Subanesthetic ketamine alters EEG signal complexity: Implications for treatment stratification in depression
Language English Country Netherlands Media print-electronic
Document type Controlled Clinical Trial, Journal Article
PubMed
40419149
DOI
10.1016/j.jad.2025.119477
PII: S0165-0327(25)00919-X
Knihovny.cz E-resources
- Keywords
- Biomarker, EEG, Ketamine, Lempel-Ziv complexity, MDD, Treatment response,
- MeSH
- Excitatory Amino Acid Antagonists * administration & dosage pharmacology MeSH
- Depressive Disorder, Treatment-Resistant * drug therapy physiopathology MeSH
- Depressive Disorder, Major * drug therapy physiopathology MeSH
- Adult MeSH
- Double-Blind Method MeSH
- Electroencephalography * drug effects MeSH
- Ketamine * administration & dosage pharmacology therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Brain * drug effects physiopathology MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Controlled Clinical Trial MeSH
- Names of Substances
- Excitatory Amino Acid Antagonists * MeSH
- Ketamine * MeSH
Major depressive disorder, particularly its treatment-resistant form (TRD), poses significant treatment challenges. Ketamine, an N-methyl-d-aspartate receptor antagonist, has shown promise in rapidly alleviating depressive symptoms by influencing neuroplasticity and glutamatergic modulation, which are thought to influence brain activity complexity. In this placebo-controlled study, we examined the effects of subanesthetic doses of intravenous ketamine on EEG signal complexity in 24 MDD patients, 21 of whom had TRD. Treatment response was defined by a ≥ 33 % reduction in Montgomery-Åsberg Depression Rating Scale (MADRS) after ketamine administration. Patients underwent eyes-closed resting state EEG recording pre-, start-, end- and 24 h post-infusion, analyzed for temporospatial and spatiotemporal Lempel-Ziv complexity (LZCT and LZCS). Results indicated that ketamine significantly increased whole-brain LZCT during infusion compared to placebo (sodium chloride 0.9 %) (16.90 % vs. -4.84 %, 95 % CI 4.29 to 39.18, p = 0.017). Elevated LZCT at end-pre was associated with less short-term symptom improvement the following day. Conversely, lower pretreatment occipital LZCT (0.33 vs. 0.46, 95 % CI 0.007 to 0.26, p = 0.040) predicted a favorable response to ketamine, supported by a logistic regression model with an ROC area of 0.75. No significant changes were observed in LZCS, suggesting limited utility as a biomarker. In conclusion, occipital LZCT could serve as an effective predictive biomarker for ketamine's therapeutic effects in MDD, with implications for patients with TRD. This underscores the potential of EEG complexity measures in stratifying treatment and enhancing our understanding of the neural impacts of ketamine in depressive disorders.
Centre for Cognitive and Brain Sciences University of Macau Taipa Macau
Hospital for Psychiatry Psychotherapy and Psychosomatic; University Zurich Zurich Switzerland
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