Association of celiac disease with microsatellite polymorphisms close to the tumor necrosis factor genes

Celiac disease is tightly linked to the MHC class II region on chromosome 6. We have studied two highly polymorphic microsatellite loci, TNFa and b, near the TNF genes in the class III region of the MHC, for evidence of their association to CD, as compared to a control population. Our findings show that the microsatellite allele most significantly associated with the disease is TNFb3, which is found in 86.3% of CD patients versus 24.5% of controls, with allele frequencies of 0.5392 and 0.1290, respectively ( p < 0.001). The TNFa2 allele had a frequency of 0.6122 in CD patients and 0.2627 in controls (< 0.001), with phenotype frequencies of 87.8% and 50.0%, respectively. TNFa6 and -all and TNFb5 have significantly reduced frequencies in CD patients. TNFb3 shows a maximal level of linkage disequilibrium with HLA-DQB1 ∗0201 in celiac patients. However, while the DQB1 ∗0201/TNFa2 haplotype was strongly associated with CD, DQB1 ∗0201 was not significantly in linkage disequilibrium with TNFa2, suggesting that TNFa2 is independently associated with CD. This association could have functional significance as TNFa2 has been correlated with high TNF production.