Objectives. To study, by sequential screening for gliadin antibodies (
GA) and endomysial antibodies (EMA), the prevalence and clinical chara
cteristics of coeliac disease (CD) in adult IDDM patients. Subjects an
d measurements. A series comprising 1664 diabetes patients [848 with I
DDM, 745 with non-insulin-dependent diabetes (NIDDM) and 71 with secon
dary diabetes] were screened for GA. IgA- or IgG-GA positive sera were
analysed for EMA. Results, IgA-GA were more frequent in all the diabe
tes subgroups (13.7% in IDDM,12.3% in NIDDM and 23.9% in secondary dia
betes, P < 0.001 in all three cases) than among healthy blood donors (
4.7%). Two patients with NIDDM had CD. Of the IDDM group (n = 848), 8
had previously diagnosed CD and 14 more (of whom 7 could be biopsied)
were EMA positive. All had villous atrophy, The minimum prevalence of
CD (including probable cases) in IDDM was 2.6% (22/848). Patients with
previously known CD had more symptoms (P < 0.001), more deficiency st
ates (P < 0.001) and more autoimmune diseases (P < 0.04) than those id
entified by screening, IDDM patients with a diabetes duration of 31-40
years were characterised by a higher prevalence of CD than patients w
ith a duration of less than 30 years (6.7% vs. 1.7%; P < 0.02). Conclu
sions. Serial analysis of GA and EMA confirmed a high prevalence of CD
in adult IDDM (2.6%). False-positive IgA-GA test results are frequent
in patients with diabetes, irrespective of type. EMA analysis is the
preferable screening tool for CD in diabetes.