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
Klarer NutzenGRADEModerat14 Zitate
Stichproben = 28 Pat.
DauerEinzeldosis…
KontrollePlacebo
EndpunktNAc-Aktivierung im fMRT
Verblindungdoppelblind
DesignRCT (double-blind, placebo-controlled)
Cannabinoidcbd
Max. Dosis800.0 mg
Applikationoral
”Kernaussage
CBD-Gruppe zeigte signifikant niedrigere cue-induzierte nucleus accumbens Aktivierung und signifikant geringeres Alkoholverlangen nach Stress- und Alkohol-Cue-Exposition sowie während fMRI-Task im Vergleich zu Placebo.
Zusammenfassung
n=28 AUD-Patienten, doppelblinde RCT (ICONIC); CBD 800 mg Einzeldosis vs. Placebo. CBD reduzierte beidseitige cue-induzierte Nucleus-accumbens-Aktivierung (links: t=4.906, p<0.001, d=1.15; rechts: t=4.873, p<0.001, d=1.13) sowie Alkohol-Craving nach kombinierter Stress-/Cue-Exposition (F=4.516, p=0.043, eta=0.15) und im fMRI-Cue-Reaktivitäts-Task (F=6.665, p=0.015, eta=0.23). CBD-Plasmaspiegel korrelierten negativ mit Craving (r=-0.394, p=0.030).
P
PopulationErwachsene mit Alkoholgebrauchsstörung (AUD), n=28
OutcomeSignifikant reduzierte bilaterale Nucleus-accumbens-Aktivierung (t=4.906/4.873, p<0.001, d=1.15/1.13), reduziertes Craving nach Stress-/Cue-Exposition (F=4.516, p=0.043, η=0.15) und im fMRT (F=6.665, p=0.015, η=0.23) unter CBD vs. Placebo
Vertrauen in die Evidenz
Sehr niedrigNiedrigModeratHoch
Moderat
Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.
Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe★★★★★
VerblindungDoppelblind
EffektstärkeKlarer Nutzen
Zitate / Jahr★★★★★
Autoren
Zimmermann S, Teetzmann A, Baessler J, Schreckenberger L, Zaiser J, Pfisterer M, Stenger M, Bach P
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.