Studienlage · DetailKlinische Studie · Epilepsie · 2019
Higher cannabidiol plasma levels are associated with better seizure response following treatment with a pharmaceutical grade cannabidiol.
Szaflarski et al.·Epilepsy & behaviorImpact 2.4
Klarer NutzenGRADEModerat78 Zitate
Stichproben = 100 Pat.
Dauerunklar
EndpunktAnfallsfrequenz
Verblindungoffen
DesignKlinische Studie
Cannabinoidcbd
Applikationoral
”Kernaussage
Höhere CBD-Plasmaspiegel sind mit verbesserter Anfallskontrolle assoziiert; ein Anstieg um 100 ng/mL war mit einer Reduktion von etwa 2 Anfällen pro Zeitraum verbunden.
Zusammenfassung
Open-Label EAP mit Epidiolex® bei therapierefraktärer Epilepsie (n=100; 56 Erwachsene, 44 Kinder). Lineare Korrelation zwischen CBD-Dosis (5–50 mg/kg/d) und Plasmaspiegel (7,1–1200 ng/mL; r=0,640, p<0,001). Quantile Regression: 100 ng/mL CBD-Anstieg assoziiert mit ~2 Anfällen weniger pro 2-Wochen-Periode (1,87 [96%-KI 0,34–3,39]; p=0,018). Kinder und Erwachsene zeigten ähnliche Ansprechraten; Kinder möglicherweise responsiv bei niedrigeren Plasmaspiegeln.
P
PopulationErwachsene und Kinder mit therapierefraktärer Epilepsie im Expanded-Access-Programm, n=100 (56 Erwachsene, 44 Kinder, 54 weiblich)
OutcomeLinearer Zusammenhang zwischen CBD-Plasmaspiegeln und Anfallsreduktion: +100 ng/mL CBD-Spiegel assoziiert mit ca. 2 weniger Anfällen pro 2-Wochen-Periode (β=1,87; 96%-KI 0,34–3,39; p=0,018)
Vertrauen in die Evidenz
Sehr niedrigNiedrigModeratHoch
Moderat
Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.
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Verzerrungsrisiko
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VerblindungOffen
EffektstärkeKlarer Nutzen
Zitate / Jahr★★★★★
Autoren
Szaflarski JP, Hernando K, Bebin EM, Gaston TE, Grayson LE, Ampah SB, Moreadith R
Objective: The objective of this study was to determine the relationship between cannabidiol (CBD) dose, CBD plasma level, and seizure control in a large open-label single-center study.
Methods: All participants with treatment-refractory epilepsy participating in our expanded access program (EAP) were approached for participation. Highly purified grade CBD (Epidiolex(R)) dosing was weight-based and could be increased every 2 weeks by 5 mg/kg/day up to a maximum dosage of 50 mg/kg/day depending on tolerance and seizure control. Seizure counts were obtained at each visit with frequency calculated per 2-week periods. Cross-sectional plasma peak levels of CBD were obtained ~4 h after dosing in consecutively presenting patients.
Results: We evaluated 56 adults and 44 children (100 total; 54 female) at two time points - one before initiating CBD and one at the time of CBD plasma level testing. There was a positive linear correlation between CBD dosage (range from 5 to 50 mg/kg/day) and level (range from 7.1-1200 ng/mL) in all participants (r = 0.640; p < 0.001). The quantile regression model supported the notion of increased CBD levels being associated with improvement in seizure frequency after adjusting for age - specifically, a 100 ng/mL increase in CBD level was associated with approximately two counts reduction in seizure frequency per time period (1.87 96% confidence interval [CI] 0.34-3.39; p = 0.018). In participants with the same CBD level, differences in seizure improvement did not depend on age (p = 0.318).
Conclusions: In this open-label study, we found evidence of a linear correlation between CBD dosage and plasma levels, and that higher dose/levels are associated with a higher response rate for seizure improvement. Children and adults responded to CBD similarly. However, seizure control response rates suggest children may respond to lower dosages/plasma levels than adults. Findings reported in this study are specific to Epidiolex(R) and should not be extrapolated to other CBD products.