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首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Randomized, placebo-controlled, clinical trial of donepezil in vascular dementia: differential effects by hippocampal size.
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Randomized, placebo-controlled, clinical trial of donepezil in vascular dementia: differential effects by hippocampal size.

机译:多奈哌齐治疗血管性痴呆的随机,安慰剂对照临床试验:海马体大小的不同影响。

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摘要

BACKGROUND AND PURPOSE: We sought to assess the efficacy and safety of donepezil in patients with vascular dementia (VaD) fulfilling National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche et l'Enseignement en Neurosciences criteria. METHODS: This international, multicenter, 24-week trial was conducted from March 2003 to August 2005. Patients (N=974; mean age, 73.0 years) with probable or possible VaD were randomized 2:1 to receive donepezil 5 mg/d or placebo. Coprimary outcome measures were scores on the Vascular-Alzheimer Disease Assessment Scale-Cognitive Subscale and Clinician's Interview-Based Impression of Change, plus carer interview. Analyses were performed for the intent-to-treat population with the last-observation-carried-forward method. RESULTS: Compared with placebo, donepezil-treated patients showed significant improvement from baseline to end point on the Vascular-Alzheimer Disease Assessment Scale-Cognitive Subscale (least-squares mean difference, -1.156; 95% CI, -1.98 to -0.33; P<0.01) but not on the Clinician's Interview-Based Impression of Change, plus carer interview. Patients with hippocampal atrophy who were treated with donepezil demonstrated stable cognition versus a decline in the placebo-treated group; in those without atrophy, cognition improved with donepezil versus relative stability with placebo. Results on secondary efficacy measures were inconsistent. The incidence of adverse events was similar across groups. Eleven deaths occurred in the donepezil group (1.7%), similar to rates previously reported for donepezil trials in VaD, whereas no deaths occurred in the placebo group. CONCLUSIONS: Patients treated with donepezil 5 mg/d demonstrated significant improvement in cognitive, but not global, function. Donepezil was relatively well tolerated; adverse events were consistent with current labeling. Mortality in the placebo group was unexpectedly low. The differential treatment response of VaD patients by hippocampal size suggests that hippocampal imaging warrants further investigation for understanding VaD.
机译:背景与目的:我们试图评估多奈哌齐在血管性痴呆(VaD)患者中的疗效和安全性,符合美国国家神经疾病学会和中风协会神经科学研究标准的要求。方法:这项国际性的,多中心的,为期24周的试验于2003年3月至2005年8月进行。将可能或可能存在VaD的患者(N = 974;平均年龄,73.0岁)随机分2:1接受多奈哌齐5 mg / d或安慰剂。共同主要结局指标是血管性阿尔茨海默病评估量表,认知亚量表和临床医生基于面试的变化印象评分,以及护理人员访谈。采用最后观察携带前移法对意向性治疗人群进行了分析。结果:与安慰剂相比,多奈哌齐治疗的患者在血管阿尔茨海默病疾病评估量表-认知子量表上从基线到终点均有显着改善(最小二乘法均值为-1.156; 95%CI为-1.98至-0.33; P <0.01),但不是基于临床医生基于面试的变化印象,以及护理人员面试。用多奈哌齐治疗的海马萎缩患者表现出稳定的认知,而安慰​​剂治疗组却有所下降。在没有萎缩的患者中,多奈哌齐的认知度相对于安慰剂相对稳定。次要疗效测量结果不一致。各组之间不良事件的发生率相似。多奈哌齐组有11例死亡(1.7%),与先前在VaD中多奈哌齐试验报告的发生率相似,而安慰剂组没有死亡。结论:多奈哌齐5 mg / d治疗的患者认知功能显着改善,但总体功能未见改善。多奈哌齐的耐受性相对较好。不良事件与当前标签一致。安慰剂组的死亡率出乎意料地低。根据海马体大小对VaD患者的不同治疗反应表明,海马成像值得进一步研究以了解VaD。

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