Department of Biomedicine and Prevention, Genetics Section, University of Rome Tor Vergata, 00133 Rome, Italy.
Rheumatology, Department of Medicine, University of Perugia, Piazzale Giorgio Menghini, 1, 06129 Perugia, Italy.
J Immunol Res. 2021 Dec 23;2021:5812136. doi: 10.1155/2021/5812136. eCollection 2021.
Vitamin D is an important hormone involved in various physiologic processes, and its activity is linked to binding with vitamin D receptor (VDR). Genetic polymorphisms in the VDR gene could modulate the expression or function of the receptor and, consequently, alter the effects of vitamin D. Variants in VDR gene have been associated with susceptibility to many illnesses sensitive to vitamin D administration and to autoimmune disorders, but no data are available regarding autoimmune connective tissue diseases in Italian population. We analyzed three VDR polymorphisms in 695 Italian patients with autoimmune connective tissue diseases (308 with systemic lupus erythematosus (SLE), 195 with primary Sjogren's syndrome (pSS), and 192 with rheumatoid arthritis (RA)) and in 246 healthy controls with the aim to evaluate a possible association of VDR SNPs with susceptibility to these diseases in the Italian population. Genotyping of rs2228570, rs7975232, and rs731236 in VDR gene was performed by an allelic discrimination assay. A case/control association study and a genotype/phenotype correlation analysis have been performed. We observed a higher risk to develop SLE for rs2228570 TT genotype ( = 0.029, OR = 1.79). No association was observed between susceptibility to pSS or RA and this SNP, although this variant is significantly less present in RA patients producing autoantibodies. For rs7975232 SNP, we observed a significant association of the variant homozygous genotype with SLE ( = 0.009, OR = 1.82), pSS ( = 0.046, OR = 1.66), and RA ( = 0.028, OR = 1.75) susceptibility. Moreover, we reported associations of this genotype with clinical phenotypes of SLE and pSS. Lastly, the GG genotype of rs731236 was associated with a lower RA susceptibility ( = 0.045, OR = 0.55). Our results show that the explored VDR polymorphisms are significantly associated with autoimmune connective tissue disorders and support the hypothesis that the genetic variability of VDR gene may be involved in susceptibility to these diseases in Italian population.
维生素 D 是一种重要的激素,参与多种生理过程,其活性与维生素 D 受体(VDR)的结合有关。VDR 基因中的遗传多态性可以调节受体的表达或功能,从而改变维生素 D 的作用。VDR 基因的变体与许多对维生素 D 治疗敏感的疾病和自身免疫性疾病的易感性有关,但关于意大利人群自身免疫性结缔组织疾病,尚无相关数据。我们分析了 695 例自身免疫性结缔组织疾病患者(308 例系统性红斑狼疮(SLE)、195 例原发性干燥综合征(pSS)和 192 例类风湿关节炎(RA))和 246 例健康对照者的三个 VDR 多态性,旨在评估 VDR SNPs 与意大利人群这些疾病易感性的可能关联。通过等位基因鉴别分析对 VDR 基因中的 rs2228570、rs7975232 和 rs731236 进行基因分型。进行了病例对照关联研究和基因型表型相关性分析。我们发现 rs2228570 TT 基因型的 SLE 发病风险更高( = 0.029,OR = 1.79)。虽然这种变体在产生自身抗体的 RA 患者中明显较少,但我们没有观察到 pSS 或 RA 易感性与该 SNP 之间存在关联。对于 rs7975232 SNP,我们观察到该变体纯合基因型与 SLE( = 0.009,OR = 1.82)、pSS( = 0.046,OR = 1.66)和 RA( = 0.028,OR = 1.75)易感性显著相关。此外,我们报告了该基因型与 SLE 和 pSS 临床表型的关联。最后,rs731236 的 GG 基因型与较低的 RA 易感性相关( = 0.045,OR = 0.55)。我们的结果表明,所研究的 VDR 多态性与自身免疫性结缔组织疾病显著相关,支持 VDR 基因遗传变异性可能参与意大利人群这些疾病易感性的假说。