Geva Michal, Goldberg Y Paul, Schuring Henk, Tan Andrew M, Long Jeffrey D, Hayden Michael R
Prilenia Therapeutics B.V, Naarden, The Netherlands.
Department of Neurology, Yale University School of Medicine, New Haven, Connecticut, USA.
Mov Disord. 2025 May;40(5):928-937. doi: 10.1002/mds.30164. Epub 2025 Mar 18.
Antidopaminergic medications (ADM) are often used for symptom management of Huntington's disease (HD). Evidence from past research suggests that ADMs are associated with worse clinical outcomes in HD, but their impact on various domains remains underexplored.
We used causal inference analysis to understand the impact of ADM use on measures of clinical progression in HD across multiple domains over 2 years.
We used the Enroll-HD database with a new-user design, which compared a cohort that initiated ADM use after the first visit with an unexposed cohort that remained off ADMs. To control for 27 covariates, we used a doubly robust targeted maximum likelihood estimation and conducted two analyses. First, we analyzed ADM treatment 2 years post-baseline and separately for 12 outcome measures. Second, we examined the association of ADM dose with measures of clinical outcomes.
The ADM-exposed group exhibited faster change in measures of clinical outcome compared with the off-ADM group, which was statistically reliable in cognitive and functional outcome measures, and the composite Unified Huntington's Disease Rating Scale (cUHDRS). Motor domain analyses showed faster change in bradykinesia in the ADM-exposed group versus off-ADM but no difference in chorea or total motor score (TMS). Higher ADM doses also showed greater differences compared to the off-ADM group.
ADM use was associated with more rapid change in clinical measures, particularly in cognitive and functional domains. However, assumptions required to establish causation between ADM use and disease progression may not have been fully met, and further research is warranted. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
抗多巴胺能药物(ADM)常用于亨廷顿病(HD)的症状管理。以往研究证据表明,ADM与HD更差的临床结局相关,但其对各个领域的影响仍未得到充分探索。
我们采用因果推断分析来了解ADM使用对HD患者2年多来多个领域临床进展指标的影响。
我们使用了Enroll-HD数据库,采用新用户设计,将首次就诊后开始使用ADM的队列与未使用ADM的未暴露队列进行比较。为了控制27个协变量,我们使用了双重稳健的靶向最大似然估计,并进行了两项分析。首先,我们分析了基线后2年的ADM治疗情况,并分别针对12项结局指标进行分析。其次,我们研究了ADM剂量与临床结局指标之间的关联。
与未使用ADM的组相比,使用ADM的组在临床结局指标上的变化更快,这在认知和功能结局指标以及综合统一亨廷顿病评定量表(cUHDRS)中具有统计学可靠性。运动领域分析显示,使用ADM的组与未使用ADM的组相比,运动迟缓变化更快,但舞蹈症或总运动评分(TMS)没有差异。与未使用ADM的组相比,更高剂量的ADM也显示出更大的差异。
使用ADM与临床指标的更快变化相关,特别是在认知和功能领域。然而,在确定ADM使用与疾病进展之间的因果关系所需的假设可能尚未完全满足,因此有必要进行进一步研究。© 2025作者。《运动障碍》由Wiley Periodicals LLC代表国际帕金森和运动障碍协会出版。