Department of Psychiatry, Yale University School of Medicine, New Haven, United States; Department of Psychiatry, Psychotherapy and Psychosomatics, University Hospital for Psychiatry Zurich, Zurich, Switzerland
Interdepartmental Neuroscience Program, Yale University, New Haven, United States
Aleksandar Savic
Department of Psychiatry, University of Zagreb, Zagreb, Croatia
Nicole Santamauro
Department of Psychiatry, Yale University School of Medicine, New Haven, United States
Zailyn Tamayo
Department of Psychiatry, Yale University School of Medicine, New Haven, United States
Caroline Diehl
Department of Psychology, University of California, Los Angeles, Los Angeles, United States
Antonija Kolobaric
Center of Neuroscience, University of Pittsburgh, Pittsburgh, United States
Morgan Flynn
Department of Psychiatry, Vanderbilt University Medical Center, Nashville, United States
Nathalie Rieser
Department of Psychiatry, Psychotherapy and Psychosomatics, University Hospital for Psychiatry Zurich, Zurich, Switzerland
Clara Fonteneau
Department of Psychiatry, Yale University School of Medicine, New Haven, United States
Terry Camarro
Magnetic Resonance Research Center, Yale University School of Medicine, New Haven, United States
Junqian Xu
Department of Radiology and Psychiatry, Baylor College of Medicine, Houston, United States
Youngsun Cho
Department of Psychiatry, Yale University School of Medicine, New Haven, United States; Child Study Center, Yale University School of Medicine, New Haven, United States
Grega Repovs
Department of Psychology, University of Ljubljana, Ljubljana, Slovenia
Sarah K Fineberg
Department of Psychiatry, Yale University School of Medicine, New Haven, United States
Peter T Morgan
Department of Psychiatry, Yale University School of Medicine, New Haven, United States; Department of Psychiatry, Bridgeport Hospital, Bridgeport, United States
Erich Seifritz
Department of Psychiatry, Psychotherapy and Psychosomatics, University Hospital for Psychiatry Zurich, Zurich, Switzerland
Department of Psychiatry, Yale University School of Medicine, New Haven, United States; Department of Physics, Yale University, Boston, United States; Department of Psychology, Yale University, New Haven, United States
Department of Psychiatry, Yale University School of Medicine, New Haven, United States; Department of Psychiatry, Psychotherapy and Psychosomatics, University Hospital for Psychiatry Zurich, Zurich, Switzerland
Department of Psychiatry, Yale University School of Medicine, New Haven, United States; Interdepartmental Neuroscience Program, Yale University, New Haven, United States
Background: Ketamine has emerged as one of the most promising therapies for treatment-resistant depression. However, inter-individual variability in response to ketamine is still not well understood and it is unclear how ketamine’s molecular mechanisms connect to its neural and behavioral effects. Methods: We conducted a single-blind placebo-controlled study, with participants blinded to their treatment condition. 40 healthy participants received acute ketamine (initial bolus 0.23 mg/kg, continuous infusion 0.58 mg/kg/hr). We quantified resting-state functional connectivity via data-driven global brain connectivity and related it to individual ketamine-induced symptom variation and cortical gene expression targets. Results: We found that: (i) both the neural and behavioral effects of acute ketamine are multi-dimensional, reflecting robust inter-individual variability; (ii) ketamine’s data-driven principal neural gradient effect matched somatostatin (SST) and parvalbumin (PVALB) cortical gene expression patterns in humans, while the mean effect did not; and (iii) behavioral data-driven individual symptom variation mapped onto distinct neural gradients of ketamine, which were resolvable at the single-subject level. Conclusions: These results highlight the importance of considering individual behavioral and neural variation in response to ketamine. They also have implications for the development of individually precise pharmacological biomarkers for treatment selection in psychiatry. Funding: This study was supported by NIH grants DP5OD012109-01 (A.A.), 1U01MH121766 (A.A.), R01MH112746 (J.D.M.), 5R01MH112189 (A.A.), 5R01MH108590 (A.A.), NIAAA grant 2P50AA012870-11 (A.A.); NSF NeuroNex grant 2015276 (J.D.M.); Brain and Behavior Research Foundation Young Investigator Award (A.A.); SFARI Pilot Award (J.D.M., A.A.); Heffter Research Institute (Grant No. 1–190420) (FXV, KHP); Swiss Neuromatrix Foundation (Grant No. 2016–0111) (FXV, KHP); Swiss National Science Foundation under the framework of Neuron Cofund (Grant No. 01EW1908) (KHP); Usona Institute (2015 – 2056) (FXV). Clinical trial number: NCT03842800