Hippocampal Gray Volumes Increase in Treatment-Resistant Depression Responding to Vagus Nerve Stimulation.

J ECT

From the *Department of Neurosciences, Section of Psychiatry, University-Hospital of Padova, Padova; †Casa di Cura Parco dei Tigli, Teolo, Padova; ‡Department of Psychiatry, ULSS 6, Padova; §Department of Psychiatry, ULSS 2, Treviso; ∥Private Practitioner in Psychiatry, Padova; and ¶Neurosurgery Unit, #Neuroradiology Unit, and **Section of Neurology, Department of Neurosciences, University-Hospital of Padova, Padova, Italy.

Published: September 2017

AI Article Synopsis

  • Changes in hippocampal gray matter volumes are linked to major depressive disorder and its treatment, particularly in treatment-resistant cases.
  • This study evaluated 6 patients with treatment-resistant depression before and after 6 and 12 months of vagus nerve stimulation, measuring hippocampal volumes and depression severity.
  • Results showed significant increases in hippocampal volumes and improvements in depression scores, suggesting that vagus nerve stimulation positively impacts hippocampal plasticity and may be an effective treatment for those with treatment-resistant depression.

Article Abstract

Background: Changes in hippocampal gray matter volumes are proposed to be involved in pathogenesis, course, and treatment response of major depressive disorder. Converging evidence suggests that reduced neurogenesis may occur in treatment-resistant depression (TRD). Vagus nerve stimulation (VNS) is a well-defined, long-term brain stimulation treatment for TRD. However, its in vivo positive effect on hippocampal modulation as mechanism of action has never been investigated before in clinical studies. In this study, we intended to explore hippocampal volumetric changes and clinical antidepressant responses in patients with TRD after 6 and 12 months of treatment with VNS.

Methods: The TRD outpatients were evaluated for VNS implantation. Right and left hippocampal volumes in 6 TRD patients, who met the criteria for VNS treatment, were measured at baseline before the implantation and after 6 and 12 months. The patients were assessed using Beck Depression Inventory and Hamilton Depression Rating Scale at baseline and at follow-up visits.

Results: There was a statistically significant and progressive increase in right and left hippocampal volumes during the follow up (P < 0.05). Furthermore, patients showed a significant improvement on Hamilton Depression Rating Scale and Beck Depression Inventory scores (P < 0.05).

Conclusions: Our data suggest a VNS modulatory effect on hippocampal plasticity as measured by hippocampal gray volume increase in TRD patients. These preliminary findings indicate the fundamental role of hippocampal remodeling as a marker of response to VNS in TRD.

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Source
http://dx.doi.org/10.1097/YCT.0000000000000424DOI Listing

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