The susceptibility to develop coeliac disease (CD) has a strong genetic component, which is not entirely explained by HLA associations. Two previous genome wide linkage studies have been performed to identify additional loci outside this region. These studies both used a sib-pair design and produced conflicting results.Our aim is to identify non-MHC genetic loci contributing to coeliac disease using a family based linkage study. We performed a genome wide search in 16 highly informative multiply affected pedigrees using 400 microsatellite markers with an average spacing of 10 cM. Linkage analysis was performed using lod score and model free methods.We identified two new potential susceptibility loci with lod scores of 1n9, at 10q23n1, and 16q23n3. Significant, but lower lod scores were found for 6q14 (1n2), 11p11 (1n5), and 19q13n4 (0n9), areas implicated in a previous genome wide study. Lod scores of 0n9 were obtained for both D7S507, which lies 1 cM from the γT-cell receptor gene, and for D2S364, which lies 12 cM from the CTLA4 gene.
Coeliac disease (CD) is a gluten sensitive enteropathy in which dietary exposure to wheat, barley, rye, and possibly oats results in small bowel mucosal atrophy and consequent malabsorption. There is a strong genetic component to disease development as demonstrated by a disease concordance among monozygotic twins of 70-100 % (Polanco et al. 1981 ;Salazar de Souza et al. 1987), and a 30-50 % concordance in Correspondence : Prof. PJ Ciclitira,