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Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials
BACKGROUND: The prevalence of cannabis use and cannabis use disorders (CUD) has significantly increased over time. However, there are no approved pharmacological treatments for CUD. The aim of this study was to determine the efficacy and safety of various medical cannabinoids in the treatment of CUD...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256935/ https://www.ncbi.nlm.nih.gov/pubmed/35815028 http://dx.doi.org/10.3389/fpsyt.2022.867878 |
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author | Vuilleumier, Caroline Scherbaum, Norbert Bonnet, Udo Roser, Patrik |
author_facet | Vuilleumier, Caroline Scherbaum, Norbert Bonnet, Udo Roser, Patrik |
author_sort | Vuilleumier, Caroline |
collection | PubMed |
description | BACKGROUND: The prevalence of cannabis use and cannabis use disorders (CUD) has significantly increased over time. However, there are no approved pharmacological treatments for CUD. The aim of this study was to determine the efficacy and safety of various medical cannabinoids in the treatment of CUD. METHODS: We conducted a systematic review of randomized controlled trials which evaluated the therapeutic potential of medical cannabinoids in individuals with CUD and summarized the main study outcomes in terms of cannabis use, abstinence, withdrawal symptoms, craving, retention in treatment and adverse events. RESULTS: We identified eight trials with a total of 667 study participants. Dronabinol reduced cannabis withdrawal symptoms whereas nabiximols, cannabidiol and PF-04457845, a fatty acid amide inhibitor, also reduced cannabis use and improved abstinence, compared to placebo. Nabilone failed to demonstrate efficacy in the treatment of CUD. All medications were well-tolerated. CONCLUSIONS: Cannabinoid receptor agonists, i.e., dronabinol and nabilone, showed only limited or no therapeutic potential in the treatment of CUD. In contrast, modulators of endocannabinoid activity, i.e., nabiximols, cannabidiol and PF-04457845, demonstrated broader efficacy which covered almost all aspects of CUD. Endocannabinoid modulation appears to be a promising treatment approach in CUD, but the evidence to support this strategy is still small and future research in this direction is needed. |
format | Online Article Text |
id | pubmed-9256935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92569352022-07-07 Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials Vuilleumier, Caroline Scherbaum, Norbert Bonnet, Udo Roser, Patrik Front Psychiatry Psychiatry BACKGROUND: The prevalence of cannabis use and cannabis use disorders (CUD) has significantly increased over time. However, there are no approved pharmacological treatments for CUD. The aim of this study was to determine the efficacy and safety of various medical cannabinoids in the treatment of CUD. METHODS: We conducted a systematic review of randomized controlled trials which evaluated the therapeutic potential of medical cannabinoids in individuals with CUD and summarized the main study outcomes in terms of cannabis use, abstinence, withdrawal symptoms, craving, retention in treatment and adverse events. RESULTS: We identified eight trials with a total of 667 study participants. Dronabinol reduced cannabis withdrawal symptoms whereas nabiximols, cannabidiol and PF-04457845, a fatty acid amide inhibitor, also reduced cannabis use and improved abstinence, compared to placebo. Nabilone failed to demonstrate efficacy in the treatment of CUD. All medications were well-tolerated. CONCLUSIONS: Cannabinoid receptor agonists, i.e., dronabinol and nabilone, showed only limited or no therapeutic potential in the treatment of CUD. In contrast, modulators of endocannabinoid activity, i.e., nabiximols, cannabidiol and PF-04457845, demonstrated broader efficacy which covered almost all aspects of CUD. Endocannabinoid modulation appears to be a promising treatment approach in CUD, but the evidence to support this strategy is still small and future research in this direction is needed. Frontiers Media S.A. 2022-06-22 /pmc/articles/PMC9256935/ /pubmed/35815028 http://dx.doi.org/10.3389/fpsyt.2022.867878 Text en Copyright © 2022 Vuilleumier, Scherbaum, Bonnet and Roser. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Vuilleumier, Caroline Scherbaum, Norbert Bonnet, Udo Roser, Patrik Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials |
title | Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials |
title_full | Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials |
title_fullStr | Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials |
title_full_unstemmed | Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials |
title_short | Cannabinoids in the Treatment of Cannabis Use Disorder: Systematic Review of Randomized Controlled Trials |
title_sort | cannabinoids in the treatment of cannabis use disorder: systematic review of randomized controlled trials |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256935/ https://www.ncbi.nlm.nih.gov/pubmed/35815028 http://dx.doi.org/10.3389/fpsyt.2022.867878 |
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