Presence or absence of at least one ε4 allele and gender are not predictive for the response to donepezil treatment in Alzheimer's disease

被引:65
作者
Rigaud, AS
Traykov, L
Latour, F
Couderc, R
Moulin, F
Forette, F
机构
[1] Univ Paris 05, Hop Broca, CHU Cochin Port Royal, F-75013 Paris, France
[2] INSERM, Unit 324, Paris, France
[3] Hop Trousseau, Dept Biochem, F-75571 Paris, France
来源
PHARMACOGENETICS | 2002年 / 12卷 / 05期
关键词
Alzheimer's disease; dementia; apolipoprotein E; epsilon; 4; allele; donepezil;
D O I
10.1097/00008571-200207000-00009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The objective was to evaluate the effects of the apolipoprotein E (ApoE) genotype and gender on the response to donepezil treatment in Alzheimer's disease. ApoE genotyping was performed on 117 patients with mild to moderate Alzheimer's disease who were included in a 36-week open label trial of donepezil therapy. Of these 117 patients, who constituted the intent-to-treat population (ITT), 80 completed the trial, and constituted the evaluable population. Patients were treated blindly in relation to ApoE genotype. Outcome measures were Alzheimer's disease Assessment Scale-Cognitive Component (ADASCog), the Mini Mental State Examination, Instrumental Activities of Daily Living, and the Caregiver-rated Clinical Global Impression of Change. ITT analysis did not reveal significant differences between the responses Of epsilon4- and epsilon4+ carriers according to the ADAS-Cog (P = 0.28). No differences were found either between the responses of men and women (P= 0.81), and there was no significant interaction between genotype and gender (P = 0.09). Other outcome measures all exhibited similar patterns of change to those seen using the ADAS-Cog. Consequently, these results do not support the hypothesis that the ApoE phenotype and gender are predictors of the response to donepezil in Alzheimer's disease patients.
引用
收藏
页码:415 / 420
页数:6
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