NLRP3(rs10754558)基因多态性和肿瘤坏死因子α可预测银屑病的疾病活动以及对甲氨蝶呤和阿达木单抗的反应。

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Fatma Z Kamel, Heba Allah Mohamed Hoseiny, Aya A El Shahawy, Ghada Boghdadi, Alia A El Shahawy
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引用次数: 0

摘要

背景:银屑病的全球发病率为 1-3%,不同种族和地理区域的发病率存在差异。疾病易感性和对抗肿瘤坏死因子-α(TNFα)药物的反应表明存在不同的遗传调节机制,其中可能包括 NLR 家族含吡咯啉结构域 3(NLRP3)多态性。评估银屑病患者的 NLRP3 基因多态性、血清 CRP 和 TNFα 水平,并评估 NLRP3 (rs10754558) 基因多态性、CRP 和 TNFα 与疾病严重程度的关系,以及它们作为生物标志物在银屑病患者对甲氨蝶呤和阿达木单抗反应中的作用。该研究共有 75 名被诊断为寻常型银屑病的患者,他们与由 75 名健康人组成的对照组进行了比较:结果:银屑病患者和对照组的 NLRP3 基因型和等位基因分布存在非常明显的差异(P = 0.002,0.004)。杂合子基因型 GC(OR = 3.67,95%CI:1.75-7.68,P = 0.0006)与银屑病风险增加有关。此外,GC 基因型与牛皮癣治疗无反应显著相关(OR = 11.7,95%CI:3.24-42.28,P = 0.0002)。在血清 CRP 和 TNFα 水平方面,银屑病患者与对照组之间的差异具有高度统计学意义(P 结论):NLRP3(rs10754558)基因型 GC 与严重银屑病和对银屑病药物无反应有关。因此,NLRP3(rs10754558)基因多态性是银屑病患者重要的预后生物标志物。血清 TNFα 可用于预测银屑病患者对治疗的反应。仍需开展更多研究,以评估 NLRP3 基因多态性在银屑病相关遗传风险和治疗结果中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NLRP3 (rs10754558) gene polymorphism and tumor necrosis factor alpha as predictors for disease activity and response to methotrexate and adalimumab in psoriasis.

Background: Psoriasis has a global prevalence of 1-3%, with variations observed across different ethnic groups and geographical areas. Disease susceptibility and response to anti-tumor necrosis factor-α (TNFα) drugs suggest different genetic regulatory mechanisms which may include NLR family pyrin domain containing 3 (NLRP3) polymorphism. Evaluation of the NLRP3 gene polymorphism, the serum level of CRP and TNFα in psoriasis patients and assessment of the NLRP3 (rs10754558) gene polymorphism, CRP and TNFα with disease severity and their role as biomarkers for response to Methotrexate and Adalimumab in psoriasis. The study had a total of 75 patients diagnosed with psoriasis vulgaris, who were compared to a control group of 75 healthy individuals.

Results: There was a highly significant difference in NLRP3 genotypes and alleles distribution between psoriasis patients and controls (P = 0.002,0.004). The heterozygote genotype GC (OR = 3.67,95%CI:1.75-7.68, P = 0.0006), was linked with increased risk of psoriasis. Additionally, The GC genotype was significantly associated with nonresponse to psoriasis therapy (OR = 11.7,95%CI:3.24-42.28, P = 0.0002). Regarding serum CRP and TNFα levels, there was a highly statistically significant difference between psoriasis patients and controls (P < 0.0001), and there was also a highly statistically significant difference between responders and non-responders in psoriasis patients regarding PASI 50 (P < 0.0001).

Conclusions: The NLRP3 (rs10754558) genotypes GC was associated with the severe form of psoriasis and with nonresponse to psoriasis medication. Therefore, NLRP3 (rs10754558) gene polymorphism is an important prognostic biomarker in psoriasis patients. The serum TNFα can be used as a predictor for response to therapy in psoriasis patients. More research for evaluation of role of the NLRP3 gene polymorphism in the genetic risks and treatment outcomes associated with psoriasis is still required.

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来源期刊
BMC Immunology
BMC Immunology 医学-免疫学
CiteScore
5.50
自引率
0.00%
发文量
54
审稿时长
1 months
期刊介绍: BMC Immunology is an open access journal publishing original peer-reviewed research articles in molecular, cellular, tissue-level, organismal, functional, and developmental aspects of the immune system as well as clinical studies and animal models of human diseases.
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