TY - JOUR
T1 - Exploring cannabidiol effects on inflammatory markers in individuals with cocaine use disorder
T2 - a randomized controlled trial
AU - Morissette, Florence
AU - Mongeau-Pérusse, Violaine
AU - Rizkallah, Elie
AU - Thébault, Paméla
AU - Lepage, Stéphanie
AU - Brissette, Suzanne
AU - Bruneau, Julie
AU - Dubreucq, Simon
AU - Stip, Emmanuel
AU - Cailhier, Jean François
AU - Jutras-Aswad, Didier
N1 - Funding Information:
The Canadian Institutes of Health Research (CIHR) funded this study (#125864). Insys Therapeutics provided the investigational product. DJ-A holds a scholar award from the Fonds de recherche du Québec en Santé. FM received scholarships from the CIHR, the Institut Universitaire sur les Dépendances, the Université de Montréal, and the CRCHUM. JB holds the Canada Research Chair in Addiction Medicine and receives investigator-driven grants from Gilead Sciences and AbbVie for work outside this study.
Funding Information:
We would like to thank the CIHR (#125864), the Fonds de recherche du Québec en Santé, the Université de Montréal, the CRCHUM, the Institut du Cancer de Montréal, and the Institut universitaire sur les dépendances for their financial support. We thank the clinical immunomonitoring core facility of the CRCHUM for performing biobanking, immunophenotyping, and cytokine measurements. We are grateful to Léa Gagnon for reviewing and editing the manuscript, and Guillaume Gazil and his team (Unité de recherche clinique appliquée) for their support in data management and statistical analysis for the main trial. The study team also wants to extend special thanks to all participants for their engagement in this study.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to American College of Neuropsychopharmacology.
PY - 2021/11
Y1 - 2021/11
N2 - Cocaine use disorder (CUD) is a major public health issue associated with physical, social, and psychological problems. Excessive and repeated cocaine use induces oxidative stress leading to a systemic inflammatory response. Cannabidiol (CBD) has gained substantial interest for its anti-inflammatory properties, safety, and tolerability profile. However, CBD anti-inflammatory properties have yet to be confirmed in humans. This exploratory study is based on a single-site randomized controlled trial that enrolled participants with CUD between 18 and 65 years, randomized (1:1) to daily receive either CBD (800 mg) or placebo for 92 days. The trial was divided into a 10-day detoxification (phase I) followed by a 12-week outpatient follow-up (phase II). Blood samples were collected from 48 participants at baseline, day 8, week 4, and week 12 and were analyzed to determine monocytes and lymphocytes phenotypes, and concentrations of various inflammatory markers such as cytokines. We used generalized estimating equations to detect group differences. Participants treated with CBD had lower levels of interleukin-6 (p = 0.017), vascular endothelial growth factor (p = 0.032), intermediate monocytes CD14+CD16+ (p = 0.024), and natural killer CD56negCD16hi (p = 0.000) compared with participants receiving placebo. CD25+CD4+T cells were higher in the CBD group (p = 0.007). No significant group difference was observed for B lymphocytes. This study suggests that CBD may exert anti-inflammatory effects in individuals with CUD.
AB - Cocaine use disorder (CUD) is a major public health issue associated with physical, social, and psychological problems. Excessive and repeated cocaine use induces oxidative stress leading to a systemic inflammatory response. Cannabidiol (CBD) has gained substantial interest for its anti-inflammatory properties, safety, and tolerability profile. However, CBD anti-inflammatory properties have yet to be confirmed in humans. This exploratory study is based on a single-site randomized controlled trial that enrolled participants with CUD between 18 and 65 years, randomized (1:1) to daily receive either CBD (800 mg) or placebo for 92 days. The trial was divided into a 10-day detoxification (phase I) followed by a 12-week outpatient follow-up (phase II). Blood samples were collected from 48 participants at baseline, day 8, week 4, and week 12 and were analyzed to determine monocytes and lymphocytes phenotypes, and concentrations of various inflammatory markers such as cytokines. We used generalized estimating equations to detect group differences. Participants treated with CBD had lower levels of interleukin-6 (p = 0.017), vascular endothelial growth factor (p = 0.032), intermediate monocytes CD14+CD16+ (p = 0.024), and natural killer CD56negCD16hi (p = 0.000) compared with participants receiving placebo. CD25+CD4+T cells were higher in the CBD group (p = 0.007). No significant group difference was observed for B lymphocytes. This study suggests that CBD may exert anti-inflammatory effects in individuals with CUD.
UR - http://www.scopus.com/inward/record.url?scp=85111668661&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85111668661&partnerID=8YFLogxK
U2 - 10.1038/s41386-021-01098-z
DO - 10.1038/s41386-021-01098-z
M3 - Article
C2 - 34331010
AN - SCOPUS:85111668661
SN - 0893-133X
VL - 46
SP - 2101
EP - 2111
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 12
ER -