Department of Rheumatology, Flinders Medical Centre, Flinders University, South Australia, Australia.
Ann Pharmacother. 2013 Mar;47(3):e15. doi: 10.1345/aph.1R542. Epub 2013 Feb 27.
To study the pharmacokinetics and pharmacogenetics of leflunomide and document its efficacy and safety in the treatment of inflammatory arthritis in a patient with end-stage renal disease (ESRD) who was on peritoneal dialysis.
Therapy for a 78-year-old man with ESRD who required peritoneal dialysis was started with leflunomide 10 mg/day for psoriatic arthritis. The dosage was increased to 20 mg/day after 3 months. Monitoring was continued until the patient's unexpected death from myocardial infarction at 8 months. Total and unbound teriflunomide (the active metabolite of leflunomide) concentrations were measured by liquid-chromatography-tandem mass spectrometry. Genotyping for CYP2C19 and ABCG2 polymorphisms, both known to influence teriflunomide pharmacokinetics, was also performed.
Total concentrations of teriflunomide varied between 5.2 and 23.2 mg/L, while unbound concentrations varied between 0.0306 and 0.1468 mg/L. The unbound fraction varied between 0.367% and 0.71%. Teriflunomide was found in the dialysate at a concentration of 0.0981 mg/L. A single CYP2C19 loss of function allele was present, as was wild-type ABCG2. Leflunomide appeared to be therapeutically effective, as evidenced by a reduction in daily prednisolone dosage from 20 mg to 6mg; the Disease Activity Score in 28 joints (DAS28) was 5.46 at enrollment and 4.03 after 7 months. Health Assessment Questionnaire-Disability Index improved from 0.5 to 0.125 at 7 months. Numerous significant adverse events that were considered unrelated to leflunomide occurred.
Dose adjustment for leflunomide does not appear to be required in the context of ESRD requiring peritoneal dialysis. We present novel evidence that a small amount of teriflunomide is removed by peritoneal dialysis. This case suggests that leflunomide is safe to use as therapy for inflammatory arthritis despite the presence of ESRD requiring peritoneal dialysis.
研究来氟米特的药代动力学和药物遗传学,并记录其在接受腹膜透析的终末期肾病(ESRD)患者中治疗炎症性关节炎的疗效和安全性。
一位 78 岁男性患有 ESRD,需要腹膜透析,开始时给予来氟米特 10mg/天治疗银屑病关节炎。3 个月后,剂量增加至 20mg/天。监测一直持续到 8 个月时患者因心肌梗死意外死亡。通过液-质联用技术测定总游离特立氟胺(来氟米特的活性代谢物)浓度。还进行了 CYP2C19 和 ABCG2 多态性的基因分型,这两种多态性已知会影响特立氟胺的药代动力学。
特立氟胺的总浓度在 5.2 至 23.2mg/L 之间,而游离浓度在 0.0306 至 0.1468mg/L 之间。游离分数在 0.367%至 0.71%之间。特立氟胺在透析液中的浓度为 0.0981mg/L。存在单个 CYP2C19 失活功能等位基因,同时存在野生型 ABCG2。来氟米特似乎具有治疗效果,表现在每日泼尼松剂量从 20mg 减少到 6mg;入组时的 28 个关节疾病活动度评分(DAS28)为 5.46,7 个月后为 4.03。7 个月时健康评估问卷残疾指数从 0.5 改善至 0.125。发生了许多被认为与来氟米特无关的严重不良事件。
对于需要腹膜透析的 ESRD,来氟米特的剂量似乎不需要调整。我们提供了新的证据表明,少量的特立氟胺通过腹膜透析清除。该病例表明,尽管存在需要腹膜透析的 ESRD,来氟米特仍可安全用于治疗炎症性关节炎。