Piotrowski Piotr, Lianeri Margarita, Prokop Edyta, Wudarski Mariusz, Olesińska Marzena, Jagodziński Paweł P
Department of Biochemistry and Molecular Biology, Poznań University of Medical Sciences , Poznan , Poland.
Mod Rheumatol. 2014 Mar;24(2):296-9. doi: 10.3109/14397595.2013.854066.
The Fcrl3 -169T>C (rs7528684) polymorphism has been shown to be a risk factor of various autoimmune diseases, including systemic lupus erythematosus (SLE); however, these results are inconsistent between distinct ethnicities.
Using PCR-RFLP we studied the distribution of the FCRL3 -169T>C polymorphism in SLE patients (n = 263) and controls (n = 528) in a sample from the Polish population.
We found no significant differences of FCRL3 -169T>C genotypes and alleles between patients with SLE and healthy individuals. However, in the dominant model we found a significant association between the FCRL3 -169T>C polymorphism and the presence of anti-Scl-70 antibody (Ab) [OR = 4.747 (95 % CI = 1.639-13.749), p = 0.0011, p corr = 0.0198]. Moreover, in the dominant model we observed a significant contribution of FCRL3 -169T>C to the presence of either anti-La or anti-Scl-70 Abs [OR = 4.378 (95 % CI = 1.793-10.690, p = 0.0003, p corr = 0.0054)].
Our study demonstrated that the FCRL3 -169T>C polymorphism is not a risk factor of SLE in the Polish population, but this polymorphism may contribute to autoantibody production in this disease.
Fcrl3 -169T>C(rs7528684)多态性已被证明是包括系统性红斑狼疮(SLE)在内的多种自身免疫性疾病的危险因素;然而,不同种族之间的这些结果并不一致。
我们使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)研究了波兰人群样本中SLE患者(n = 263)和对照组(n = 528)中FCRL3 -169T>C多态性的分布。
我们发现SLE患者与健康个体之间FCRL3 -169T>C基因型和等位基因无显著差异。然而,在显性模型中,我们发现FCRL3 -169T>C多态性与抗Scl-70抗体(Ab)的存在之间存在显著关联[比值比(OR)= 4.747(95%置信区间(CI)= 1.639 - 13.749),p = 0.0011,校正p值(p corr)= 0.0198]。此外,在显性模型中,我们观察到FCRL3 -169T>C对抗La或抗Scl-70抗体的存在有显著贡献[OR = 4.378(95% CI = 1.793 - 10.690,p = 0.0003,p corr = 0.0054)]。
我们的研究表明,FCRL3 -169T>C多态性不是波兰人群中SLE的危险因素,但这种多态性可能在该疾病的自身抗体产生中起作用。