Sertraline for the Treatment of Depression in Alzheimer Disease: Genetic Influences

被引:11
|
作者
Peters, Matthew E. [1 ]
Vaidya, Vijay [2 ]
Drye, Lea T. [2 ]
Rosenberg, Paul B. [1 ]
Martin, Barbara K. [2 ]
Porsteinsson, Anton P. [3 ]
Frangakis, Constantine E. [2 ]
Mintzer, Jacobo [4 ,5 ]
Weintraub, Daniel [6 ]
Schneider, Lon S. [7 ]
Rabins, Peter V. [1 ]
Munro, Cynthia A. [1 ]
Meinert, Curtis L. [2 ]
Lyketsos, Constantine G. [1 ]
Dimitri, Avramopoulos [1 ]
机构
[1] Johns Hopkins Univ, Baltimore, MD 21224 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[3] Univ Rochester, Rochester, NY USA
[4] Med Univ S Carolina, Charleston, SC 29425 USA
[5] Ralph H Johnson VA Med Ctr, Charleston, SC USA
[6] Univ Penn, Philadelphia, PA 19104 USA
[7] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
Alzheimer disease; sertraline; depression; randomized trial; dementia; antidepressant; DOUBLE-BLIND; NEUROPSYCHIATRIC SYMPTOMS; CLINICAL-TRIAL; POLYMORPHISM; DEMENTIA; PREVALENCE; PSYCHOSIS; EFFICACY; CRITERIA;
D O I
10.1177/0891988711422527
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objective. To assess the potential for genetic influences on sertraline treatment efficacy for depression of Alzheimer disease (dAD). Four functional genetic variants were studied: 2 serotonin receptors (HTR2A-T102C and HTR2C-Cys23Ser), the serotonin transporter (5HTT-LPR), and brain-derived neurotrophic factor (BDNF-Val66Met). Treatment response by genotype was measured by (1) the modified Alzheimer's Disease Cooperative Study Clinical Global Impression of Change, (2) the Cornell scale for Depression in Dementia, and (3) remission of depression. Methods. We utilized data from the Depression in Alzheimer's Disease Study 2 (DIADS-2), a 24-week, randomized, multicenter trial showing no significant treatment effect of sertraline on dAD. Proportional odds logistic regression and mixed effects models were used to examine the above mentioned outcome measures. Results. No significant interactions were seen between any of the genetic polymorphisms and the selected outcomes above at 12 or 24 weeks. Discussion. Treatment outcomes in the DIADS-2 trial were not significantly influenced by genetic variation at the loci that were assessed. Future studies should continue to examine the interaction of depression-related genetic variants with antidepressant treatment in Alzheimer disease patients with depression.
引用
收藏
页码:222 / 228
页数:7
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