Cognitive outcomes after sertaline treatment in patients with depression of Alzheimer disease
- PMID: 23032478
- PMCID: PMC3508666
- DOI: 10.1097/JGP.0b013e31826ce4c5
Cognitive outcomes after sertaline treatment in patients with depression of Alzheimer disease
Abstract
Objectives: Although many depressed patients with Alzheimer disease (AD) are treated with antidepressants, the effect of such treatment on cognitive performance in these patients is not known. The authors report cognitive outcomes in patients with depression of AD (dAD) after a 24-week trial of sertraline or placebo.
Design: Placebo-controlled, randomized, double-blind trial.
Setting: Outpatient memory clinics at five academic medical centers in the United States.
Participants: A total of 131 patients with dAD (60 men) and Mini-Mental State Examination scores of 10-26.
Intervention: Sertraline (n = 67), target dose of 100 mg daily or matching placebo (n = 64). Caregivers received standardized psychosocial intervention throughout the trial.
Measurements: Mini-Mental State Examination, cognitive subscale of the Alzheimer's Disease Assessment Scale, letter fluency, backward digit span, Symbol Digit Modalities Test, and Finger Tapping Test, administered at baseline, and 8, 16, and 24 weeks following baseline.
Results: A series of linear models indicated no effect of treatment or of depression remission on cognitive test performance at 24 weeks. Regardless of treatment condition, very little change in cognitive test performance was noted in general.
Conclusions: Treatment with sertraline in patients with dAD is not associated with greater improvement in cognition at week 24 than treatment with placebo.
Conflict of interest statement
These disclosures include any anticipated conflicts through 9/31/11, according to the DIADS-2 Conflict of Interest Policy (available upon request from the study PI).
Barbara Martin is involved in another trial for which Pfizer donated a different drug.
Paul Rosenberg has received research funds from Pfizer and Merck in amounts greater than $10,000.
Jacobo Mintzer is a current grant recipient for Wyeth, Lilly and Pfizer.
Daniel Weintraub has received research support from Boehringer Ingelheim; Dr. Weintraub also has been a paid consultant for Acadia Pharmaceuticals, Novartis Pharmaceuticals, Boehringer Ingelheim, Osmotica Pharmaceutical, BrainCells Inc., EMD Serono, and Sanofi Aventis, and has participated on a Speaker’s Bureau for Pfizer.
Anton Porsteinsson is involved in research sponsored by Pfizer to study donepezil and PF04494700, Eli Lilly to study atomoxetine, a gamma-secretase inhibitor and a beta amyloid antibody, Wyeth to study a beta amyloid antibody, GSK to study a PPAR inhibitor and Forest to study memantine and neramexane; Dr. Porsteinsson has been a paid consultant and participated on a Speaker's Bureau for Pfizer and Forest.
Lon S. Schneider is involved in research sponsored by Pfizer, the manufacturer of sertraline and other drugs used to treat mood disorders; Dr. Schneider has been a paid consultant for Abbott, AstraZeneca, Eli Lilly, Forest, GlaxoSmithKline, Johnson and Johnson, Lundbeck, Merck, and Wyeth, manufacturers of antidepressants or drugs used to treat mood disorders.
Constantine Frangakis has no conflict of interests.
Lea Drye has no conflict of interests.
Peter Rabins has participated on Speaker's Bureaus for Wyeth, Eli Lilly, and Pfizer more than two years previous. He has provided legal testimony for Janssen Pharmaceutica.
Cynthia Munro has no conflict of interests.
Curtis Meinert is involved in another trial for which Pfizer donated a different drug; Dr. Meinert owns shares of GSK stock.
Constantine Lyketsos was involved in another trial for which Pfizer donated a different drug; he also was involved in research sponsored by Forest to study escitalopram and citalopram and Pfizer to study sertraline and donepezil; Dr. Lyketsos served as a consultant for Organon, Eisai, GSK, Lilly, Wyeth, and Pfizer.
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