Parkinson
Studienlage · Detail RCT · Parkinson · 2024

Short-Term Cannabidiol with Delta-9-Tetrahydrocannabinol in Parkinson's Disease: A Randomized Trial.

Kein Nutzen nachgewiesen GRADE Moderat 19 Zitate
Stichproben = 61 Pat.
Dauer2 Wochen, dann Beobachtung bis…
KontrollePlacebo
EndpunktMDS-UPDRS Motor
Verblindungdoppelblind
DesignRCT
Cannabinoidkombination
THC:CBD1:30
Applikationoral
Kernaussage

CBD/THC zeigte keinen signifikanten Vorteil gegenüber Placebo bei Motor-MDS-UPDRS (Unterschied -1,80, p=0,379); Placebo war möglicherweise überlegen bei Schlaf und Kognition, mit mehr Nebenwirkungen in der CBD/THC-Gruppe.

Zusammenfassung

RCT n=61 (CBD/THC n=31, Placebo n=30), 2 Wochen Titration auf finale Dosis 191,8±48,9 mg CBD + 6,4±1,6 mg THC täglich. Primärer Endpunkt motor MDS-UPDRS: Reduktion -4,57 (95% CI -8,11 bis -1,03; p=0,013) in CBD/THC-Gruppe vs. -2,77 (-4,92 bis -0,61; p=0,014) in Placebo; Gruppen-Differenz nicht signifikant: -1,80 (-5,88 bis 2,27; p=0,379). Kein Benefit, möglicherweise verschlechterte Kognition und Schlaf; starker Placebo-Effekt. Nebenwirkungen mild, häufiger in CBD/THC-Gruppe.

P
PopulationPersonen mit Parkinson-Erkrankung (MDS-UPDRS Motor ≥20, cannabis-naiv), n=61
I
InterventionOrales Cannabis-Extrakt (CBD/THC in Sesamöl), 2,5 mg/kg/Tag, davon ~191,8 mg CBD + 6,4 mg THC täglich, 2 Wochen
C
KontrollePlacebo (orales Sesamöl)
O
OutcomeMotorischer MDS-UPDRS: Reduktion um 4,57 Punkte (CBD/THC) vs. 2,77 Punkte (Placebo); Gruppenunterschied nicht signifikant: −1,80 (95% CI −5,88 bis 2,27; p=0,379)
Vertrauen in die Evidenz
Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

Herabgestuft wegen
Ungenauigkeit
Qualitätsprofil
Größe
Verblindung Doppelblind
Effektstärke Kein Nutzen
Zitate / Jahr
Autoren
Liu Y, Bainbridge J, Sillau S, Rajkovic S, Adkins M, Domen CH, Thompson JA, Seawalt T, Klawitter J, Sempio C
DOI 10.1002/mds.29768
Design: RCT
Teilen
Abstract
Background: Cannabis use is frequent in Parkinson's disease (PD), despite inadequate evidence of benefits and risks. Objective: The aim is to study short-term efficacy and tolerability of relatively high cannabidiol (CBD)/low Delta-9-tetrahydrocannabinol (THC) to provide preliminary data for a longer trial. Methods: Persons with PD with >/=20 on motor Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) who had negative cannabis testing took cannabis extract (National Institute of Drug Abuse) oral sesame oil solution for 2 weeks, increasing to final dose of 2.5 mg/kg/day. Primary outcome was change in motor MDS-UPDRS from baseline to final dose. Results: Participants were randomized to CBD/THC (n = 31) or placebo (n = 30). Mean final dose (CBD/THC group) was 191.8 +/- 48.9 mg CBD and 6.4 +/- 1.6 mg THC daily. Motor MDS-UPDRS was reduced by 4.57 (95% CI, -8.11 to -1.03; P = 0.013) in CBD/THC group, and 2.77 (-4.92 to -0.61; P = 0.014) in placebo; the difference between groups was non-significant: -1.80 (-5.88 to 2.27; P = 0.379). Several assessments had a strong placebo response. Sleep, cognition, and activities of daily living showed a treatment effect, favoring placebo. Overall adverse events were mild and reported more in CBD/THC than placebo group. On 2.5 mg/kg/day CBD plasma level was 54.0 +/- 33.8 ng/mL; THC 1.06 +/- 0.91 ng/mL. Conclusions: The brief duration and strong placebo response limits interpretation of effects, but there was no benefit, perhaps worsened cognition and sleep, and there was many mild adverse events. Longer duration high quality trials that monitor cannabinoid concentrations are essential and would require improved availability of research cannabinoid products in the United States. (c) 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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