V. Annese et al., Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in Crohn's disease and ulcerative colitis: A GISC study, AM J GASTRO, 96(8), 2001, pp. 2407-2412
OBJECTIVES: Recent studies in familial Crohn's disease (CD) have suggested
that anti-Saccharomyces cerevisiae mannan antibodies (ASCAs) may represent
a new specific marker of genetic susceptibility. In this study we aimed to
assess the importance of ASCAs by comparing their presence in a large numbe
r of patients with sporadic and familial occurrence of CD or ulcerative col
itis (UC) and their unaffected relatives.
METHODS: Serum samples from 96 patients with sporadic CD, 97 patients with
sporadic UC. and 50 unrelated healthy controls were tested for ASCAs by a s
tandard ELISA method. Moreover, 73 families with two or more members affect
ed by CD and/or UC were recruited. From these families 58 CD patients, 84 U
C patients, and 216 unaffected first degree relatives were investigated.
RESULTS: ASCAs were detected in 34 of 96 patients with sporadic CD (35%, p
< 0.01 vs controls), I I of 97 patients with sporadic UC (12%), and two of
50 controls (4%). ASCAs were significantly (p < 0.04) more frequent in pati
ents with familial CD (55%) and familial UC (25%) than in sporadic cases. M
oreover, ASCAs were found in 25% of unaffected relatives, and this rate did
not significantly differ in CD, UC, and mixed families (28%, 26%, and 22%,
respectively).
CONCLUSIONS: In this study we confirm that ASCAs occur particularly frequen
tly in CD patients, especially with the presence of a positive family histo
ry. However, they are also significantly increased in UC patients with a fa
mily history and in a considerable number of unaffected relatives of inflam
matory bowel disease families. irrespective of the characteristics of their
families (UC, CD, mixed, ASCA positive, and ASCA negative). The presence o
f ASCAs in unaffected relatives might point toward a genetic predisposition
to either CD or UC. (C) 2001 by Am. Coll. of Gastroenterology.