Department of Neurological Sciences, University of Liverpool, The Walton Centre for Neurology and Neurosurgery, Lower Lane, Liverpool, L9 7LJ, UK.
J Neurol. 2010 Mar;257(3):452-6. doi: 10.1007/s00415-009-5351-8. Epub 2009 Oct 20.
Fatigue is common in Parkinson's disease (PD), occurring in up to 42% of patients (2). There is no recognized treatment. This is a study of modafinil for Parkinson's disease related fatigue. Ethical approval was given. Patients with idiopathic PD were recruited from a Movement Disorders clinic. Those with depression, dementia, and other causes for fatigue were excluded. Patients were assessed using the Fatigue Severity Scale (FSS), Hospital Anxiety and Depression Scale (HADS), self-rating of improvement, Epworth Sleepiness Scale (ESS), and UPDRS. Modafinil was titrated up over 4 weeks to maximum of 400 mg/day. There followed a 5 week maintenance phase before reassessment. Thirteen patients participated. No significant change was seen in any safety measure. The FSS did not change significantly, however those on modafinil rated an improvement in their fatigue compared to placebo. The Modafinil group had a statistically significant improvement on ESS (p < 0.05). This is a small study of modafinil in selected PD patients. There is a suggestion of improvement on the global clinical impression scale for fatigue, but no significant change on FSS. A larger study is needed to further evaluate this drug in PD fatigue. This study highlights the problems with recruitment when trialing treatments of non-motor symptoms in PD. A significant improvement in EDS was seen.
疲劳是帕金森病(PD)的常见症状,多达 42%的患者(2)会出现这种症状。目前尚无公认的治疗方法。这是一项关于莫达非尼治疗帕金森病相关疲劳的研究。本研究已获得伦理批准。特发性 PD 患者从运动障碍诊所招募。排除有抑郁、痴呆和其他导致疲劳的原因的患者。使用疲劳严重程度量表(FSS)、医院焦虑和抑郁量表(HADS)、自我改善评分、Epworth 嗜睡量表(ESS)和 UPDRS 对患者进行评估。莫达非尼在 4 周内逐渐增加剂量,最大剂量为 400mg/天。随后进行 5 周的维持阶段,然后重新评估。共有 13 名患者参与。任何安全措施均未发生显著变化。FSS 无显著变化,但与安慰剂相比,使用莫达非尼的患者对疲劳的改善评分更高。莫达非尼组在 ESS 上有统计学意义的改善(p<0.05)。这是一项针对选定 PD 患者的莫达非尼小型研究。疲劳的全球临床印象量表有改善的迹象,但 FSS 没有显著变化。需要更大规模的研究来进一步评估这种药物在 PD 疲劳中的作用。这项研究强调了在 PD 非运动症状治疗中进行试验时招募患者存在的问题。EDs 显著改善。