@article{ac3e572113994dd991808b7815e34ae5,
title = "Is sertraline treatment or depression remission in depressed alzheimer patients associated with improved caregiver well being? depression in alzheimer's disease study 2",
abstract = "Objective: We wanted to assess if sertraline treatment (versus placebo) or remission of depression at 12 weeks (versus nonremission) in Alzheimer patients is associated with improved caregiver well being. Methods: We conducted a randomized, double-blind, placebo-controlled clinical trial of the efficacy and safety of sertraline for the treatment of depression in individuals with Alzheimer disease in five clinical research sites across the United States. Participants were caregivers of patients enrolled in the Depression in Alzheimer's Disease Study 2 (N = 131). All caregivers received standardized psychosocial support throughout the study. Caregiver outcome measures included depression (Beck Depression Inventory), distress (Neuropsychiatric Inventory), burden (Zarit Burden Interview), and quality of life (Medical Outcomes Study Short Form Health Survey). Results: Fifty-nine percent of caregivers were spouses, 63.4% were women, and 64.1% were white. Caregivers of patients in both treatment groups had significant reductions in distress scores over the 24-week study period, but there was not a greater benefit for caregivers of patients taking sertraline. However, caregivers of patients whose depression was in remission at week 12 had greater declines in distress scores over the 24 weeks than caregivers of patients whose depression did not remit by week 12. Conclusion: Patient treatment with sertraline was not associated with significantly greater reductions in caregiver distress than placebo treatment. Distress but not level of depression or burden lessened for all caregivers regardless of remission status and even more so for those who cared for patients whose depression remitted. Results imply an interrelationship between caregiver distress and patient psychiatric outcomes. (Am J Geriatr Psychiatry 2014; 22:14-24).",
keywords = "Alzheimer disease, Caregivers, DIADS-2, Depression, Sertraline",
author = "{Flynn Longmire}, {Crystal V.} and Drye, {Lea A} and Frangakis, {Constantine E.} and Martin, {Barbara K.} and Meinert, {Curtis L.} and Mintzer, {Jacobo E.} and Munro, {Cynthia A.} and Porsteinsson, {Anton P.} and Rabins, {Peter V.} and Rosenberg, {Paul B.} and Schneider, {Lon S.} and Daniel Weintraub and Lyketsos, {Constantine G.}",
note = "Funding Information: The following disclosures refer to the period between July 1, 2002 and October 31, 2008 and include any anticipated conflicts through December 31, 2009, according to the DIADS-2 Conflict of Interest Policy (available upon request from the study Principle Investigator). Dr. Martin is involved in another trial for which Pfizer donated a different drug. Dr. Rosenberg has received research funds from Pfizer and Merck in amounts greater than $10,000. Dr. Mintzer has received research support from Abbot to study donepezil and divalproex sodium, from AstraZeneca to study quetiapine, from BMS to study aripiprazole, from Eli Lilly to study olanzapine, from Forest to study both citalopram and memantine, from Janssen to study galantamine and risperidone, and from Pfizer to study donepezil and memantine. Dr. Mintzer also has been a consultant, paid directly or indirectly, for AstraZeneca, BMS, Eli Lilly, Janssen, Pfizer, Forest, and Aventis. He also has been an unpaid consultant for Targacept and has participated in Speaker's Bureaus for Janssen, Forest, and Pfizer. Dr. 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. Dr. 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. Dr. 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. Dr. Rabins has participated on Speaker's Bureaus for Wyeth, Eli Lilly, and Pfizer. Dr. Meinert is involved in another trial for which Pfizer donated a different drug and also owns shares of GSK stock. Dr. Lyketsos was involved in another trial for which Pfizer donated a different drug and 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. All other authors report no conflict of interest. Funding Information: Grant funding was provided by National Institute of Child Health and Human Development and the Office of Research on Women's Health ( K12HD055885 ) and National Institute of Mental Health ( 1U01MH066136, 1U01MH068014, 1U01MH066174, 1U01MH066175, 1U01MH066176, 1U01MH066177 ). National Institute of Mental Health scientific collaborators participated on the trial's Steering Committee. Sertraline and matching placebo were provided by Pfizer, Inc. Pfizer did not participate in the design or conduct of the trial. Manisha Hong, Pharm.D., at Johns Hopkins Hospital Investigational Drug Service packaged and shipped the drugs. ",
year = "2014",
month = jan,
doi = "10.1016/j.jagp.2013.02.014",
language = "English (US)",
volume = "22",
pages = "14--24",
journal = "American Journal of Geriatric Psychiatry",
issn = "1064-7481",
publisher = "Lippincott Williams and Wilkins",
number = "1",
}