Effects of a flexible galantamine dose in Alzheimer's disease: a randomised, controlled trial

被引:218
作者
Rockwood, K
Mintzer, J
Truyen, L
Wessel, T
Wilkinson, D
机构
[1] QEII Hlth Sci Ctr, Ctr Hlth Care Elderly, Halifax, NS B3H 2E1, Canada
[2] Med Univ S Carolina, Dept Psychiat, Charleston, SC 29425 USA
[3] Janssen Res Fdn, B-2340 Beerse, Belgium
[4] Janssen Res Fdn, Titusville, NJ USA
关键词
Alzheimer's disease; galantamine; nicotinic receptors; acetylcholinesterase inhibition; activities of daily living;
D O I
10.1136/jnnp.71.5.589
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective-To assess the efficacy and safety of galantamine in Alzheimer's disease at 3 months using flexible dose escalation. Methods-A randomised, double blind, placebo controlled trial in 43 centres in the United States, Canada, Great Britain, South Africa, Australia, and New Zealand. Patients with probable Alzheimer's disease (n=386; 171 women) with a score of 11-24 on the mini mental state examination, and a score greater than or equal to 12 on the cognitive subscale of the Alzheimer's disease assessment scale (ADAS-cog) were randomised to placebo, or galantamine escalated over 4 weeks to a maintenance dose of 24 or 32 mg/day. The primary outcome measures were the change in ADAS-cog score and the clinician's interview based impression of change plus caregiver input (CIBIC-plus) score. Activities of daily living (ADL) and behavioural symptoms were secondary outcomes. To compare the effects of highest levels of dosing, an observed cases (OC) analysis was undertaken, with classic intention to treat (ITT) and ITT with last observation carried forward (LOCF) as confirmatory analyses. Results-At 3 months, galantamine (24-32 mg/day) produced a significantly better outcome on cognitive function than placebo (treatment difference=1.9 points on ADAS-cog, p=0.002) and a significantly better global response than placebo, as measured by CIBIC-plus (deterioration in 21% of patients on galantamine v 37% on placebo; p <0.001). Galantamine produced significant benefits on basic and instrumental ADL. Behavioural. symptoms did not change significantly from baseline levels in either group. Adverse events (primarily gastrointestinal) were of Mild to moderate intensity. There were no important differences between the OC, ITT, and ITT/LOCF analyses. Most patients (82%) who were maintained on the higher dose of galantamine completed the study. Conclusions-Patients on galantamine, compared with those on placebo, experienced benefits in cognitive function and instrumental and basic activities of daily living. Flexible dose escalation of galantamine was well tolerated.
引用
收藏
页码:589 / 595
页数:7
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