University of South Australia, Sansom Institute for Health Research & School of Pharmacy & Medical Sciences, Frome Road, GPO Box 2471, Adelaide, South Australia, 5000, Australia.
Pharmacogenomics. 2012 Sep;13(12):1427-34. doi: 10.2217/pgs.12.118.
Leflunomide is a disease-modifying antirheumatic drug used in the treatment of rheumatoid arthritis. Not all patients respond to leflunomide and, as it has potentially serious side effects, targeting only those most likely to benefit would address a clinical need. We aimed to determine whether variations in the gene encoding DHODH, the molecular target of leflunomide, might include biomarkers that could be used to rationalize provision of this drug.
MATERIALS & METHODS: We analyzed six haplotype-tagging SNPs in DHODH in 56 patients with rheumatoid arthritis treated with leflunomide. Clinical response was determined by assessing the change in 28 joint disease activity score over the first 3 months of treatment.
RESULTS & CONCLUSION: Carriage of a six-marker DHODH haplotype was associated with a reduced treatment response (p = 0.008). This suggests that a functional variant in strong linkage disequilibrium with this haplotype may predispose to reduced leflunomide efficacy.
来氟米特是一种用于治疗类风湿关节炎的疾病修饰抗风湿药物。并非所有患者对来氟米特都有反应,而且由于其具有潜在的严重副作用,因此仅针对最有可能受益的患者进行靶向治疗将满足临床需求。我们旨在确定编码来氟米特的分子靶标二氢乳清酸脱氢酶(DHODH)的基因变异是否可能包含可用于合理化提供该药物的生物标志物。
我们在 56 例接受来氟米特治疗的类风湿关节炎患者中分析了 DHODH 中的 6 个单倍型标记 SNP。通过评估治疗后 3 个月内 28 个关节疾病活动评分的变化来确定临床反应。
携带 6 个标记物 DHODH 单倍型与治疗反应降低相关(p=0.008)。这表明与该单倍型具有强连锁不平衡的功能性变体可能导致来氟米特疗效降低。