Polymorphism rs10499194 of the TNFA1P3 gene is not associated with a predisposition to ankylosing spondylitis in the Russian cohort of patients

M. Krylov, S. Erdes, N. Konovalova, D. Varlamov
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Abstract

Background. Recently, numerous studies have shown that TNFAIP3 gene polymorphisms have been associated with susceptibility to certain autoimmune inflammatory diseases, including systemic lupus erythematosus, scleroderma, rheumatoid arthritis and psoriasis. However, the results of studies devoted to the study of associations between TNFAIP3 gene polymorphisms and the risk of ankylosing spondylitis (AS) are ambiguous and few.The aim of the study was to study the possible association of hs10499194 polymorphism of the TNFAIP3 gene with a predisposition to AS and its clinical phenotypes.Material and methods. The rs10499194 S/T polymorphism of the TNFA1P3 gene was studied in two hundred patients with AS (130 men and 70 women). All patients were diagnosed with AS, according to the modified New York criteria, 1984 and high activity of the disease. Demographic and clinical-serological characteristics were studied in all patients. The average age of patients was 39.4±12.6 years; the average duration of the disease was 15.0±10.6 years. Out of 200 patients, 175 (87.5%) were seropositive for HLA-B27 antigen. Extra axial arthritis was detected in 125 (62.5%) patients, 148 (74.0%) had enthesitis, 137 (68.5%) had coxitis. The polymorphism rs10499194 of the TNFAIP3 gene was studied using an allelespecific polymerase chain reaction in real time (PCR-RV) using the Synthol kit.Results. The analysis of the frequencies of genotypes and alleles did not show significant differences with the control group. Stratification by sex, age, and clinical manifestations showed an association of the CT genotype with an increased risk of AS among men (OR=2.24; p=0.010), the TT genotype and the T allele with a high risk of predisposition to the development of extra axillary peripheral arthritis (OR=3.94; p=0.019 and OR=1.64; p=0.027 respectively). The BASDAI index was statistically significantly higher in carriers of the TT genotype compared to the CT genotype (p=0.002).Conclusion. The present study confirmed the association of the genetic polymorphism rs10499194 of the TNFAIP3 gene with AS. Stratification by gender and clinical manifestations showed an association of the CT genotype with an increased risk of AS among men, the TT genotype and the T allele with a high risk of predisposition to the development of extra axillary peripheral arthritis and a high BASDAI index in carriers of the TT genotype.
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在俄罗斯队列患者中,TNFA1P3基因多态性rs10499194与强直性脊柱炎易感性无关
背景。近年来,大量研究表明,TNFAIP3基因多态性与某些自身免疫性炎症疾病的易感性相关,包括系统性红斑狼疮、硬皮病、类风湿性关节炎和牛皮癣。然而,致力于研究TNFAIP3基因多态性与强直性脊柱炎(AS)风险之间关系的研究结果是模糊的,而且很少。本研究的目的是研究TNFAIP3基因hs10499194多态性与AS易感性及其临床表型的可能关联。材料和方法。在200名AS患者(130名男性和70名女性)中研究了TNFA1P3基因的rs10499194 S/T多态性。根据1984年修订的纽约标准,所有患者均被诊断为AS,并伴有高活动性疾病。研究了所有患者的人口学和临床血清学特征。患者平均年龄39.4±12.6岁;平均病程15.0±10.6年。200例患者中,175例(87.5%)血清HLA-B27抗原阳性。125例(62.5%)患者有轴外关节炎,148例(74.0%)有膝炎,137例(68.5%)有膝炎。采用Synthol试剂盒,采用等位基因特异性聚合酶链反应(PCR-RV)对TNFAIP3基因rs10499194的多态性进行了研究。基因型和等位基因频率分析与对照组无显著差异。性别、年龄和临床表现分层显示,男性中CT基因型与AS风险增加相关(OR=2.24;p=0.010), TT基因型和T等位基因易患腋下外周性关节炎(OR=3.94;p=0.019, OR=1.64;p = 0.027)。TT基因型携带者的BASDAI指数高于CT基因型携带者(p=0.002)。本研究证实了TNFAIP3基因的遗传多态性rs10499194与AS的相关性。性别和临床表现分层显示,CT基因型与男性患AS的风险增加有关,TT基因型和T等位基因与腋下外周性关节炎的高风险相关,TT基因型携带者的BASDAI指数较高。
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