Department of Experimental Medicine and Oncology, University of Turin, Italy.
Dis Markers. 2009;27(5):217-23. doi: 10.3233/DMA-2009-0666.
Immune and inflammatory response activation is a common feature of connective tissue diseases and systemic vasculitis. The aim of our study was to evaluate the possible involvement of TNFalpha c.-308A > G, IL-10 c.-1082A > G, uteroglobin c.38A > G, TGFbeta 1 c.869C > T and NFkappaB2 c.-1837T > C gene polymorphisms in susceptibility to connective tissue diseases. Our study cohort included 68 unrelated patients affected by rheumatoid arthritis (RA) (37 patients) and ANCA-positive [micropolyangiitis (mPA) 17 patients] or ANCA-negative systemic vasculitis [including 8 patients with Henoch-Schönlein purpura (HSP) and 6 patients with mixed cryoglobulinaemia (MC)] as well as 98 control subjects. Allele frequency analysis of uteroglobin c.38G > A polymorphism showed a significant increase in the c.38A allele in patients (p= 0.002). Genotype frequency analysis of uteroglobin and NF-kappaB2 gene polymorphisms in patients showed an increase in c.38GA and c.38AA genotypes in the uteroglobin gene (p=0.02) coupled with an increase in homozygous c.-1837CC in the NF-kappaB2 gene (p=0.02). Our data suggest that genetic variation in UG and NF-kappaB2 pathways could have effects in connective tissue disease susceptibility.
免疫和炎症反应的激活是结缔组织疾病和系统性血管炎的共同特征。我们的研究目的是评估 TNFalpha c.-308A > G、IL-10 c.-1082A > G、uteroglobin c.38A > G、TGFbeta 1 c.869C > T 和 NFkappaB2 c.-1837T > C 基因多态性与结缔组织疾病易感性的可能相关性。我们的研究队列包括 68 名无亲缘关系的患者,其中包括类风湿关节炎(RA)(37 名患者)和 ANCA 阳性(微动脉炎(mPA)17 名患者)或 ANCA 阴性系统性血管炎[包括 8 名过敏性紫癜(HSP)患者和 6 名混合性冷球蛋白血症(MC)患者]以及 98 名对照者。uteroglobin c.38G > A 多态性的等位基因频率分析显示,患者中 c.38A 等位基因的频率显著增加(p=0.002)。患者中 uteroglobin 和 NF-kappaB2 基因多态性的基因型频率分析显示,uteroglobin 基因中 c.38GA 和 c.38AA 基因型的增加(p=0.02),同时 NF-kappaB2 基因中 c.-1837CC 纯合子的增加(p=0.02)。我们的数据表明,UG 和 NF-kappaB2 通路的遗传变异可能对结缔组织疾病的易感性有影响。