracy of perinuclear antineutrophil cytoplasmic (pANCA) and anti-Saccharomyces cerevisiae antibodies (ASCA) for IBD. METHODS: ASCA and pANCA were studied in a large cohort of consecutive IBD patients (n = 582: 407 CD, 147 UC, and 28 indeterminate colitis), patients with non-IBD diarrheal illnesses (n = 74), and healthy controls (n = 157). An indirect immunofluorescence technique and a standardized ELISA were performed for detection of pANCA and ASCA, respectively. RESULTS: prevalence of ASCA and pANCA was high in CD patients (59.7%) and UC (49.7%;) patients, respectively. Positivity for both markers was significantly lower in healthy and non-IBD controls. Accuracy data (sensitivity, specificity, PPV, and NPV, respectively) for differentiating IBD from controls are as follows: ASCA(+): 60% (243/407), 91% (345/378), 88% (243/276), and 68% (345/509); pANCA(+): 50% (73/147), 95% (605/638), 69% (73/106), and 89% (605/679); ASCA(+)/pANCA(-): 56% (229/407), 94% (355/378), 91% (229/252), and 67% (355/533); and pANCA(+)/ASCA(-): 44% (65/147), 97% (620/638), 78% (65/83), and 88% (620/702). CONCLUSIONS: Specificity of serological markers for LED is high, but low sensitivity makes them less useful as diagnostic tests. The combination of tests is probably more powerful, although, clinical subgroups still need to be defined. The usefulness of these markers in indeterminate colitis needs to be studied prospectively. (C) 2001 by Am. Cell. of Gastroenterology.
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页码:730 / 734
页数:5
相关论文
共 22 条
[1]
ANTINEUTROPHIL ANTIBODIES IN INFLAMMATORY BOWEL-DISEASE - PREVALENCE AND DIAGNOSTIC ROLE [J].
CAMBRIDGE, G ;
RAMPTON, DS ;
STEVENS, TRJ ;
MCCARTHY, DA ;
KAMM, M ;
LEAKER, B .
GUT, 1992, 33 (05) :668-674
[2]
ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES IN ULCERATIVE-COLITIS - COMPARISON WITH OTHER COLITIDES DIARRHEAL ILLNESSES [J].
DUERR, RH ;
TARGAN, SR ;
LANDERS, CJ ;
SUTHERLAND, LR ;
SHANAHAN, F .
GASTROENTEROLOGY, 1991, 100 (06) :1590-1596
[3]
INCIDENCE OF INFLAMMATORY BOWEL-DISEASE IN NORTHERN FRANCE (1988-1990) [J].
GOWERROUSSEAU, C ;
SALOMEZ, JL ;
DUPAS, JL ;
MARTI, R ;
NUTTENS, MC ;
VOTTE, A ;
LEMAHIEU, M ;
LEMAIRE, B ;
COLOMBEL, JF ;
CORTOT, A .
GUT, 1994, 35 (10) :1433-1438
[5]
Serologic testing for inflammatory bowel disease [J].
Hoffenberg, EJ ;
Fidanza, S ;
Sauaia, A .
JOURNAL OF PEDIATRICS, 1999, 134 (04) :447-452
[6]
CLASSIFICATION OF INFLAMMATORY BOWEL-DISEASE [J].
LENNARDJONES, JE .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1989, 24 :2-6
[7]
ANTIBODY TO SACCHAROMYCES CEREVISIAE (BAKERS-YEAST) IN CROHNS-DISEASE [J].
MAIN, J ;
MCKENZIE, H ;
YEAMAN, GR ;
KERR, MA ;
ROBSON, D ;
PENNINGTON, CR ;
PARRATT, D .
BRITISH MEDICAL JOURNAL, 1988, 297 (6656) :1105-1106
[8]
Inflammatory bowel disease: Re-evaluation of the diagnosis in a prospective population based study in south eastern Norway [J].
Moum, B ;
Ekbom, A ;
Vatn, MH ;
Aadland, E ;
Sauar, J ;
Lygren, I ;
Schulz, T ;
Stray, N ;
Fausa, O .
GUT, 1997, 40 (03) :328-332
[9]
*NAT COMM CLIN LAB, 1991, C24A NCCLS, V11
[10]
OVERLAP IN SPECTRUM OF NONSPECIFIC INFLAMMATORY BOWEL-DISEASE - COLITIS INDETERMINATE [J].
PRICE, AB .
JOURNAL OF CLINICAL PATHOLOGY, 1978, 31 (06) :567-577