Coeliac disease (CD) is a multigenic and multifactorial enteropathy triggered by gluten-composing
proteins. A possible involvement of the intestinal Aminopeptidase N (APN) was investigated by an
association analysis. SSCP analysis detected four variants at position 281, 378, 956 and 2957
(referred to no. g178535, GenBank) that were studied in 193 Italian CD families. The haplotypic
combinations were determined from family segregation and pairwise linkage disequilibria
(D′ = D/Dmax) between the polymorphic sites were calculated. Significant D′ values ranged between 0.78
and 0.31. Association with CD was tested by TDT (Transmission Disequilibrium Test) utilizing as
markers the nucleotide substitutions and their haplotypic combinations. No statistically significant
transmission distortion to the probands or to their clinically silent sibs was observed. Our data
exclude an involvement in CD of the tested markers and of further undetected variation in strong
linkage disequilibrium (D′ ≅ 1) with them. The power of the test was not adequate to detect an
association with an unknown polymorphism which is not in complete linkage disequilibrium with
those analysed.