Objectives: Systemic sclerosis (SSc) is an uncommon autoimmune disease that varies with ethnicity. Single nucleotide polymorphisms (SNPs) in the GTFSI, NFKB1, and TYK2 genes have been reported to be associated with SSc in other populations and in individuals with various autoimmune diseases. This study aimed to investigate the association between these SNPs and susceptibility to SSc in a Chinese Han population.
Method: A case-control study was performed in 343 patients with SSc and 694 ethnically matched healthy controls. SNPs in GTF2I, NFKB1, and TYK2 were genotyped using a Sequenom MassArray iPLEX system. Association analyses were performed using PLINK v1.90 software.
Result: Our study demonstrated that the rs117026326 T allele and the rs73366469 C allele were strongly associated with patients with SSc ( = 6.97E-10 and = 1.33E-08, respectively). Patients carrying the rs117026326 TT genotype and the rs73366469 CC genotype had a strongly increased risk of SSc ( = 6.25E-09 and = 1.67E-08, respectively), and those carrying the rs1599961 AA genotype had a suggestively significantly increased risk of SSc ( = 0.014). Moreover, rs117026326 and rs73366469 were associated with SSc in different genetic models (additive model, dominant model, and recessive model) ( < 0.05) whereas rs1599961 was associated with SSc in the dominant genetic model but not in the addictive and recessive models ( = 0.0026). rs2304256 was not significantly associated with SSc in this study.
Conclusion: rs117026326 and rs73366469 SNPs were strongly associated with SSc in this Chinese Han population. rs1599961 showed a suggestive association with SSc, and no significant association was found between rs2304256 and SSc in this Chinese Han population.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261294 | PMC |
| http://dx.doi.org/10.3389/fimmu.2021.640083 | DOI Listing |
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