Mouradian M Maral, Stoessl A Jon, Lang Anthony E
Robert Wood Johnson Medical School Institute for Neurological Therapeutics, and Department of Neurology, Rutgers Health, Piscataway, New Jersey, USA.
Djavad Mowafaghian Centre for Brain Health, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Mov Disord. 2025 Sep;40(9):1778-1790. doi: 10.1002/mds.30259. Epub 2025 Jul 10.
Traditionally, clinical trials of putative disease-modifying therapies in Parkinson's disease have enrolled untreated patients at the earliest clinical stages of their disease. Due to a number of challenges inherent with this approach, there has been a recent move to a different study design, enrolling patients who are already taking "stable" anti-parkinson medication. However, typically, the symptomatic treatment regimen has not been defined uniformly with respect to drugs and dosages utilized or duration of therapy. More importantly, this approach fails to consider or account for the major pharmacodynamic changes induced in the parkinsonian brain by varying dopaminergic therapies (particularly levodopa) and the impact of these on both clinical and neuroimaging outcome measures. In this review, we highlight what is known about the changes induced by dopaminergic therapy and the challenges these will present in the interpretation of outcomes of studies using this trial design. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
传统上,帕金森病潜在疾病修饰疗法的临床试验纳入的是处于疾病最早临床阶段且未接受过治疗的患者。由于这种方法存在一些固有的挑战,最近已转向一种不同的研究设计,即纳入已经在服用“稳定”抗帕金森药物的患者。然而,通常在所用药物和剂量或治疗持续时间方面,对症治疗方案并未得到统一界定。更重要的是,这种方法没有考虑或说明不同多巴胺能疗法(尤其是左旋多巴)在帕金森病大脑中引起的主要药效学变化,以及这些变化对临床和神经影像学结局指标的影响。在本综述中,我们强调了关于多巴胺能疗法引起的变化的已知情况,以及这些变化在解释采用这种试验设计的研究结果时所带来的挑战。© 2025作者。《运动障碍》由威利期刊有限责任公司代表国际帕金森和运动障碍协会出版。