Literature DB >> 29087373

Deep brain stimulation for treatment-resistant major depressive disorder: a comparison of two targets and long-term follow-up.

S Raymaekers1,2, L Luyten3,4, C Bervoets2, L Gabriëls2, B Nuttin3,5.   

Abstract

We previously found that electrical stimulation in the anterior limb of the internal capsule/bed nucleus of the stria terminalis (IC/BST) alleviates depressive symptoms in severe treatment-resistant obsessive-compulsive disorder (OCD) patients. Here we tested the hypothesis that electrical stimulation in either IC/BST or in the inferior thalamic peduncle (ITP) effectively reduces depressive symptoms in treatment-resistant major depressive disorder (TRD). In a double-blind crossover design, the effects of electrical stimulation at both targets were compared in TRD patients. The 17-item Hamilton Depression Rating scale (HAM-D) was the primary outcome measure. During the first crossover, patients received IC/BST stimulation versus no stimulation in random order (2 × 1 weeks). During the second crossover (3 × 2 months), patients received IC/BST versus ITP versus no stimulation. Patients and evaluators were blinded for stimulation conditions. All patients (n=7) were followed up for at least 3 years (3-8 years) after implantation. Six patients completed the first crossover and five patients completed the second. During the first crossover, mean (s.d.) HAM-D scores were 21.5 (2.7) for no stimulation and 11.5 (8.8) for IC/BST stimulation. During the second crossover, HAM-D scores were 15.4 (7.5) for no stimulation, 7.6 (3.8) for IC/BST stimulation and 11.2 (7.5) for ITP stimulation. The final sample size was too small to statistically analyze this second crossover. At last follow-up, only one patient preferred ITP over IC/BST stimulation. Two patients, with a history of suicide attempts before implantation, committed suicide during the follow-up phases of this study. Our data indicate that, in the long term, both ITP and IC/BST stimulation may alleviate depressive symptoms in patients suffering from TRD.

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Year:  2017        PMID: 29087373      PMCID: PMC5682606          DOI: 10.1038/tp.2017.66

Source DB:  PubMed          Journal:  Transl Psychiatry        ISSN: 2158-3188            Impact factor:   6.222


  48 in total

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2.  Long-term effects of nucleus accumbens deep brain stimulation in treatment-resistant depression: evidence for sustained efficacy.

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4.  Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication.

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5.  Multiple recurrences of major depressive disorder.

Authors:  D A Solomon; M B Keller; A C Leon; T I Mueller; P W Lavori; M T Shea; W Coryell; M Warshaw; C Turvey; J D Maser; J Endicott
Journal:  Am J Psychiatry       Date:  2000-02       Impact factor: 18.112

6.  Deep brain stimulation for treatment-refractory obsessive-compulsive disorder: psychopathological and neuropsychological outcome in three cases.

Authors:  L Gabriëls; P Cosyns; B Nuttin; H Demeulemeester; J Gybels
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9.  Deep brain stimulation of the ventral capsule/ventral striatum for treatment-resistant depression.

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10.  Neuropsychological outcome after deep brain stimulation in the ventral capsule/ventral striatum for highly refractory obsessive-compulsive disorder or major depression.

Authors:  Cynthia S Kubu; Donald A Malone; Gordon Chelune; Paul Malloy; Ali R Rezai; Tom Frazier; Andre Machado; Steven Rasmussen; Gerhard Friehs; Benjamin D Greenberg
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Journal:  Mol Psychiatry       Date:  2018-02-27       Impact factor: 15.992

Review 4.  Invasive Brain Stimulation in the Treatment of Psychiatric Illness–Proposed Indications and Approaches.

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6.  Integrating Brain Implants With Local and Distributed Computing Devices: A Next Generation Epilepsy Management System.

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8.  Long-term deep brain stimulation of the ventral anterior limb of the internal capsule for treatment-resistant depression.

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Review 9.  Corticotropin Releasing Hormone Signaling in the Bed Nuclei of the Stria Terminalis as a Link to Maladaptive Behaviors.

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10.  A Systematic Review of Neuromodulation Treatment Effects on Suicidality.

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