4.3 Review

Effect of Selective Serotonin Reuptake Inhibitors in Alzheimer's Disease with Comorbid Depression A Meta-Analysis of Depression and Cognitive Outcomes

Journal

DRUGS & AGING
Volume 29, Issue 10, Pages 793-806

Publisher

ADIS INT LTD
DOI: 10.1007/s40266-012-0012-5

Keywords

-

Funding

  1. Canadian Institutes of Health Research (CIHR) (Frederick Banting and Charles Best Canada Graduate Scholarships Doctoral Awards)
  2. Cullen Family, St. Paul's Hospital Foundation
  3. British Columbia (BC) Ministry of Health Services
  4. Baxter
  5. Bristol-Myers-Squibb
  6. Elan
  7. Janssen
  8. Pfizer
  9. Hoffman-La Roche
  10. Genentech
  11. Clinical Genetics Investigatorship award from the CIHR
  12. Genentech at the UBCH-CARD
  13. ADTI
  14. BC Ministry of Health Services through the ADTI
  15. Ralph Fisher Professorship in Alzheimer's (Alzheimer Society of British Columbia)

Ask authors/readers for more resources

Background Comorbid depression is a leading neuropsychiatric complication in the Alzheimer's disease (AD) syndrome. In 2011, diagnostic criteria for AD were revised to include neuropsychiatric symptoms. It has been proposed that adding an antidepressant to existing treatment for AD could provide relief for not only depressive but also cognitive symptoms. Objective The aim was to quantitatively review published studies to examine the efficacy of selective serotonin reuptake inhibitor (SSRI)/serotonin-noradrenaline (norepinephrine) reuptake inhibitor (SNRI) therapy for alleviation of comorbid, diagnosed depression as well as cognitive decline in AD. Methods A search of electronic databases was performed. Studies were retained for analysis if SSRI/SNRI antidepressant therapy was compared with placebo among AD patients with comorbid depression. Effect-size (ES) estimates (Hedges' g) were calculated using Comprehensive Meta-Analysis software. Results From 598 examined studies, 12 SSRI studies met the inclusion criteria, and from these, only six met all criteria, among which five reported sufficient and consistent data to be included in the meta-analysis. Within a random effect model, ES estimates of the first and second nested global analyses were non-significant, non-heterogeneous and small to null at the endpoint for depression, favouring SSRIs, -0.06 and -0.10, respectively (p > 0.05). The ES for global cognition as measured by the Mini-Mental State Examination was negligible (ES = 0.001). Conclusions Current evidence does not support the efficacy of SSRI treatment for symptoms of comorbid depression in AD. However, studies differed in terms of criteria for diagnosis of depression, the compound tested and outcome measures for depression. These factors could account for the lack of a clear benefit for depression.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available