Association of MTHF 677TT with adverse drug reactions and RFC G80A with non-response and adverse drug reactions in methotrexate therapy

Manahel Mahmood AlSabbagh
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Abstract

Being an anti-metabolite and anti-inflammatory agent, Methotrexate, a folate analogue, is indicated for a wide spectrum of diseases including moderate to severe chronic inflammatory disorders like psoriasis and rheumatoid arthritis and malignant diseases such as childhood acute lymphoblastic leukaemia and choriocarcinoma. The outcome of Methotrexate treatment varies. Though up to 50% of patients with inflammatory disorders show a favourable response; one third discontinues Methotrexate due to adverse drug reactions or non-response. Such diversity suggests an inter-individual variation due to multiple factors including genetic polymorphisms. This review was conducted to identify genotypes predictive of Methotrexate treatment outcome. More than 15 alleles located in eight genes were explored by over 25 studies. Among those, we identified MTHFrs1801133TT genotype to be likely associated with adverse drug reactions and RFCrs1051266A allele to be associated with both, non-response and adverse drug reactions. We recommend the conduction of meta-analysis to verify these findings.

甲氨蝶呤治疗中MTHF 677TT与药物不良反应、RFC G80A与无反应及药物不良反应的关系
作为一种抗代谢物和抗炎剂,叶酸类似物甲氨蝶呤被用于广泛的疾病,包括中度至重度慢性炎症性疾病,如牛皮癣和类风湿关节炎,以及恶性疾病,如儿童急性淋巴细胞白血病和绒毛膜癌。甲氨蝶呤治疗的结果各不相同。尽管高达50%的炎症性疾病患者表现出良好的反应;三分之一的患者因药物不良反应或无反应而停用甲氨蝶呤。这种多样性表明个体间的差异是由包括遗传多态性在内的多种因素引起的。本综述旨在确定预测甲氨蝶呤治疗结果的基因型。超过25项研究发现了8个基因中的15个以上等位基因。其中,我们发现MTHFrs1801133TT基因型可能与药物不良反应相关,RFCrs1051266A等位基因型可能与无反应和药物不良反应相关。我们建议进行荟萃分析来验证这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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