4.7 Article

Failure to Replicate Genetic Associations with Antidepressant Treatment Response in Duloxetine-Treated Patients

Journal

BIOLOGICAL PSYCHIATRY
Volume 67, Issue 11, Pages 1110-1113

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2009.12.010

Keywords

ABCB1; GRIK4; OPRM1; phosphodiesterases; SLC6A4; SNP

Funding

  1. Lilly and Company
  2. AstraZeneca
  3. Bristol-Myers Squibb
  4. GlaxoSmithKline
  5. Pfizer
  6. Proteus

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Background: Recent studies have identified associations of polymorphisms in several target genes with antidepressant treatment response of serotonin reuptake inhibitors and a tricyclic antidepressant. We sought to replicate these associations in a study of a serotonin-norepinephrine reuptake inhibitor. Methods: In 250 outpatients with nonpsychotic major depressive disorder, response to treatment with once-daily duloxetine (60 mg/day) over 6 weeks was examined for associations with polymorphisms in eight candidate genes previously associated with antidepressant response using mixed-effect model repeated-measures analysis. Treatment response was quantified on the basis of changes from baseline using 17-item Hamilton Depression Rating Scale total scores. Results: Polymorphisms in PDE1A, PDE1C, PDE6A PDE11A, ABCB1, GRIK4, SLC6A4, and OPRM1 genes showed no statistically significant associations (uncorrected, two-tailed p > .05) with duloxetine treatment response. Conclusions: Previously, described associations between polymorphisms in candidate genes and antidepressant treatment response were not replicated in this study. This result may suggest that previous associations are specific to serotonin reuptake inhibitors.

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