Rascol Olivier, Zesiewicz Theresa, Chaudhuri K Ray, Asgharnejad Mahnaz, Surmann Erwin, Dohin Elisabeth, Nilius Sigrid, Bauer Lars
Clinical Investigation Center CIC1436 and Department of Clinical Pharmacology and Neurosciences, INSERM, Toulouse University Hospital and University of Toulouse, Toulouse, France.
University of South Florida Ataxia Research Center, The Frances J. Zesiewicz Foundation for Parkinson's Disease at USF, Parkinson's Disease and Movement Disorders Clinic at the PADREC, James A. Haley Veterans' Administration, Tampa, FL, USA.
J Clin Pharmacol. 2016 Jul;56(7):852-61. doi: 10.1002/jcph.678. Epub 2015 Dec 31.
Pain is a troublesome nonmotor symptom of Parkinson's disease (PD). This double-blind exploratory pilot study (NCT01744496) was the first to specifically investigate the effect of a dopamine agonist on PD-associated pain as primary outcome. Patients with advanced PD (ie, receiving levodopa) and at least moderate PD-associated chronic pain (≥3 months, ≥4 points on 11-point Likert pain scale) were randomized to rotigotine (optimal/maximum dose ≤16 mg/24h) or placebo and maintained for 12 weeks. Primary efficacy variable was change in pain severity (Likert pain scale) from baseline to end of maintenance. Secondary variables included percentage of responders (≥2-point Likert pain scale reduction), King's PD Pain Scale (KPPS) domains, and PD Questionnaire (PDQ-8). Statistical analyses were exploratory. Of 68 randomized patients, 60 (rotigotine, 30; placebo, 30) were evaluable for efficacy. A numerical improvement in pain was observed in favor of rotigotine (Likert pain scale: least-squares mean [95%CI] treatment difference, -0.76 [-1.87 to 0.34]; P = .172), and proportion of responders was 18/30 (60%) rotigotine vs 14/30 (47%) placebo. An ∼2-fold numerical improvement in KPPS domain "fluctuation-related pain" was observed with rotigotine vs placebo. Rotigotine improved PDQ-8 vs placebo (-8.01 [-15.56 to -0.46]; P = .038). These results suggest rotigotine may improve PD-associated pain; a large-scale confirmatory study is needed.
疼痛是帕金森病(PD)中一种棘手的非运动症状。这项双盲探索性试点研究(NCT01744496)首次专门研究多巴胺激动剂对PD相关疼痛的影响,并将其作为主要结局。晚期PD患者(即正在接受左旋多巴治疗)且至少患有中度PD相关慢性疼痛(≥3个月,11点李克特疼痛量表评分≥4分)被随机分为罗替戈汀组(最佳/最大剂量≤16 mg/24小时)或安慰剂组,并维持治疗12周。主要疗效变量是从基线到维持期末疼痛严重程度(李克特疼痛量表)的变化。次要变量包括有反应者的百分比(李克特疼痛量表降低≥2分)、国王帕金森疼痛量表(KPPS)各领域以及帕金森病问卷(PDQ-8)。统计分析为探索性分析。在68例随机分组的患者中,60例(罗替戈汀组30例;安慰剂组30例)可进行疗效评估。观察到疼痛有数值上的改善,倾向于罗替戈汀组(李克特疼痛量表:最小二乘均值[95%CI]治疗差异,-0.76[-1.87至0.34];P = 0.172),有反应者的比例为罗替戈汀组18/30(60%),安慰剂组14/30(47%)。与安慰剂相比,罗替戈汀组在KPPS领域“波动相关疼痛”方面观察到约2倍的数值改善。与安慰剂相比,罗替戈汀组改善了PDQ-8(-8.01[-15.56至-0.46];P = 0.038)。这些结果表明罗替戈汀可能改善PD相关疼痛;需要进行大规模的验证性研究。