Genome-wide association studies of placebo and duloxetine response in major depressive disorder

M. Maciukiewicz, V. S. Marshe, A. K. Tiwari, T. M. Fonseka, N. Freeman, J. L. Kennedy, S. Rotzinger, J. A. Foster, S. H. Kennedy, D. J. Müller

Research output: Contribution to journalArticlepeer-review

15 Scopus citations


We investigated variants associated with treatment response in depressed patients treated with either the antidepressant duloxetine or placebo using a genome-wide approach. Our sample (N = 391) included individuals aged 18-75 years, diagnosed with major depressive disorder and treated with either duloxetine or placebo for up to 8 weeks. We conducted genome-wide associations for treatment response as operationalized by percentage change in Montgomery-Åsberg Depression Rating Scale score from baseline, as well as mixed models analyses across five time points. In the placebo-treated subsample (N = 205), we observed a genome-wide association with rs76767803 (? = 0.69, P = 1.25 × 10? 8) upstream of STAC1. STAC1 rs76767803 was also associated with response using mixed model analysis (?2 = 3.95; P = 0.001). In the duloxetine-treated subsample (N = 186), we observed suggestive associations with ZNF385D (rs4261893; ? = ? 0.46, P = 1.55 × 10? 5), NCAM1 (rs2303377; ? = 0.45, P = 1.76 × 10? 5) and MLL5 (rs117986340; ? = 0.91, P = 3.04 × 10? 5). Our findings suggest that a variant upstream of STAC1 is associated with placebo response, which might have implications for treatment optimization, clinical trial design and drug development.

Original languageEnglish (US)
Pages (from-to)406-412
Number of pages7
JournalPharmacogenomics Journal
Issue number3
StatePublished - May 22 2018
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Pharmacology


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