Association of cytokine Th2 gene polymorphisms with autoimmune thyroid diseases in Tunisian population

摘要

Abstract Autoimmune thyroid diseases (AITD) including Graves' disease (GD) and Hashimoto's thyroiditis (HT) are complex genetic diseases. Th2 cytokines act on the development of AITD. This study was conducted on Tunisian patients with AITD to investigate the association of Th2 cytokine gene polymorphisms and haplotype combination with GD or HT risk. A total of 156 controls, 160 patients with HT and 88 patients with GD were genotyped for IL‐4 rs2243250, IL‐5 rs2069812, IL‐6 rs1800796 and IL‐13 rs1800925 polymorphisms by PCR‐RFLP. The AITD risk was assessed by a logistic regression analysis using the SNP stats statistical program. False‐positive report probability (FPRP) was estimated to evaluate significant findings. IL‐13 rs1800925 was associated with GD, after adjustment for age and gender, in codominant, dominant and allele genetic models ( p ?=?.0072; p ?=?.0018; p ?=?.012, respectively). Significant association of the IL‐6 rs1800796C/G genotype with GD was also detected ( p ?=?.025). Furthermore, increased risk of HT was still found for IL‐13 rs1800925T allele ( p ?=?.039, OR?=?1.39) and for IL‐4 rs2243250T/T genotype both in codominant ( p ?=?.033, OR?=?2.59) and recessive ( p ?=?.011, OR?=?2.73) models after adjustment for age and gender. Interestingly, haplotype analysis performed on the IL‐4, IL‐5 and IL‐13 genes revealed a high risk of HT with CTT haplotype ( p ?=?.008, OR?=?2.12). However, the CCT haplotype is a protective factor (OR?=?0.36). Patients carrying the CT haplotype with only one minor allele had a moderate risk of HT (OR?=?1.56). The FPRP analysis showed that the association of IL‐13 rs1800925 polymorphism with GD and HT and the association of CTT haplotype with HT were noteworthy. In conclusion, the IL‐4, IL‐5, IL‐6 and IL‐13 polymorphism may play a role in susceptibility to GD and HT in the Tunisian population. Furthermore, gene–gene interaction between the IL‐4, IL‐5 and IL‐13 significantly increases the risk of AITD. Further studies with larger numbers of individuals are needed to confirm the results.