Analysis of Polymorphisms of the Interleukin-18 Gene in Type 1 Diabetes and Hardy-Weinberg Equilibrium Testing
Szeszko JS., Howson JMM., Cooper JD., Walker NM., Twells RCJ., Stevens HE., Nutland SL., Todd JA.
Recently, the interleukin-18 cytokine gene (IL18) was reported to be associated with type 1 diabetes. In the present report, we calculated that the reported genotypes of the two 5′ region/promoter single nucleotide polymorphisms (SNPs), −607 (C→A) (rs1946518) and −137 (G→C) (rs187238), were not in Hardy-Weinberg equilibrium (HWE). We therefore investigated the association of the −607 and −137 SNPs in a U.K. type 1 diabetic Caucasian case-control collection (1,560 case and 1,715 control subjects tested at −607 and 4,323 case and 4,610 control subjects tested at −137) as well as a type 1 diabetic Caucasian collection comprised of families of European ancestry (1,347 families tested at −137 and 1,356 families tested at −607). No evidence for association with type 1 diabetes was found, including for the −607 A/A and C/A genotypes. To evaluate whether common variation elsewhere in the gene was associated with disease susceptibility, we analyzed eight IL18 tag SNPs in a type 1 diabetic case-control collection (1,561 case and 1,721 control subjects). No evidence for association was obtained (P = 0.11). We conclude that common allelic variation in IL18 is unlikely to contribute substantially to type 1 diabetes susceptibility in the populations tested and recommend routine application of tests for HWE in population-based studies for genetic association.