Il17A (rs2275913 G>A) and IL17F (rs2397084 T>C) gene polymorphisms: relation to psoriasis risk and response to methotrexate

Ashraf M. Hamza, R. A. Abo Elwafa, N. Ramadan, S. Omar
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引用次数: 1

Abstract

Background IL17F rs763780 polymorphism results in substitution of histidine to arginine at amino acid 161, leading to upregulation of IL17F and increased propensity to autoimmune diseases. The single nucleotide polymorphism rs2275913 (G197A) involves a substitution of the guanine by an adenine nucleotide base in IL17A gene promotor which plays a key role in regulation of cytokine transcription. The relation of IL17 polymorphisms however to psoriasis risk and response to methotrexate has not been previously studied in Egyptians. Objective To study the relation of IL17A (rs2275913 G>A) and IL17F (rs2397084 T>C) polymorphisms to psoriasis risk and assess their predictive role regarding response to methotrexate. Patients and methods The study was conducted in two phases. First, a case–control study including 100 patients with chronic plaque psoriasis and 100 healthy control patients was conducted for IL17A (rs2275913) and IL17F (rs2397084) polymorphisms by real-time PCR. Second, a cohort study was adopted where the patients with psoriasis were treated with methotrexate weekly intramuscularly (0.6 mg/kg) for 12 weeks and followed for clinical response. Results IL17F TT genotype was more frequent in patients (87%) than controls (68%), whereas TC genotype was more frequent in controls (32%) than patients (13%). TT genotype was associated with increased risk of psoriasis, whereas the TC allele was associated with a decreased risk. There was no significant difference regarding IL17A GG, GA, and AA genotype frequencies between patients and controls. Psoriasis area and severity index greater than or equal to 75% was achieved in 22 patients (73.3%) with the TT genotype and eight patients (26.7%) with TC genotype (P=0.019). Conclusion IL17F (rs2397084 T>C) TT genotype could be considered a susceptibility marker in Egyptian patients. Psoriatic patients with TT genotype and T allele of IL17F (rs2397084 T>C) are likely to show a better response to methotrexate.
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Il17A(rs2275913 G>A)和IL17F(rs2397084 T>C)基因多态性与银屑病风险和甲氨蝶呤反应的关系
背景IL17F rs763780多态性导致氨基酸161处组氨酸被精氨酸取代,导致IL17F上调并增加自身免疫性疾病的倾向。单核苷酸多态性rs2275913(G197A)涉及IL17A基因启动子中的腺嘌呤核苷酸碱基取代鸟嘌呤,其在细胞因子转录调控中起关键作用。然而,IL17多态性与银屑病风险和甲氨蝶呤反应的关系此前尚未在埃及人中进行研究。目的研究IL17A(rs2275913 G>A)和IL17F(rs2397084 T>C)多态性与银屑病风险的关系,并评估其对甲氨蝶呤反应的预测作用。患者和方法本研究分两个阶段进行。首先,通过实时PCR对IL17A(rs2275913)和IL17F(rs2397084)多态性进行了一项包括100名慢性斑块型银屑病患者和100名健康对照患者的病例对照研究。其次,采用了一项队列研究,银屑病患者每周肌肉注射甲氨蝶呤(0.6 mg/kg)治疗12周,并随访临床反应。结果IL17F TT基因型在患者中(87%)比对照组(68%)更常见,而TC基因型在对照组中(32%)比患者(13%)更常见。TT基因型与银屑病风险增加相关,而TC等位基因与银屑病风险降低相关。IL17A-GG、GA和AA基因型频率在患者和对照组之间没有显著差异。结论IL17F(rs2397084T>C)TT基因型可作为埃及银屑病患者的易感标志。具有IL17F TT基因型和T等位基因(rs2397084T>C)的银屑病患者可能对甲氨蝶呤表现出更好的反应。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
0
审稿时长
17 weeks
期刊介绍: The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.
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