Glutathione S-transferase M1 and T1 gene polymorphisms in psoriasis patients: a pilot case-control study

IF 0.2 Q4 DERMATOLOGY
Noha Z Tawfik, Hoda Abdallah, Mona Abdullah, Hagar Alshaarawy, M. Atwa
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Abstract

Background The exact etiology of psoriasis remains unknown; nevertheless, it has been found that oxidative stress plays a vital role. Among the multiple antioxidant enzymes, genetic polymorphisms in the Glutathione S-Transferases (GSTs) led to an imbalance in the antioxidant system, resulting in increased levels of reactive oxygen species. Accordingly, the polymorphism in these genes could increase the susceptibility to psoriasis. Objectives To assess the association between Glutathione S-Transferase M1 (GSTM1) and Glutathione S Transferase Theta-1 (GSTT1) gene polymorphisms in psoriasis patients compared to healthy controls. Methods A total of 200 participants, 100 psoriasis cases who were assessed by the Psoriasis Area and Severity Index (PASI), and 100 healthy controls were included. DNA extraction was done followed by multiplex PCR to detect genetic polymorphism in the GSTM1 and GSTT1 genes, Finally, the relation between the presence of polymorphism and the severity of psoriasis was estimated. Results The null genotype frequency of GSTM1 and GSTT1 was 76.0% and 58.0%, respectively among psoriasis patients, while it was 58.0% and 55.0%, respectively among healthy controls. There was a significantly higher risk for psoriasis in patients with the null genotype GSTM1 (OR=2.293) as compared to controls. On the other hand, there was no statistically significant relation between their polymorphisms and family history, psoriasis severity, and PASI score. Conclusion The null genotype GSTM1 could increase the risk of psoriasis susceptibility especially among males.
银屑病患者谷胱甘肽s -转移酶M1和T1基因多态性:一项试点病例对照研究
背景银屑病的确切病因尚不清楚;然而,已经发现氧化应激起着至关重要的作用。在多种抗氧化酶中,谷胱甘肽S-转移酶(GSTs)的遗传多态性导致抗氧化系统失衡,导致活性氧水平升高。因此,这些基因的多态性可能会增加银屑病的易感性。目的与健康对照组相比,评估银屑病患者谷胱甘肽S转移酶M1(GSTM1)和谷胱甘肽S转移蛋白酶θ1(GSTT1)基因多态性之间的关系。方法共有200名参与者,100名银屑病患者通过银屑病面积和严重程度指数(PASI)进行评估,100名健康对照被纳入其中。通过DNA提取和多重PCR检测GSTM1和GSTT1基因的多态性。最后,估计多态性的存在与银屑病严重程度之间的关系。结果银屑病患者GSTM1和GSTT1的零基因型频率分别为76.0%和58.0%,健康对照组为58.0%和55.0%。与对照组相比,GSTM1基因型无效的患者患银屑病的风险显著更高(OR=2.293)。另一方面,它们的多态性与家族史、银屑病严重程度和PASI评分之间没有统计学上的显著关系。结论GSTM1基因型缺失可增加银屑病易感性,尤其是男性。
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