Treatment outcome of tacrine therapy depends on apolipoprotein genotype and gender of the subjects with Alzheimer's disease

Martin R. Farlow, D. K. Lahiri, J. Poirier, J. Davignon, L. Schneider, S. L. Hui

Research output: Contribution to journalArticle

169 Scopus citations

Abstract

We studied the effects of apolipoprotein E (APOE) genotype and gender on clinical response to tacrine in patients with mild to moderate Alzheimer's disease (AD). We analyzed data from a previously reported 30-week, double- blind, placebo-controlled trial of tacrine, in which APOE genotypes were determined from previously collected plasma samples. Patients were assigned to placebo or tacrine with daily dosages of 80, 120, or 160 mg/day. The outcome measures were Alzheimer's Disease Assessment Scale-Cognitive Component, Clinician Interview Based Impression, Mini-Mental State Examination, and the Caregiver-rated Clinical Global Impression of Change. An intent-to-treat (ITT) analysis of patients with available genotypes (n = 528) did not reveal response differences by genotype, although the effect size was twice as large in the ε2-3 as the ε4 group (-2.62 versus -1.25). The association of treatment effect with APOE genotype varied significantly according to gender (p < 0.002 for ITT; p < 0.05 for evaluables). The treatment effect was larger in the ε2-3 compared with ε4 women (ITT, 4.24 points, p = 0.03; evaluable, 7.20 points, p = 0.01). In contrast, treatment effect size was not different between ε2-3 and ε4 of men with AD. APOE genotype and gender may predict response to tacrine in patients with AD.

Original languageEnglish (US)
Pages (from-to)669-677
Number of pages9
JournalNeurology
Volume50
Issue number3
DOIs
StatePublished - Mar 1998

ASJC Scopus subject areas

  • Clinical Neurology

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