Randomized, placebo-controlled trial of the effects of donepezil on neuronal markers and hippocampal volumes in Alzheimer's disease

被引:197
作者
Krishnan, KRR [1 ]
Charles, HC
Doraiswamy, PM
Mintzer, J
Weisler, R
Yu, X
Perdomo, C
Ieni, JR
Rogers, S
机构
[1] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27710 USA
[2] Eisai Inc, Teaneck, NJ USA
[3] Med Univ S Carolina, Dept Psychiat, Charleston, SC 29425 USA
[4] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Radiol, Durham, NC 27710 USA
关键词
D O I
10.1176/appi.ajp.160.11.2003
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The authors examined the effect of the acetylcholinesterase inhibitor donepezil on magnetic resonance markers of neurodegeneration in Alzheimer's disease. Method: In this randomized, double-blind, placebo-controlled pilot study, 67 patients with mild to moderate Alzheimer's disease received 24 weeks of treatment with donepezil (5 mg/day for the first 28 days and 10 mg/day thereafter) or placebo. Patients were reevaluated at 6-week intervals to measure change from baseline in several outcome measures, including right, left, and total hippocampal volumes, measured with magnetic resonance imaging; brain concentrations of N-acetylaspartate, measured with proton magnetic resonance spectroscopy; and cognition, assessed with the Alzheimer's Disease Assessment Scale cognitive subscale. Results: At some interim assessments, mean normalized measures of N-acetylaspartate concentration tended to be higher in the donepezil-treated patients than in the patients who received placebo, but these differences were not significant at endpoint. At endpoint, the donepezil-treated patients had significantly smaller mean decreases in total and right hippocampal volumes and a smaller, nearly significant mean decrease in left hippocampal volume, compared with the placebo-treated patients. Mean Alzheimer's Disease Assessment Scale cognitive subscale scores were improved after treatment with donepezil, relative to placebo, at weeks 6, 12, 18, and 24. Conclusions: These preliminary results suggest that donepezil may have a potentially protective effect in Alzheimer's disease. Larger, longer-term confirmatory studies of the medication's effects are warranted.
引用
收藏
页码:2003 / 2011
页数:9
相关论文
共 42 条
[1]   Longitudinal decline of the neuronal marker N-acetyl aspartate in Alzheimer's disease [J].
Adalsteinsson, E ;
Sullivan, EV ;
Kleinhans, N ;
Spielman, DM ;
Pfefferbaum, A .
LANCET, 2000, 355 (9216) :1696-1697
[2]   Advances in intravenous thrombolytic therapy for treatment of acute stroke [J].
Albers, GW .
NEUROLOGY, 2001, 57 (05) :S77-S81
[3]   Functions of N-acetyl-L-aspartate and N-acetyl-L-aspartylglutamate in the vertebrate brain:: Role in glial cell-specific signaling [J].
Baslow, MH .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (02) :453-459
[4]   Reproducibility of high spatial resolution proton magnetic resonance spectroscopic imaging in the human brains [J].
Charles, HC ;
Lazeyras, F ;
Tupler, LA ;
Krishnan, KRR .
MAGNETIC RESONANCE IN MEDICINE, 1996, 35 (04) :606-610
[5]   Alzheimer disease [J].
Cummings, JL ;
Cole, G .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (18) :2335-2338
[6]   Early N-acetylaspartate depletion is a marker of neuronal dysfunction in rats and primates chronically treated with the mitochondrial toxin 3-nitropropionic acid [J].
Dautry, W ;
Vaufrey, F ;
Brouillet, E ;
Bizat, N ;
Henry, PG ;
Condé, F ;
Bloch, G ;
Hantraye, P .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (05) :789-799
[7]   N-Acetylaspartate, a marker of both cellular dysfunction and neuronal loss:: its relevance to studies of acute brain injury [J].
Demougeot, C ;
Garnier, P ;
Mossiat, C ;
Bertrand, N ;
Giroud, M ;
Beley, A ;
Marie, C .
JOURNAL OF NEUROCHEMISTRY, 2001, 77 (02) :408-415
[8]  
DESTEFANO N, 1995, MAGN RESON MED, V34, P721
[9]  
DORAISWAMY, 1995, LANCET, V345, P1250
[10]   Brain magnetic resonance spectroscopy - Role in assessing outcomes in Alzheimer's disease [J].
Doraiswamy, PM ;
Chen, JG ;
Charles, HC .
CNS DRUGS, 2000, 14 (06) :457-472