4.7 Article

Immediate cerebral metabolic changes induced by discontinuation of deep brain stimulation of subcallosal cingulate gyrus in treatment-resistant depression

Journal

JOURNAL OF AFFECTIVE DISORDERS
Volume 173, Issue -, Pages 159-162

Publisher

ELSEVIER
DOI: 10.1016/j.jad.2014.10.035

Keywords

Deep brain stimulation; Treatment-resistant depression; Positron emission tomography

Funding

  1. Fondo de Investigacion Sanitaria from the Instituto de Salud Carlos III [FIS: PI 10/00372, PI 06/0662, PS 09/00580]
  2. Centro de Investigacion Biomedica en Red de Salad Mental (CIBERSAM)
  3. Agencia de Gestio d'Ajuts Universitaris i de Recerca of the Generalitat de Catalunya
  4. Instituto de Salad Carlos III
  5. Ministerio de Ciencia e Innovacion of the Spanish Government
  6. Instituto de Investigacion Carlos III [CP10-00393]
  7. European Regional Development Fund (ERDF)

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Background: Positron emission tomography (PET) studies have shown that the antidepressant effect of chronic deep brain stimulation (DBS) of the subcallosal cingulate gyrus (SCG) may be consequence of modifications of brain metabolism at key structures involved in depression. Like clinical benefits, these metabolic changes may reverse when the stimulation is discontinued, even preceding clinical worsening. However no data on immediate effects of DBS discontinuation are available. The aim of this study was to determine immediate cerebral metabolism changes during a short switch-off of electrical stimulation in implanted patients with treatment-resistant depression (TRD) who had achieved clinical improvement after a period of chronic DBS. Methods: Seven patients with TRD who had been previously implanted for DBS in SCG were included. After a period of clinical stabilization two consecutive FOG-PET were acquired, the first with active stimulation and the second after 48 h of inactive stimulation. A HAMD-17 to assess depressive symptoms was performed before both scans. Analyses were performed with SnPM8. Results: Inactive stimulation was characterized by metabolism decreases in dorsal anterior cingulate (Broadmann Area, BA24), premotor region (BA6) and putamen with respect to active stimulation. No clinical changes according to HAMD-17 were detected. Limitations: The main limitation of this study is the small sample size. Conclusion: Our results point to immediate effects of DOS discontinuation on metabolism of brain depressive network which precede clinical changes, helping to disentangle the rationale behind DBS efficacy in TRD. (C)2014 Elsevier By. All rights reserved,

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