Microstructural changes in deep gray nuclei following electroconvulsive therapy.

Authors

Christopher G Filippi, Matthew Yh Leung, Aziz M Ulug, Artemis Zavaliangos-Petropulu, Richard Watts

Published in

AJNR. American journal of neuroradiology. Sep 29, 2026. Epub Sep 29, 2026.

Abstract

Electroconvulsive therapy (ECT) is efficacious for the treatment of major depressive disorder. However, its underlying mechanism of action remains debated and may involve neurogenesis, changes in axon/synaptic density or glial cells. Restriction spectrum imaging (RSI) is an MRI technique that can resolve subvoxel microstructure, separating intracellular water from extracellular water, which can be further partitioned into hindered and free water. This technique can be used to determine whether ECT affects cellular microstructure through changes in signal contributions. In the present study, we aim to determine how RSI metrics change following ECT and whether these metrics correlate with clinical improvement.
RSI analysis of the Perturbation of Depression Connectome (PDC 1.0) diffusion MRI data for healthy control and predominantly right unilateral ECT patients. MRI studies were undertaken at baseline, 1-week post-treatment and 3-months post ECT (follow-up).
Following ECT, right-sided RSI metrics changed in cortical and subcortical brain regions including right amygdala and right hippocampus between baseline and post-treatment. The hindered water compartment increased, the free water compartment decreased, and the intracellular compartment was unchanged. Post-treatment, volume increased in the amygdala and hippocampus, which partially resolved at follow-up, while right amygdala extracellular indices persisted. Changes in clinical symptoms did not clearly relate to volumetric or diffusion changes.
RSI provides imaging biomarkers that suggest extracellular water shifts with corresponding volume changes to be the predominant effect of ECT. Transient and longer-term changes in glymphatic flow may be one of the contributing, underlying mechanisms of action for ECT.

PMID:
42810830
Bibliographic data and abstract were imported from PubMed on 30 Sep 2026.

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