Taşbaş Ozgür, Borman Pınar, Gürhan Karabulut Halil, Tükün Ajlan, Yorgancıoğlu Rezan
Ankara Training and Research Hospital I. Clinic of Physical Medicine and Rheumatology, Cebeci, Ankara, Turkey.
Open Rheumatol J. 2011;5:30-5. doi: 10.2174/1874312901105010030. Epub 2011 Oct 14.
The C677T and A1298C polymorphisms of methylenetatrahydrofolate reductase (MTHFR) gene are reported to have a relationship to methotrexate (MTX) metabolism, with conflicting results. The aim of this study was to determine the frequency of MTHFR C677 T and A1298C gene polymorphisms in a group of Turkish RA patients and evaluate its association with MTX toxicity.Sixty-four patients with RA and 31 control subjects with a mean age of 48.7 ±12.5 and 46.2 ± 13.4 years, were enrolled to the study. Demographic characteristics were obtained and MTX-related adverse effects were recorded in the patient group. The A1298C and C677T polymorphisms of the MTHFR gene were analyzed and the distribution of genotypes according side effects, were determined.The frequency of MTHFR C677T and A1298C polymorphisms were similar in the patient and control groups. Folic acid supplementation with a mean dose of 5mg folic acid/week, was present in all patients. Thirty-six of the 64 patients showed adverse effects to MTX treatment, and MTX had been discontinued in 12 (18.8%) patients due to side effects and/or inefficacy. MTHFR C677T and A1298C gene polymorphisms were found to be similar in patients with and without MTX-related adverse events.In conclusion, A1298C and C677T polymorphisms in the MTHFR gene, were not related with MTX-related toxicity in RA patients receiving folate supplementation. Further studies are needed to illuminate the polymorphisms in other enzymes that might be responsible from the MTX toxicity in patients suffering from RA.
据报道,亚甲基四氢叶酸还原酶(MTHFR)基因的C677T和A1298C多态性与甲氨蝶呤(MTX)代谢有关,但结果相互矛盾。本研究的目的是确定一组土耳其类风湿关节炎(RA)患者中MTHFR C677T和A1298C基因多态性的频率,并评估其与MTX毒性的关联。64例RA患者和31例对照受试者纳入本研究,患者组平均年龄为48.7±12.5岁,对照组平均年龄为46.2±13.4岁。获取人口统计学特征,并记录患者组中与MTX相关的不良反应。分析MTHFR基因的A1298C和C677T多态性,并根据副作用确定基因型分布。患者组和对照组中MTHFR C677T和A1298C多态性的频率相似。所有患者均补充了平均剂量为5mg叶酸/周的叶酸。64例患者中有36例对MTX治疗有不良反应,12例(18.8%)患者因副作用和/或无效而停用MTX。在有和没有MTX相关不良事件的患者中,发现MTHFR C677T和A1298C基因多态性相似。总之,在接受叶酸补充的RA患者中,MTHFR基因的A1298C和C677T多态性与MTX相关毒性无关。需要进一步研究以阐明可能导致RA患者MTX毒性的其他酶的多态性。