Barone P, Santangelo G, Morgante L, Onofrj M, Meco G, Abbruzzese G, Bonuccelli U, Cossu G, Pezzoli G, Stanzione P, Lopiano L, Antonini A, Tinazzi M
University of Salerno, Baronissi, Italy.
Second University of Naples, Caserta, Italy.
Eur J Neurol. 2015 Aug;22(8):1184-91. doi: 10.1111/ene.12724. Epub 2015 May 12.
Depressed mood is a common psychiatric problem associated with Parkinson's disease (PD), and studies have suggested a benefit of rasagiline treatment.
ACCORDO (see the ) was a 12-week, double-blind, placebo-controlled trial to evaluate the effects of rasagiline 1 mg/day on depressive symptoms and cognition in non-demented PD patients with depressive symptoms. The primary efficacy variable was the change from baseline to week 12 in depressive symptoms measured by the Beck Depression Inventory (BDI-IA) total score. Secondary outcomes included change from baseline to week 12 in cognitive function as assessed by a comprehensive neuropsychological battery; Parkinson's disease quality of life questionnaire (PDQ-39) scores; Apathy Scale scores; and Unified Parkinson's Disease Rating Scale (UPDRS) subscores.
One hundred and twenty-three patients were randomized. At week 12 there was no significant difference between groups for the reduction in total BDI-IA score (primary efficacy variable). However, analysis at week 4 did show a significant difference in favour of rasagiline (marginal means difference ± SE: rasagiline -5.46 ± 0.73 vs. placebo -3.22 ± 0.67; P = 0.026). There were no significant differences between groups on any cognitive test. Rasagiline significantly improved UPDRS Parts I (P = 0.03) and II (P = 0.003) scores versus placebo at week 12. Post hoc analyses showed the statistical superiority of rasagiline versus placebo in the UPDRS Part I depression item (P = 0.04) and PDQ-39 mobility (P = 0.007) and cognition domains (P = 0.026).
Treatment with rasagiline did not have significant effects versus placebo on depressive symptoms or cognition in PD patients with moderate depressive symptoms. Although limited by lack of correction for multiple comparisons, post hoc analyses signalled some improvement in patient-rated cognitive and depression outcomes.
情绪低落是帕金森病(PD)常见的精神问题,研究表明雷沙吉兰治疗有益。
ACCORDO(见 )是一项为期12周的双盲、安慰剂对照试验,旨在评估雷沙吉兰1毫克/天对有抑郁症状的非痴呆PD患者抑郁症状和认知的影响。主要疗效变量是用贝克抑郁量表(BDI-IA)总分衡量的从基线到第12周抑郁症状的变化。次要结局包括通过综合神经心理测验评估的从基线到第12周认知功能的变化;帕金森病生活质量问卷(PDQ-39)得分;淡漠量表得分;以及统一帕金森病评定量表(UPDRS)分项得分。
123例患者被随机分组。在第12周时,两组间BDI-IA总分降低(主要疗效变量)无显著差异。然而,第4周的分析确实显示雷沙吉兰组有显著差异(边际均值差异±标准误:雷沙吉兰-5.46±0.73 vs.安慰剂-3.22±0.67;P = 0.026)。在任何认知测试中,两组间均无显著差异。在第12周时,与安慰剂相比,雷沙吉兰显著改善了UPDRS第一部分(P = 0.03)和第二部分(P = 0.003)得分。事后分析显示,在UPDRS第一部分抑郁项目(P = 0.04)、PDQ-39运动(P = 0.007)和认知领域(P = 0.026)中,雷沙吉兰相对于安慰剂具有统计学优势。
对于有中度抑郁症状的PD患者,雷沙吉兰治疗在抑郁症状或认知方面与安慰剂相比无显著效果。尽管因缺乏多重比较校正而有局限性,但事后分析表明患者自评的认知和抑郁结局有一些改善。