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Cognitive effects of atypical antipsychotic medications in patients with Alzheimer's disease: outcomes from CATIE-AD.

AbstractOBJECTIVE:
The impact of the atypical antipsychotics olanzapine, quetiapine, and risperidone on cognition in patients with Alzheimer's disease is unclear. The authors assessed the effects of time and treatment on neuropsychological functioning during the Clinical Antipsychotic Trials of Intervention Effectiveness-Alzheimer's Disease study (CATIE-AD).
METHOD:
CATIE-AD included 421 outpatients with Alzheimer's disease and psychosis or agitated/aggressive behavior who were randomly assigned to receive masked, flexible-dose olanzapine, quetiapine, risperidone, or placebo. Based on their clinicians' judgment, patients could discontinue the originally assigned medication and receive another randomly assigned medication. Patients were followed for 36 weeks, and cognitive assessments were obtained at baseline and at 12, 24, and 36 weeks. Outcomes were compared for 357 patients for whom data were available for at least one cognitive measure at baseline and one follow-up assessment that took place after they had been on their prescribed medication or placebo for at least 2 weeks.
RESULTS:
Overall, patients showed steady, significant declines over time in most cognitive areas, including in scores on the Mini-Mental State Examination (MMSE; -2.4 points over 36 weeks) and the cognitive subscale of the Alzheimer's Disease Assessment Scale (-4.4 points). Cognitive function declined more in patients receiving antipsychotics than in those given placebo on multiple cognitive measures, including the MMSE, the cognitive subscale of the Brief Psychiatric Rating Scale, and a cognitive summary score summarizing change on 18 cognitive tests.
CONCLUSIONS:
In CATIE-AD, atypical antipsychotics were associated with worsening cognitive function at a magnitude consistent with 1 year's deterioration compared with placebo. Further cognitive impairment is an additional risk of treatment with atypical antipsychotics that should be considered when treating patients with Alzheimer's disease.
AuthorsCheryl L P Vigen, Wendy J Mack, Richard S E Keefe, Mary Sano, David L Sultzer, T Scott Stroup, Karen S Dagerman, John K Hsiao, Barry D Lebowitz, Constantine G Lyketsos, Pierre N Tariot, Ling Zheng, Lon S Schneider
JournalThe American journal of psychiatry (Am J Psychiatry) Vol. 168 Issue 8 Pg. 831-9 (Aug 2011) ISSN: 1535-7228 [Electronic] United States
PMID21572163 (Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Antipsychotic Agents
  • Dibenzothiazepines
  • Benzodiazepines
  • Quetiapine Fumarate
  • Risperidone
  • Olanzapine
Topics
  • Activities of Daily Living (classification, psychology)
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease (diagnosis, drug therapy, psychology)
  • Antipsychotic Agents (adverse effects, therapeutic use)
  • Benzodiazepines (adverse effects, therapeutic use)
  • Cognition Disorders (chemically induced, diagnosis, drug therapy, psychology)
  • Dibenzothiazepines (adverse effects, therapeutic use)
  • Disease Progression
  • Double-Blind Method
  • Drug Substitution
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Mental Status Schedule (statistics & numerical data)
  • Neuropsychological Tests (statistics & numerical data)
  • Olanzapine
  • Patient Dropouts (statistics & numerical data)
  • Quetiapine Fumarate
  • Risperidone (adverse effects, therapeutic use)

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