» Articles » PMID: 33884495

FMRI-based Prediction of Naltrexone Response in Alcohol Use Disorder: a Replication Study

Overview
Specialties Neurology
Psychiatry
Date 2021 Apr 22
PMID 33884495
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Pharmacological treatment in alcohol use disorder suffers from modest effect sizes. Efforts have been undertaken to identify patient characteristics that help to select individuals that benefit from pharmacological treatment. Previous studies indicated that neural alcohol cue-reactivity (CR) might provide a marker that identifies patients, which benefit from naltrexone treatment.We investigated the reproducibility of the association between ventral striatum (VS) activation and naltrexone (NTX) treatment response by analyzing data from a recent longitudinal clinical trial in N = 44 abstinent treatment-seeking alcohol-dependent patients. A follow-up was conducted over 3 months. We computed the percentage of significant voxels in VS and tested main effects and interactions with NTX treatment on relapse risk using Cox Regression models.We found a significant interaction effect between pre-treatment cue reactivity in the VS and NTX treatment on time to first heavy relapse (Hazard Ratio = 7.406, 95% CI 1.17-46.56, p = 0.033), such that the patient group with high VS activation (defined by a mean split) showed a significant medication effect (Hazard Ratio = 0.140, 95% CI 0.02-0.75, p = 0.022) with a number needed to treat of 3.4 [95% CI 2.413.5], while there was no significant effect in the group with low VS activation (Hazard Ratio = 0.726, p = 0.454).Thus, using an independent sample we replicated the previously described positive association between VS activation and NTX efficacy. Although our results should be considered cautiously in light of the small sample size, our results support the potential of neural alcohol CR as a tool for precision medicine approaches in alcohol dependence.

Citing Articles

Acute cannabidiol administration reduces alcohol craving and cue-induced nucleus accumbens activation in individuals with alcohol use disorder: the double-blind randomized controlled ICONIC trial.

Zimmermann S, Teetzmann A, Baessler J, Schreckenberger L, Zaiser J, Pfisterer M Mol Psychiatry. 2024; .

PMID: 39668256 DOI: 10.1038/s41380-024-02869-y.


Exploratory study of associations between monetary reward anticipation brain responses and mu-opioid signalling in alcohol dependence, gambling disorder and healthy controls.

Turton S, Paterson L, Myers J, Mick I, Lan C, McGonigle J Neuroimage Rep. 2024; 4(3):100211.

PMID: 39345862 PMC: 11427764. DOI: 10.1016/j.ynirp.2024.100211.


Neuroimaging Biomarkers in Addiction.

Ekhtiari H, Sangchooli A, Carmichael O, Moeller F, ODonnell P, Oquendo M medRxiv. 2024; .

PMID: 39281741 PMC: 11398440. DOI: 10.1101/2024.09.02.24312084.


Parameter Space and Potential for Biomarker Development in 25 Years of fMRI Drug Cue Reactivity: A Systematic Review.

Sangchooli A, Zare-Bidoky M, Fathi Jouzdani A, Schacht J, Bjork J, Claus E JAMA Psychiatry. 2024; 81(4):414-425.

PMID: 38324323 PMC: 11304510. DOI: 10.1001/jamapsychiatry.2023.5483.


The Role of fMRI in Drug Development: An Update.

Carmichael O Adv Neurobiol. 2023; 30:299-333.

PMID: 36928856 DOI: 10.1007/978-3-031-21054-9_13.


References
1.
Lim A, Green R, Grodin E, Venegas A, Meredith L, Donato S . Alcohol Cue-Induced Ventral Striatum Activity Predicts Subsequent Alcohol Self-Administration. Alcohol Clin Exp Res. 2020; 44(6):1224-1233. PMC: 7336863. DOI: 10.1111/acer.14342. View

2.
Witkiewitz K, Roos C, Mann K, Kranzler H . Advancing Precision Medicine for Alcohol Use Disorder: Replication and Extension of Reward Drinking as a Predictor of Naltrexone Response. Alcohol Clin Exp Res. 2019; 43(11):2395-2405. PMC: 6824945. DOI: 10.1111/acer.14183. View

3.
Lukas S, Lowen S, Lindsey K, Conn N, Tartarini W, Rodolico J . Extended-release naltrexone (XR-NTX) attenuates brain responses to alcohol cues in alcohol-dependent volunteers: a bold FMRI study. Neuroimage. 2013; 78:176-85. DOI: 10.1016/j.neuroimage.2013.03.055. View

4.
Hansson A, Grunder G, Hirth N, Noori H, Spanagel R, Sommer W . Dopamine and opioid systems adaptation in alcoholism revisited: Convergent evidence from positron emission tomography and postmortem studies. Neurosci Biobehav Rev. 2018; 106:141-164. DOI: 10.1016/j.neubiorev.2018.09.010. View

5.
Anton R, Oroszi G, OMalley S, Couper D, Swift R, Pettinati H . An evaluation of mu-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence: results from the Combined Pharmacotherapies and Behavioral Interventions for Alcohol Dependence (COMBINE) study. Arch Gen Psychiatry. 2008; 65(2):135-44. PMC: 2666924. DOI: 10.1001/archpsyc.65.2.135. View