4.6 Article

EEG Biomarkers to Predict Response to Sertraline and Placebo Treatment in Major Depressive Disorder

期刊

IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING
卷 70, 期 3, 页码 909-919

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IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TBME.2022.3204861

关键词

Electroencephalography; Antidepressants; Depression; Electrodes; Phase measurement; Medical diagnostic imaging; Biomarkers; Directed phase lag index; machine learning; Index Terms; major depressive disorder (MDD); Placebo; predicting response; resting-state electroencephalography (EEG); Sertraline

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This study developed a machine learning algorithm that predicts the effectiveness of antidepressant medications in individual patients using resting EEG data. The algorithm successfully predicted the response to Sertraline or Placebo with over 80% accuracy. This research provides a cost-effective, non-invasive, and easily accessible tool for clinicians to enhance treatment effectiveness, speed up recovery time, reduce personal suffering, and decrease treatment costs.
Objective: Major depressive disorder (MDD) is a persistent psychiatric condition, and the leading cause of disability, affecting up to 5% of the population worldwide. Antidepressant medications (ADMs) are often the first-line treatment for MDD, but it may take the clinician months of trial and error to find an effective ADM for a particular patient. Therefore, identification of predictive biomarkers that can be used to accurately determine the effectiveness of a specific treatment for an individual patient is extremely valuable. Method: Using resting EEG data, we develop a machine learning algorithm (MLA) that searches for connectivity patterns within an individual's EEG signal that are predictive of the probability of responding to the antidepressant Sertraline or Placebo. The MLA has two steps: 1) Directed phase lag index (DPLI), a measure of phase synchronization between brain regions, that is not sensitive to volume conduction is applied to resting-state EEG data, 2) the resulting DPLI matrix is searched for a pattern set of features that can be used to successfully predict the response to Sertraline or Placebo. Results: Our MLA predicted response to Sertraline (N = 105) or Placebo (N = 119) with more than 80% accuracy. Conclusion: Our findings suggest that feature patterns selected from a DPLI matrix may be predictive of response to Sertraline and to Placebo. Significance: The proposed MLA may provide an inexpensive, non-invasive, and readily available tool that clinicians may use to enhance treatment effectiveness, accelerate time to recovery, reduce personal suffering, and decrease treatment costs.

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