Associations of gene polymorphisms in interferon‐alpha signature‐related genes with autoimmune thyroid diseases

Interferon (IFN)-alpha treatment predisposes patients to the occurrence of autoimmune thyroid disease (AITD). METHODS: We investigated associations of single nucleotide polymorphisms (SNPs) of molecules participating in the IFN-alpha signature, including rs2304204 and rs2304206 of IFN regulatory factor 3 (IRF3), rs1061501 of IRF7, and rs7708392 of TNFA1P3-interacting protein 1 with serum IFN-alpha levels and AITD in an ethnic Chinese (ie Taiwanese) population. Totally, 319 patients with Graves' disease (GD), 83 patients with Hashimoto's thyroiditis (HT) and 351 healthy controls were recruited. RESULTS: There were increased percentages of the C allele, and CC and TC + CC genotypes of rs1061501 in GD patients compared to the controls. HT patients had higher serum IFN-alpha levels compared to the controls, while there was no difference in serum IFN-alpha levels between patients with GD and controls. However, patients with GD in a remission status had lower serum IFN-alpha levels than those without remission. On the other hand, the C allele of rs1061501 was only associated with serum IFN-alpha levels in patients with HT. CONCLUSIONS: The SNP rs1061501 of IRF7 was associated with the development of GD. Serum IFN-alpha levels were associated with HT, while they might modify the disease status of GD. Moreover, a genetic effect of rs1061501 on regulating serum IFN-alpha production was observed in HT.