Study register · detailRCT (double-blind, placebo-controlled) · Addiction · 2024
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 et al.·Molecular PsychiatryImpact 8.0
Clear benefitGRADEModerate14 citations
Samplen = 28 Pat.
DurationSingle dose, follow-up duration…
ControlPlacebo
EndpointNAc activation on fMRI
Blindingdoppelblind
DesignRCT (double-blind, placebo-controlled)
Cannabinoidcbd
Max. dose800.0 mg
Routeoral
”Key finding
CBD group showed significantly lower cue-induced nucleus accumbens activation and significantly less alcohol craving after stress and alcohol cue exposure as well as during the fMRI task compared to placebo.
Summary
n=28 AUD patients, double-blind RCT (ICONIC); CBD 800 mg single dose vs. placebo. CBD reduced bilateral cue-induced nucleus accumbens activation (left: t=4.906, p<0.001, d=1.15; right: t=4.873, p<0.001, d=1.13) as well as alcohol craving after combined stress-/cue-exposure (F=4.516, p=0.043, eta=0.15) and in the fMRI cue-reactivity task (F=6.665, p=0.015, eta=0.23). CBD plasma levels correlated negatively with craving (r=-0.394, p=0.030).
P
PopulationAdults with alcohol use disorder (AUD), n=28
Although alcohol use disorder (AUD) is highly prevalent, only a few medications are approved for its treatment leaving much room for improvement. Cannabidiol (CBD) might be a particularly promising candidate, with preclinical data suggesting that CBD is effective in targeting AUD symptoms and disease processes that drive alcohol use and relapse, due to its anti-craving, stress-reducing, and anti-compulsive effects. Here we report data from the double-blind randomized controlled ICONIC trial that compared the effects of a single dose of 800 mg cannabidiol against placebo (PLC) in N = 28 individuals with AUD. Cue-induced nucleus accumbens (NAc) activation, alcohol craving during a combined stress- and alcohol cue exposure session, as well as craving during an fMRI alcohol cue-reactivity task and CBD plasma levels served as outcomes. Individuals receiving CBD showed lower bilateral cue-induced NAc activation (t = 4.906, p < 0.001, d = 1.15; t = 4.873, p < 0.001, d = 1.13) and reported significantly lower alcohol craving after a combined stress- and alcohol cue exposure session (F = 4.516, p = 0.043, eta = 0.15) and during the fMRI cue-reactivity task (F = 6.665, p = 0.015, eta = 0.23). CBD levels were significantly higher in the CBD group (t = 3.808, p < 0.001, d = 1.47) and showed a significant negative association with alcohol craving during the cue exposure experiment (r = -0.394, p = 0.030) and during fMRI (r = -0.389, p = 0.030), and with left and right NAc activation (r = -0.459, p = 0.030; r = -0.405, p = 0.030). CBD's capacity to reduce stress- and cue-induced alcohol craving and to normalize NAc activation - a region critical to the pathophysiology of AUD - contribute to understanding the neurobiological basis of its clinical effects and support its potential as a treatment option for AUD.