Department of Internal Medicine, Arthritis and Autoimmunity Research Center, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, Daegu, 705-718, Republic of Korea.
Rheumatol Int. 2012 Jun;32(6):1837-42. doi: 10.1007/s00296-011-1989-5. Epub 2011 Jul 21.
We investigated associations between the methylenetetrahydrofolate reductase (MTHFR) polymorphisms C677T and A1298C and methotrexate (MTX)-related toxicities in Korean patients with rheumatoid arthritis (RA) taking MTX. One hundred sixty-seven patients with RA were enrolled in a cross-sectional study and genotyped for the single-nucleotide polymorphisms C677T and A1298C in MTHFR. Alleles, genotypes, and haplotypes of the C677T and A1298C polymorphisms were not associated with specific MTX toxicities. However, among RA patients with the 1298CC genotype, the proportion who experienced at least one toxicity was significantly greater than the proportion of patients with 1298AA who did (P = 0.043). In addition, the proportion of patients with the 677C/1298A haplotype who experienced toxicity was greater than the proportion of those with 677C/1298C who did (P = 0.032, odds ratio = 2.085, 95% confidence interval 1.058-4.106). In this study, MTHFR polymorphisms were associated with MTX toxicities in Korean patients with RA. Further study for association of MTHFR polymorphisms with MTX toxicities should be needed in larger RA population.
我们研究了亚甲基四氢叶酸还原酶(MTHFR)C677T 和 A1298C 多态性与接受甲氨蝶呤(MTX)治疗的韩国类风湿关节炎(RA)患者 MTX 相关毒性之间的关联。我们对 167 例接受 MTX 治疗的 RA 患者进行了一项横断面研究,并对 MTHFR 中的单核苷酸多态性 C677T 和 A1298C 进行了基因分型。C677T 和 A1298C 多态性的等位基因、基因型和单倍型与特定的 MTX 毒性无关。然而,在 1298CC 基因型的 RA 患者中,至少发生一种毒性的患者比例明显高于 1298AA 基因型的患者(P = 0.043)。此外,发生毒性的 677C/1298A 单倍型患者比例大于发生毒性的 677C/1298C 单倍型患者比例(P = 0.032,比值比= 2.085,95%置信区间 1.058-4.106)。在这项研究中,MTHFR 多态性与韩国 RA 患者的 MTX 毒性相关。在更大的 RA 人群中,需要进一步研究 MTHFR 多态性与 MTX 毒性的关联。