Quetiapine adjunct to selective serotonin reuptake inhibitors or venlafaxine in patients with major depression, comorbid anxiety, and residual depressive symptoms: a randomized, placebo-controlled pilot study
Open accessAbstract
This double-blind, placebo-controlled study examined the efficacy and tolerability of quetiapine in combination with selective serotonin reuptake inhibitors (SSRIs)/venlafaxine in 58 patients with major depressive disorder, comorbid anxiety symptoms (HAM-A-14 score > or =14), and residual depressive symptoms (HAM-D-17 score > or =18, CGI-S score > or =4). Patients had received an SSRI/venlafaxine (at a predefined therapeutic dose) for > or =6 weeks. Overall, 62% (18/29) of quetiapine- and 55% (16/29) of placebo-treated patients completed the study. The mean change in HAM-D and HAM-A total scores from baseline to Week 8 (primary endpoint) was significantly greater with quetiapine (mean dose 182 mg/day) than placebo: -11.2 vs. -5.5 (P=.008) and -12.5 vs. -5.9 (P=.002), respectively. The onset of quetiapine efficacy (HAM-D/HAM-A/CGI-I) was rapid (by Week 1) and continued through to Week 8. Significant differences (P<.05) from baseline to Week 8 were observed between groups in 7/17 HAM-D (including feelings of guilt, suicide) and 6/14 HAM-A items (including tension, cardiovascular symptoms). Response (> or =50% decrease in total score) was higher for quetiapine than placebo: HAM-D, 48% vs. 28% (not significant, NS); HAM-A, 62% vs. 28% (P=.02). Remission (total score < or =7) was higher for quetiapine than placebo: HAM-D, 31% vs. 17% (NS); HAM-A, 41% vs. 17% (NS). CGI-S, CGI-I, and the Global Assessment Scale showed that quetiapine was significantly more effective than placebo. For quetiapine, adverse events (AEs) were similar to those previously observed; sedation/somnolence/lethargy was the most commonly reported. Here quetiapine was shown to be effective as augmentation of SSRI/venlafaxine therapy in patients with major depression, comorbid anxiety, and residual depressive symptoms, with no unexpected tolerability issues. Further studies are warranted.
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- Authors
- McIntyre, A., Gendron, A., & McIntyre, A.
- Affiliations
- Penticton Regional Hospital (CA)
- AstraZeneca (Canada) (CA)
- Corresponding author
- McIntyre, Alexander
- ORCID
- Gendron, Alain
- Venue
- Depression and Anxiety
- Publisher
- Wiley
- Published
- 2007
- Volume
- 24
- Issue
- 7
- Pages
- 487-494
- ISSN
- 1091-4269 (ISSN-L)
- 1520-6394
- OpenAlex
- W2065791141
- Cited by
- 145
- References
- 35
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 4 · 2023: 8 · 2022: 5 · 2021: 5 · 2020: 4 · 2019: 4 · 2018: 1 · 2017: 5 · 2016: 4 · 2015: 13 · 2014: 7 · 2013: 18 · 2012: 3
- FWCI
- 5.64
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Depression and Anxiety (publishedVersion)
- PubMed (publishedVersion)
- Funders
- AstraZeneca
- National Institute of Mental Health
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Keywords
- quetiapine, major depressive disorder, anxiety comorbidity, residual depressive symptoms, selective serotonin reuptake inhibitors, venlafaxine, adjunctive therapy, atypical antipsychotics, antidepressant efficacy, tolerability, adverse events, sedation, remission, Hamilton Depression Rating Scale, Hamilton Anxiety Rating Scale, CGI-S, CGI-I, Global Assessment Scale
- MeSH terms
- Quetiapine Fumarate, Venlafaxine Hydrochloride, Adult, Anxiety Disorders, Cyclohexanols, Major Depressive Disorder, Dibenzothiazepines, Double-Blind Method, Drug Therapy, Combination, Female, Humans, Male, Middle Aged, Personality Inventory, Antipsychotic Agents, Comorbidity, Selective Serotonin Reuptake Inhibitors, Antidepressive Agents, Second-Generation
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