Cerebrolysin in Vascular Dementia: Improvement of Clinical Outcome in a Randomized, Double-Blind, Placebo-Controlled Multicenter Trial

被引:45
作者
Guekht, Alla B. [2 ]
Moessler, Herbert
Novak, Philipp H. [1 ]
Gusev, Evgenyi I. [2 ]
机构
[1] Ebewe Neuro Pharma GmbH, Dept Res & Dev, A-4866 Unterach, Austria
[2] Russian State Med Univ, Dept Neurol & Neurosurg, Moscow 117437, Russia
关键词
Vascular dementia; neurotrophic factors; Cerebrolysin; RCT; ALZHEIMERS-DISEASE; COGNITION;
D O I
10.1016/j.jstrokecerebrovasdis.2010.01.012
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
No drug to treat vascular dementia (VaD) has yet been approved by the American or European authorities, leaving a large population of patients without effective therapy. Cerebrolysin has a long record of safety and might be efficacious in this condition. We conducted a large, multicenter, double-blind, placebo-controlled study in 242 patients meeting the criteria for VaD. The primary endpoint was the combined outcome of cognition (based on Alzheimer's Disease Assessment Scale Cognitive Subpart, Extended Version [ADAS-cog+] score) and overall clinical functioning (based on Clinician's Interview-Based Impression of Change plus Caregiver Input [CIBIC +] score) assessed after 24 weeks of treatment. Intravenous Cerebrolysin 20 mL was administered once daily over the course of 2 treatment cycles as add-on therapy to basic treatment with acetylsalicylic acid. The addition of Cerebrolysin was associated with significant improvement in both primary parameters. At week 24, ADAS-cog+ score improved by 10.6 points in the Cerebrolysin group, compared with 4.4 points in the placebo group (least squares mean difference, -6.17; P <.0001 vs placebo). CIBIC+ showed a mean improvement of 2.84 in the treatment arm and 3.68 in the placebo arm, a treatment difference of 0.84 (P <.0001 vs placebo). These findings were confirmed by responder analyses demonstrating higher rates in the Cerebrolysin group (ADAS-cog+ improvement of >= 4points from baseline, 82.1% vs 52.2%; CIBIC+ score of <4 at week 24, 75.3% vs 37.4%; combined response in ADAS-cog+ and CIBIC+, 67.5% vs 27.0%). For Cerebrolysin, the odds ratio for achieving a favorable CIBIC+ response was 5.08 (P <.05), and that for achieving a favorable combined response was 5.63 (P <.05). Our data indicate that the addition of Cerebrolysin significantly improved clinical outcome, and that the benefits persisted for at least 24 weeks. Cerebrolysin was safe and well tolerated.
引用
收藏
页码:310 / 318
页数:9
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