伊拉克类风湿性关节炎患者样本中 MTHFR 基因 rs1801133 和 rs1801131 多态性与甲氨蝶呤治疗药物不良反应的关系

Qassim Mahdi Mutlak, Ali Abdulhussain Kasim
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摘要

背景:甲氨蝶呤是治疗类风湿性关节炎(RA)的主要药物之一,具有广泛的药物不良反应,然而,药物不良反应与基因多态性之间的关系仍有待进一步研究,而且缺乏针对阿拉伯裔伊拉克人在这方面的研究。研究目的评估伊拉克 RA 患者 MTHFR 基因中 SNPs(rs1801133G>A 和 rs1801131T>G)基因突变与药物不良反应之间的关系。研究方法一项观察性研究,涉及 95 名已确诊的伊拉克 RA 患者。根据药物不良反应的发生情况对患者进行分类。采用聚合酶链式反应-限制性片段长度多态性(PCR-RFLP)检测 MTHFR 变体(rs1801133 和 rs1801131)。韩国 Macrogen 公司提供了冻干形式的正向和反向引物。所有 PCR 过程均使用 PCR 热循环仪(德国)进行。研究结果研究共纳入 95 例 RA 患者,平均年龄(43.1±10.6)岁,大多数患者为女性(85.3%),约 35.8%为吸烟者,大多数患者的疾病活动度较低(45.2%),其次为中度(41.1%)、高度(9.5%)和缓解(4.2%)。个别基因多态性与药物不良反应无明显关联。rs1801133的AG单倍型和rs1801131多态性与总体药物不良反应风险的降低有关,而rs1801133的GT单倍型和rs1801131多态性与药物不良反应风险的增加略有关联。结论总之,我们成功地找到了一组药物遗传学指标,它们在预测类风湿关节炎患者对甲氨蝶呤治疗的反应方面具有潜在价值。rs1801133 rs1801131 多态性的单倍型与降低或增加 MTX 药物不良反应的风险有关。因此,在开始治疗前对患者的单倍型进行评估非常重要,这样我们就能以最合适的剂量和最可耐受的剂量获得预期的治疗效果。
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Association of the rs1801133 and rs1801131 polymorphisms in the MTHFR gene and the adverse drug reaction of methotrexate treatment in a sample of Iraqi rheumatoid arthritis patients
Background: Methotrexate is one of the mainstays for treating rheumatoid arthritis (RA) with a wide range of adverse drug reactions, however, it’s the relationship between adverse drug reactions and genetic polymorphism remains to be highlighted, and there is a lack of studies concerning Arabic Iraqi population regarding this aspect. Objective: Evaluate the association between genetic mutations in the MTHFR gene in SNPs (rs1801133G>A and rs1801131T>G) on the adverse drug reaction for RA Iraqi patients. Methods: An observational study, that involved 95 Iraqi RA patients with established RA. Patients were divided according to the occurrence of adverse drug reactions. A polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was being utilized for MTHFR variants (rs1801133 and rs1801131). The Macrogen Company (Korea) provided the forward and reverse primers in lyophilized form. All PCR procedures are carried out using a PCR thermal cycler (Germany). Results: The study included 95 patients with RA, with a mean age of 43.1 ± 10.6 years, most of the patients were female (85.3%), about 35.8% were smokers, most of the patients had disease low activity (45.2%), followed by moderate (41.1%), high (9.5%), and remission (4.2%). No significant association between individual genetic polymorphism with adverse drug reactions. AG haplotype for rs1801133 rs1801131 polymorphism is associated with reducing the risk of overall adverse drug reactions, meanwhile, GT haplotype for rs1801133, and rs1801131 polymorphism were marginally associated with increased risk of adverse drug reactions. Conclusion: In conclusion, we have successfully found a panel of pharmacogenetic indicators that have the potential to be valuable in predicting the response to methotrexate treatment in patients with rheumatoid arthritis. Haplotypes for rs1801133 rs1801131 polymorphism are associated with reducing or increasing the risk of MTX adverse drug reactions. It is very important to evaluate patients’ haplotypes before starting the therapy program so that we can expect the treatment outcome with the most suitable dose and most tolerable one at the same time.
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