Serologic markers, HLA-DQ2 haplotype, and clinical features suggestive of c
eliac disease were studied to assess their diagnostic value in a multicentr
ic study to detect celiac disease in 675 first-degree relatives of 227 celi
ac probands. Serum IgA-class anti-endomysium and IgA-class anti-gliadin ant
ibodies were positive in 5.8% and 1.9% of relatives, respectively. HLA-DQ2
haplotype was present in 64% of relatives, and the overall rate of celiac d
isease diagnosed by intestinal biopsy was 5.5%. The frequency of HLA-DQ2 in
the celiac patients and controls was 93% and 18%, respectively. The most f
requent clinical features- diarrhea, anemia, food intolerance, and growth r
etardation-were not present in one third of the celiac disease relatives. W
e conclude that the assessment of IgA-class anti-endomysium antibodies alon
e seems a reasonable approach for screening celiac disease in relatives and
cannot be replaced by an accurate clinical anamnesis. HLA-DQ2 haplotype ma
y identify the population with a high genetic susceptibility to celiac dise
ase.