Modulation of neural oscillations in escitalopram treatment: a Canadian biomarker integration network in depression study
- PMID: 39396045
- PMCID: PMC11470922
- DOI: 10.1038/s41398-024-03110-8
Modulation of neural oscillations in escitalopram treatment: a Canadian biomarker integration network in depression study
Abstract
Current pharmacological agents for depression have limited efficacy in achieving remission. Developing and validating new medications is challenging due to limited biological targets. This study aimed to link electrophysiological data and symptom improvement to better understand mechanisms underlying treatment response. Longitudinal changes in neural oscillations were assessed using resting-state electroencephalography (EEG) data from two Canadian Biomarker Integration Network in Depression studies, involving pharmacological and cognitive behavioral therapy (CBT) trials. Patients in the pharmacological trial received eight weeks of escitalopram, with treatment response defined as ≥ 50% decrease in Montgomery-Åsberg Depression Rating Scale (MADRS). Early (baseline to week 2) and late (baseline to week 8) changes in neural oscillation were investigated using relative power spectral measures. An association was found between an initial increase in theta and symptom improvement after 2 weeks. Additionally, late increases in delta and theta, along with a decrease in alpha, were linked to a reduction in MADRS after 8 weeks. These late changes were specifically observed in responders. To assess specificity, we extended our analysis to the independent CBT cohort. Responders exhibited an increase in delta and a decrease in alpha after 2 weeks. Furthermore, a late (baseline to week 16) decrease in alpha was associated with symptom improvement following CBT. Results suggest a common late decrease in alpha across both treatments, while modulatory effects in theta may be specific to escitalopram treatment. This study offers insights into electrophysiological markers indicating a favorable response to antidepressants, enhancing our comprehension of treatment response mechanisms in depression.
© 2024. The Author(s).
Conflict of interest statement
T.A.A. was supported by NIMH Grant No. K01-MH123915. P.B. has received consulting and speaking honoraria from AbbVie, Allergan, Eisai, Janssen, Lundbeck, Merck, Pfizer, Otsuka, and research grants from CAN-BIND, CIHR, Janssen, OBI and Otsuka. J.A.F. has served on the Scientific Advisory Board for MRM Health NL and has received consulting/speaker fees from Alphasights, Novozymes, Klaire Labs, Takeda Canada, Rothman, Benson, Hedges Inc., and WebMD. S.K. reports grants from the Labatt Family Innovation Fund in Brain Health (Department of Psychiatry, University of Toronto), the Max Bell Foundation, the Canadian Centre on Substance Use and Addiction, the Ontario Ministry of Health and Long-Term Care (MOHLTC), and the Canadian Institutes of Health Research (CIHR). S.K. has received honorarium for past consultation from EmpowerPharm. R.W.L. has received honoraria for ad hoc speaking or advising/consulting, or received research funds, from: Asia-Pacific Economic Cooperation, BC Leading Edge Foundation, Canadian Institutes of Health Research, Canadian Network for Mood and Anxiety Treatments, Grand Challenges Canada, Healthy Minds Canada, Janssen, Lundbeck, Lundbeck Institute, Medscape, Michael Smith Foundation for Health Research, MITACS, Myriad Neuroscience, Ontario Brain Institute, Otsuka, Pfizer, Sanofi, Unity Health, Vancouver Coastal Health Research Institute, and VGH-UBCH Foundation. R.M. has received consulting and speaking honoraria from AbbVie, Allergan, Eisai, Janssen, KYE, Lallemand, Lundbeck, Neonmind, Otsuka, and Sunovion, and research grants from CAN-BIND, CIHR, Janssen, Lallemand, Lundbeck, Nubiyota, OBI and OMHF. C.N.S. reported receiving personal fees from Otsuka and Sunovion and grants from Ontario Brain Institute, SEAMO Innovation Funds, and Ontario Research Fund–Research Excellence outside the submitted work. D.J.M. reports grants from the Canadian Institutes of Health Research (CIHR) and the Alternative Funding Plan (CAMH-AFP). D.J.M. has received a speaker honorarium rom Novagenic. S.R. reported receiving grants from Ontario Brain Institute and the Canadian Institutes of Health Research during the conduct of the study and having a patent to Teneurin C-Terminal Associated Peptides and Methods and Uses Thereof issued. S.H.K. - Grant received/grants pending - Abbott, Allergan, Brain Canada, Canadian Institutes for Health Research (CIHR), Janssen, Lundbeck, Ontario Brain Institute, Ontario Research Fund (ORF), Otsuka, Pfizer, Servier, Sunovion and Xian-Janssen. Consulting fees or honorarium - Abbott, Alkermes, Allergan, Boehringer Ingelheim, Brain Canada, Canadian Institutes for Health Research (CIHR), Janssen, Lundbeck, Lundbeck Institute, Ontario Brain Institute, Ontario Research. Stock/Stock Options – Field Trip Health. F.F. reported receiving funding from Michael Smith Foundation for Health Research, Natural Sciences and Engineering Research Council of Canada Discovery, and Canadian Institutes of Health Research. All other authors report no biomedical financial interests or potential conflicts of interest.
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References
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- World Health Organization. Depression and Other Common Mental Disorders Global Health Estimates. (2017).
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