Deep brain stimulation of the nucleus accumbens/ventral capsule for severe and intractable opioid and benzodiazepine use disorder.


Journal

Experimental and clinical psychopharmacology
ISSN: 1936-2293
Titre abrégé: Exp Clin Psychopharmacol
Pays: United States
ID NLM: 9419066

Informations de publication

Date de publication:
Apr 2021
Historique:
entrez: 27 5 2021
pubmed: 28 5 2021
medline: 8 6 2021
Statut: ppublish

Résumé

Given high relapse rates and the prevalence of overdose deaths, novel treatments for substance use disorder (SUD) are desperately needed for those who are treatment refractory. The objective of this study was to evaluate the safety of deep brain stimulation (DBS) for SUD and the effects of DBS on substance use, substance craving, emotional symptoms, and frontal/executive functions. DBS electrodes were implanted bilaterally within the Nucleus Accumbens/Ventral anterior internal capsule (NAc/VC) of a man in his early 30s with >10-year history of severe treatment refractory opioid and benzodiazepine use disorders. DBS of the NAc/VC was found to be safe with no serious adverse events noted and the participant remained abstinent and engaged in comprehensive treatment at the 12-week endpoint (and 12-month extended follow-up). Using a 0-100 visual analog scale, substance cravings decreased post-DBS implantation; most substantially in benzodiazepine craving following the final DBS titration (1.0 ± 2.2) compared to baseline (53.4 ± 29.5; p < .001). A trend toward improvement in frontal/executive function was observed on the balloon analog risk task performance following the final titration (217.7 ± 76.2) compared to baseline (131.3 ± 28.1, p = .066). FDG PET demonstrated an increase in glucose metabolism in the dorsolateral prefrontal and medial premotor cortices at the 12-week endpoint compared to post-surgery/pre-DBS titration. Heart Rate Variability (HRV) improved following the final titration (rMSSD = 56.0 ± 11.7) compared to baseline (19.2 ± 8.2; p < .001). In a participant with severe, treatment refractory opioid and benzodiazepine use disorder, DBS of the NAc/VC was safe, reduced substance use and craving, and improved frontal and executive functions. Confirmation of these findings with future studies is needed. (PsycInfo Database Record (c) 2021 APA, all rights reserved).

Identifiants

pubmed: 34043402
pii: 2021-49902-005
doi: 10.1037/pha0000453
pmc: PMC8422285
mid: NIHMS1735202
doi:

Substances chimiques

Analgesics, Opioid 0
Benzodiazepines 12794-10-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

210-215

Subventions

Organisme : NIGMS NIH HHS
ID : U54 GM104942
Pays : United States
Organisme : NIDA NIH HHS
ID : UG3 DA047714
Pays : United States
Organisme : NIH HHS
Pays : United States

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Auteurs

James J Mahoney (JJ)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

Marc W Haut (MW)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

Sally L Hodder (SL)

West Virginia Clinical and Translational Science Institute, WVUSOM.

Wanhong Zheng (W)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

Laura R Lander (LR)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

James H Berry (JH)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

Daniel L Farmer (DL)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

Jennifer L Marton (JL)

Department of Behavioral Medicine and Psychiatry, Department of Neuroscience, Rockefeller Neuroscience Institute (RNI), West Virginia University School of Medicine (WVUSOM).

Manish Ranjan (M)

Department of Neurosurgery, Department of Neuroscience, RNI, WVUSOM.

Nicholas J Brandmeir (NJ)

Department of Neurosurgery, Department of Neuroscience, RNI, WVUSOM.

Victor S Finomore (VS)

Department of Neuroscience, RNI, WVUSOM.

Jeremy L Hensley (JL)

Department of Anesthesiology, WVUSOM.

Will M Aklin (WM)

National Institutes of Health, National Institute on Drug Abuse.

Gene-Jack Wang (GJ)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism.

Dardo Tomasi (D)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism.

Ehsan Shokri-Kojori (E)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism.

Ali R Rezai (AR)

Department of Neurosurgery, Department of Neuroscience, RNI, WVUSOM.

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