TY - JOUR
T1 - The medial forebrain bundle as a deep brain stimulation target for treatment resistant depression
T2 - A review of published data
AU - Gálvez, Juan F.
AU - Keser, Zafer
AU - Mwangi, Benson
AU - Ghouse, Amna A.
AU - Fenoy, Albert J.
AU - Schulz, Paul E.
AU - Sanches, Marsal
AU - Quevedo, Joao
AU - Selvaraj, Sudhakar
AU - Gajwani, Prashant
AU - Zunta-Soares, Giovana
AU - Hasan, Khader M.
AU - Soares, Jair C.
N1 - Funding Information:
Dr. Marsal Sanches has served on the speakers' bureau for AstraZeneca and has received grant support from Janssen.
Funding Information:
This work was partly funded by the Dunn Research Foundation (Houston, TX) and Pat Rutherford, Jr Chair in Psychiatry (UTHealth) 73C-1-8585 .
Publisher Copyright:
© 2014 Elsevier Inc.
PY - 2015/4/3
Y1 - 2015/4/3
N2 - Introduction: Despite a wide variety of therapeutic interventions for major depressive disorder (MDD), treatment resistant depression (TRD) remains to be prevalent and troublesome in clinical practice. In recent years, deep brain stimulation (DBS) has emerged as an alternative for individuals suffering from TRD not responding to combining antidepressants, multiple adjunctive strategies and electroconvulsive therapy (ECT). Although the best site for TRD-DBS is still unclear, pilot data suggests that the medial forebrain bundle (MFB) might be a key target to accomplish therapeutic efficacy in TRD patients. Objective: To explore the anatomic, electrophysiologic, neurocognitive and treatment data supporting the MFB as a target for TRD-DBS. Results: The MFB connects multiple targets involved in motivated behavior, mood regulation and antidepressant response. Specific phenomenology associated with TRD can be linked specifically to the superolateral branch (sl) of the MFB (slMFB). TRD patients who received DBS-slMFB reported high response/remission rates with an improvement in functioning and no significant adverse outcomes in their physical health or neurocognitive performance. Discussion: The slMFB is an essential component of a network of structural and functional pathways connecting different areas possibly involved in the pathogenesis of mood disorders. Therefore, the slMFB should be considered as an exciting therapeutic target for DBS therapy to achieve a sustained relief in TRD patients. Conclusion: There is an urgent need for clinical trials exploring DBS-slMFB in TRD. Further efforts should pursue measuring baseline pro-inflammatory cytokines, oxidative stress, and cognition as possible biomarkers of DBS-slMFB response in order to aid clinicians in better patient selection.
AB - Introduction: Despite a wide variety of therapeutic interventions for major depressive disorder (MDD), treatment resistant depression (TRD) remains to be prevalent and troublesome in clinical practice. In recent years, deep brain stimulation (DBS) has emerged as an alternative for individuals suffering from TRD not responding to combining antidepressants, multiple adjunctive strategies and electroconvulsive therapy (ECT). Although the best site for TRD-DBS is still unclear, pilot data suggests that the medial forebrain bundle (MFB) might be a key target to accomplish therapeutic efficacy in TRD patients. Objective: To explore the anatomic, electrophysiologic, neurocognitive and treatment data supporting the MFB as a target for TRD-DBS. Results: The MFB connects multiple targets involved in motivated behavior, mood regulation and antidepressant response. Specific phenomenology associated with TRD can be linked specifically to the superolateral branch (sl) of the MFB (slMFB). TRD patients who received DBS-slMFB reported high response/remission rates with an improvement in functioning and no significant adverse outcomes in their physical health or neurocognitive performance. Discussion: The slMFB is an essential component of a network of structural and functional pathways connecting different areas possibly involved in the pathogenesis of mood disorders. Therefore, the slMFB should be considered as an exciting therapeutic target for DBS therapy to achieve a sustained relief in TRD patients. Conclusion: There is an urgent need for clinical trials exploring DBS-slMFB in TRD. Further efforts should pursue measuring baseline pro-inflammatory cytokines, oxidative stress, and cognition as possible biomarkers of DBS-slMFB response in order to aid clinicians in better patient selection.
KW - Deep brain stimulation (DBS)
KW - Medial forebrain bundle (MFB)
KW - Neuromodulation
KW - Psychiatry
KW - Treatment resistance depression (TRD)
UR - http://www.scopus.com/inward/record.url?scp=84920111160&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84920111160&partnerID=8YFLogxK
U2 - 10.1016/j.pnpbp.2014.12.003
DO - 10.1016/j.pnpbp.2014.12.003
M3 - Review article
C2 - 25530019
AN - SCOPUS:84920111160
VL - 58
SP - 59
EP - 70
JO - Progress in Neuro-Psychopharmacology and Biological Psychiatry
JF - Progress in Neuro-Psychopharmacology and Biological Psychiatry
SN - 0278-5846
ER -