Brennan Laura, Pantelyat Alexander, Duda John E, Morley James F, Weintraub Daniel, Wilkinson Jayne R, Moberg Paul J
Parkinson's Disease Research, Education and Clinical Center (PADRECC) Philadelphia Veteran's Affairs Hospital Philadelphia Pennsylvania USA.
Department of Psychiatry University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA.
Mov Disord Clin Pract. 2015 Dec 7;3(2):161-167. doi: 10.1002/mdc3.12264. eCollection 2016 Mar-Apr.
The aim of this work was to utilize meta-analysis in examining the effects of memantine on neuropsychological functioning in patients with Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB).
Included studies fulfilled these criteria: included objective cognitive measures, a comparison group of participants not taking memantine, and provided sufficient data for calculation of effect size. We examined effect sizes across global cognition and five specific neuropsychological domains. Moderator variables examined included neuropsychological domain, diagnostic cohort (PDD, DLB, or mixed PDD-DLB cohort), study design (open label or placebo-controlled), and trial length.
Six publications met inclusion criteria totaling 57 effects. Homogeneity analysis across cognitive domains revealed a small overall effect size ( = 0.25) that was significantly heterogeneous ( < 0.001). Specific neuropsychological domains did not moderate effect size, though. Moderator analysis studies using a mix of DLB and PDD subjects showed larger effects than those that included DLB or PDD patients only. Additionally, open-label trials had significantly ( < 0.001) larger effect sizes ( = 1.32) than placebo-controlled trials ( = 0.12).
The present study indicates that effect-size heterogeneity across studies of memantine in DLB and PDD patients is moderated by diagnostic makeup of the cohort and study design. The small overall effect size noted in placebo-controlled trials versus open-label trials indicates that memantine has minimal effects on cognition in PDD and DLB and is unlikely to demonstrate clinically significant improvements in cognition.
本研究旨在利用荟萃分析来检验美金刚对帕金森病痴呆(PDD)和路易体痴呆(DLB)患者神经心理功能的影响。
纳入的研究需满足以下标准:包括客观认知测量、未服用美金刚的参与者对照组,并提供足够的数据用于计算效应量。我们研究了整体认知和五个特定神经心理领域的效应量。所考察的调节变量包括神经心理领域、诊断队列(PDD、DLB或PDD - DLB混合队列)、研究设计(开放标签或安慰剂对照)以及试验时长。
六项出版物符合纳入标准,共计57个效应量。跨认知领域的同质性分析显示,总体效应量较小( = 0.25),且存在显著异质性( < 0.001)。不过,特定神经心理领域并未调节效应量。使用DLB和PDD受试者混合样本的调节分析研究显示,其效应大于仅纳入DLB或PDD患者的研究。此外,开放标签试验的效应量( = 1.32)显著( < 0.001)大于安慰剂对照试验( = 0.12)。
本研究表明,在DLB和PDD患者中,美金刚研究的效应量异质性受队列的诊断构成和研究设计的调节。安慰剂对照试验与开放标签试验中观察到的总体效应量较小,表明美金刚对PDD和DLB患者的认知影响极小,不太可能在认知方面显示出具有临床意义的改善。