复发性风湿病患者TNFAIP3、PTPN22、IRF5和IL-10基因多态性的分子分析

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Aynaz Asgharvand-Hajeb, Sima Shahmohammadi-Farid, Maryam Saberivand, Azam Safary, Kamran Javidi-Aghdam, Raha Khabbazi, Alireza Khabbazi
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引用次数: 0

摘要

目的:复发性风湿病(PR)的特点是关节和关节周围结构的疼痛和肿胀频繁和不规则发作。在这项研究中,我们研究了PR患者中TNFAIP3、PTPN22、IRF5和IL-10基因的单核苷酸多态性(snp)。方法:在一项横断面研究中,招募了诊断为PR的患者和两组对照组,包括类风湿关节炎(RA)患者和健康对照组(hc)。所有参加者都是阿塞拜疆人。对TNFAIP3 (rs2230926、rs5029937)、PTPN22 (rs1217407、rs1217413)、IRF5 (rs10954213、rs2004640)和IL-10 (rs1800872、rs1800896)基因snp进行基因分型。结果:25例PR患者、41例RA患者和40例hc患者共检测到8个snp基因型。与RA和HC组相比,PR组中TNFAIP3 rs2230926的TT基因型多态性和IL10 rs1800872的GG基因型多态性较少。与RA和HC组相比,PR组中TNFAIP3 rs2230926多态性的C等位基因更为常见。与hc相比,PR组中IL10 rs1800896的TC基因型和C等位基因多态性以及IRF5 rs10954213的AG基因型多态性更为常见;然而,PR组和RA组之间没有显著差异。两组间TNFAIP3 rs5025937、IRF5 rs2004640、PTPN22 rs1217413、PTPN22 rs1217407基因型及等位基因的分布无显著差异。结论:Azeri人群携带TNFAIP3 rs2230926、CC和TC基因型C等位基因多态性、IL10 rs1800896基因型C等位基因多态性、IRF5 rs10954213基因型AG基因型多态性与PR相关。•TNFAIP3 rs2230926多态性的TT基因型在复发性风湿病患者中比在类风湿关节炎患者和健康个体中更少见。•IL10 rs1800872多态性的GG基因型在复发性风湿病患者中比在类风湿关节炎患者和健康个体中更少见。•CC和TC基因型、IL10 rs1800896的C等位基因、IRF5 rs10954213多态性的AG基因型在复发性风湿病患者中比健康人更常见,但在复发性风湿病和类风湿关节炎患者中无差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular analysis of TNFAIP3, PTPN22, IRF5, and IL-10 gene polymorphisms in palindromic rheumatism.

Objective: Palindromic rheumatism (PR) is characterized by frequent and irregular attacks of pain and swelling in the joints and peri-articular structures. In this study, we investigated TNFAIP3, PTPN22, IRF5, and IL-10 genes' single-nucleotide polymorphisms (SNPs) in patients with PR.

Methods: In a cross-sectional study, patients with a diagnosis of PR and two control groups, including rheumatoid arthritis (RA) patients and healthy controls (HCs), were recruited. All participants were Azeri. The TNFAIP3 (rs2230926, rs5029937), PTPN22 (rs1217407, rs1217413), IRF5 (rs10954213, rs2004640), and IL-10 (rs1800872, rs1800896) gene SNPs were genotyped.

Results: Eight SNPs were genotyped in 25 PR patients, 41 RA patients, and 40 HCs. The TT genotype of TNFAIP3 rs2230926 and GG genotype of IL10 rs1800872 polymorphisms were less common in the PR group compared to the RA and HC groups. The C allele of TNFAIP3 rs2230926 polymorphism was more common in the PR group compared to the RA and HC groups. The TC genotype and C allele of IL10 rs1800896 and AG genotype of IRF5 rs10954213 polymorphisms were more common in the PR group compared to the HCs; however, there were no significant differences between the PR and RA groups. No significant difference was observed in the distribution of TNFAIP3 rs5025937, IRF5 rs2004640, PTPN22 rs1217413, and PTPN22 rs1217407 genotypes and alleles between the studied groups.

Conclusions: Carrying C allele of TNFAIP3 rs2230926, CC and TC genotypes and C allele of IL10 rs1800896, and AG genotype of IRF5 rs10954213 polymorphisms are associated with PR in the Azeri population. Key Points • The TT genotype of the TNFAIP3 rs2230926 polymorphism is less common in patients with palindromic rheumatism than in patients with rheumatoid arthritis and healthy individuals. • The GG genotype of the IL10 rs1800872 polymorphism is less common in patients with palindromic rheumatism than in patients with rheumatoid arthritis and healthy individuals. • The CC and TC genotypes, C allele of IL10 rs1800896, and AG genotype of IRF5 rs10954213 polymorphism are more common in patients with palindromic rheumatism than in healthy individuals, but there is no difference between patients with palindromic rheumatism and rheumatoid arthritis.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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