4.5 Article

Plasma brain derived neurotrophic factor (BDNF) and response to ketamine in treatment-resistant depression

Journal

INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
Volume 17, Issue 2, Pages 331-336

Publisher

OXFORD UNIV PRESS
DOI: 10.1017/S1461145713001119

Keywords

BDNF; biomarker; depression; ketamine

Funding

  1. National Institutes of Health (NIH)/National Institute of Mental Health (NIMH) [RO1MH081870]
  2. NIH National Center for Advancing Translational Sciences, Department of Veterans Affairs [UL1TR000067]
  3. NARSAD Independent Investigator Award
  4. Career Development Award from NIH/NIMH [1K23MH094707-01]

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Ketamine produces rapid antidepressant effects in treatment-resistant depression (TRD), but the magnitude of response varies considerably between individual patients. Brain-derived neurotrophic factor (BDNF) has been investigated as a biomarker of treatment response in depression and has been implicated in the mechanism of action of ketamine. We evaluated plasma BDNF and associations with symptoms in 22 patients with TRD enrolled in a randomized controlled trial of ketamine compared to an anaesthetic control (midazolam). Ketamine significantly increased plasma BDNF levels in responders compared to non-responders 240min post-infusion, and Montgomery-angstrom sberg Depression Rating Scale (MADRS) scores were negatively correlated with BDNF (r=-0.701, p=0.008). Plasma BDNF levels at 240min post-infusion were highly negatively associated with MADRS scores at 240min (r=-0.897, p=.002), 24h (r=-0.791, p=0.038), 48h (r=-0.944, p=0.001) and 72h (r=-0.977, p=0.010). No associations with BDNF were found for patients receiving midazolam. These data support plasma BDNF as a peripheral biomarker relevant to ketamine antidepressant response.

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