Samford University, Birmingham, AL, USA.
Ann Pharmacother. 2010 Sep;44(9):1422-9. doi: 10.1345/aph.1P218. Epub 2010 Aug 17.
To review the pharmacology, pharmacokinetics, efficacy, and safety of milnacipran and evaluate relevant clinical trial data.
MEDLINE, International Pharmaceutical Abstracts, and Google Scholar searches (1966-June 2010) were conducted using the key words fibromyalgia, milnacipran, and serotonin-norepinephrine reuptake inhibitor. Searches were limited to articles published in English.
All available English-language articles of human studies were evaluated. One pharmacokinetic study reviewed included animal data. References cited in identified articles were used for additional evaluation.
Milnacipran is a serotonin-norepinephrine reuptake inhibitor with a 3-fold increased selectivity for norepinephrine compared to serotonin. It is well absorbed with 85-90% bioavailability. Maximum concentrations are achieved 2-4 hours after administration. Milnacipran does not undergo cytochrome P450 metabolism and has a half-life of 6-8 hours. Fifty-five percent of each dose is excreted unchanged in the urine. Dose adjustment is needed in patients with an estimated creatinine clearance of <30 mL/min. Clinical trials indicated that twice-daily dosing at 100 mg/day or 200 mg/day was superior to single-daily dosing. Studies further established the effectiveness of both doses in the treatment of fibromyalgia pain utilizing patient self-reported pain scores, as well as on a visual analog scale, Patient Global Impression of Change scale, and the Short-Form 36 Physical Component Summary. A 6-month extension trial, which evaluated patients continued on milnacipran for up to 1 year, demonstrated continued pain relief. The most common adverse drug reaction associated with milnacipran was nausea, which was reduced with slow-dose titration and administration with food.
Milnacipran is an effective treatment option for patients with fibromyalgia. More head-to-head clinical trials are necessary to assess its ultimate place in therapy.
回顾米那普仑的药理学、药代动力学、疗效和安全性,并评估相关的临床试验数据。
使用关键词纤维肌痛、米那普仑和 5-羟色胺去甲肾上腺素再摄取抑制剂,对 MEDLINE、国际药学文摘和 Google Scholar 搜索(1966 年至 2010 年 6 月)进行了检索。检索仅限于英文发表的文章。
评估了所有可用的人类研究的英文文章。综述中包含了一项药代动力学研究,该研究包括动物数据。还使用了在确定的文章中引用的参考文献进行进一步评估。
米那普仑是一种 5-羟色胺去甲肾上腺素再摄取抑制剂,与 5-羟色胺相比,对去甲肾上腺素的选择性增加了 3 倍。它具有良好的吸收性,生物利用度为 85-90%。给药后 2-4 小时达到最大浓度。米那普仑不经过细胞色素 P450 代谢,半衰期为 6-8 小时。每次剂量的 55%以原形从尿液中排出。估计肌酐清除率<30mL/min 的患者需要调整剂量。临床试验表明,每日两次 100mg 或 200mg 剂量优于每日一次剂量。进一步的研究还证实了这两种剂量在治疗纤维肌痛疼痛方面的有效性,包括患者自我报告的疼痛评分、视觉模拟评分、患者总体变化印象量表和简明健康状况调查问卷 36 项简表的身体成分部分。一项为期 6 个月的扩展试验评估了继续使用米那普仑治疗长达 1 年的患者,结果表明疼痛持续缓解。与米那普仑相关的最常见药物不良反应是恶心,通过缓慢剂量滴定和与食物一起给药可以减少这种不良反应。
米那普仑是治疗纤维肌痛患者的有效治疗选择。需要更多的头对头临床试验来评估其在治疗中的最终地位。