首页> 外文期刊>European journal of human genetics: EJHG >Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma.
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Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma.

机译:PTPN22单核苷酸多态性与类风湿关节炎相关,但与过敏性哮喘无关。

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摘要

PTPN22 gene encodes a lymphoid tyrosine phosphatase (LYP), an important negative regulator of T-cell responses. The 1858C>T (Arg620Trp) single nucleotide polymorphism (rs2476601) was found associated with autoimmune diseases, including rheumatoid arthritis (RA). Allergic diseases are similar to autoimmune diseases, by an exaggerated immune response to an antigen (allergen in this case) normally not invoking such response in healthy individuals. We investigated whether polymorphism 1858C>T in PTPN22 gene is associated with susceptibility to allergic asthma and RA in a Polish population. PTPN22 was genotyped in 173 patients with RA, in 198 patients with allergic asthma, and in 543 controls using PCR-RFLP. The patients with RA differed from healthy controls in frequencies of PTPN22 1858C>T alleles (P=0.0004; odds ratio (OR), 1.8; 95% CI, 1.33-2.55) and genotypes (P=0.0009). Strong associations of 1858T allele with RA limited to joints (0.21 vs 0.12, P=0.0002; OR, 2.1; 95% CI, 1.44-3.00), with erosive disease (0.20 vs 0.12, P=0.0003; OR, 1.92; 95% CI, 1.34-2.71), with a lack of rheumatoid factor (RF; 0.23 vs 0.12, P=0.0008; OR, 2.29; 95% CI, 1.44-3.63), and weak association with the presence of RF (0.17 vs 0.12, P=0.02; OR, 1.6; 95% CI, 1.10-2.40) in comparison with healthy controls were observed. Very strong association of 1858T allele (P<0.0001; OR, 2.72; 95% CI, 1.9-3.9) and T phenotype (P<0001; OR, 3.2; 95% CI, 2.1-4.9) with antibodies to cyclic citrullinated peptide (CCP) was found. When patients with allergic asthma were typed for PTPN22 1858C>T polymorphism, no difference with control was found. Subdivision of patients into those with mild, moderate, or severe asthma did not reveal any associations. In conclusion, we confirmed associations between several clinical manifestations of RA and PTPN22 1858T allele. However, no association with 1858C>T polymorphism was found for susceptibility to allergic asthma or for severity of the disease.
机译:PTPN22基因编码淋巴酪氨酸磷酸酶(LYP),T细胞反应的重要负调节剂。发现1858C> T(Arg620Trp)单核苷酸多态性(rs2476601)与自身免疫疾病有关,包括类风湿关节炎(RA)。过敏性疾病与自身免疫性疾病相似,其原因是对抗原(在这种情况下为过敏原)的免疫反应过度,在健康个体中通常不会引起这种反应。我们调查了PTPN22基因中的1858C> T多态性是否与波兰人群中过敏性哮喘和RA的易感性相关。使用PCR-RFLP在173例RA患者,198例过敏性哮喘患者和543例对照中对PTPN22进行了基因分型。 RA患者与PTPN22 1858C> T等位基因(P = 0.0004;比值比(OR),1.8; 95%CI,1.33-2.55)和基因型(P = 0.0009)的频率与健康对照组不同。 1858T等位基因与RA的强关联仅限于关节(0.21 vs 0.12,P = 0.0002; OR,2.1; 95%CI,1.44-3.00),与糜烂性疾病(0.20 vs 0.12,P = 0.0003; OR,1.92; 95% CI,1.34-2.71),没有类风湿因子(RF; 0.23 vs 0.12,P = 0.0008; OR,2.29; 95%CI,1.44-3.63),与RF的存在相关性较弱(0.17 vs 0.12,与健康对照组相比,观察到P = 0.02; OR,1.6; 95%CI,1.10-2.40)。 1858T等位基因(P <0.0001; OR,2.72; 95%CI,1.9-3.9)和T表型(P <0001; OR,3.2; 95%CI,2.1-4.9)与环状瓜氨酸化肽抗体( CCP)。当为过敏性哮喘患者输入PTPN22 1858C> T多态性时,与对照组无差异。将患者细分为轻度,中度或重度哮喘患者没有任何相关性。总之,我们证实了RA和PTPN22 1858T等位基因的几种临床表现之间的关联。然而,对于过敏性哮喘的易感性或疾病的严重性,没有发现与1858C> T多态性相关。

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