Cognitive functioning following long-term cannabidiol use in adults with treatment-resistant epilepsy.


Journal

Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858

Informations de publication

Date de publication:
08 2019
Historique:
received: 17 11 2018
revised: 22 04 2019
accepted: 24 04 2019
pubmed: 21 6 2019
medline: 24 7 2020
entrez: 21 6 2019
Statut: ppublish

Résumé

Cognitive dysfunction is a common comorbidity in adults with treatment-resistant epilepsy (TRE). Recently, cannabidiol (CBD) has demonstrated efficacy in epilepsy treatment. However, our understanding of CBD's cognitive effects in epilepsy is limited. We examined long-term cognitive effects of CBD in adults with TRE as part of an ongoing prospective, open-label safety study. Twenty-sevenadults with TRE (mean age: 34[SD +14], female 52%) enrolled in the UAB CBD program completed standardized cognitive testing (NIH Toolbox Cognition Battery (NIHTB-CB)) at pre-CBD administration baseline and at one-yearfollow-up. Participants were receiving stable CBD dose at the time of one-year testing (mean=36.5mg/kg/day). The NIHTB-CB consisted of two global composite scales (Fluid and Crystallized) and seven individual tests measuring aspects of working memory, episodic memory, executive function, processing speed, and language. All participants had recorded Chalfont Seizure Severity Scale (CSSS) scores at each visit. Statistical analyses consisted of t-test, Pearson correlation coefficient, and linear regression. At baseline, cognitive test performance was below average for both global composite scales (Fluid: 71 [±18] range: 46-117) and Crystallized (76 [±15] range: 59-112)]. Longitudinal analysis revealed no significant group change across the two global composite scales. Of the seven individual cognitive tests, none changed significantly over time. No correlation was found between the cognitive change scores and CBD dose (all P's≥0.21). Change in cognitive test performance was not associated change in seizure severity rating. These findings are encouraging and indicate that long-term administration of pharmaceutical grade CBD is overall cognitively well-tolerated in adults with TRE.

Identifiants

pubmed: 31220785
pii: S1525-5050(18)30931-4
doi: 10.1016/j.yebeh.2019.04.044
pii:
doi:

Substances chimiques

Cannabidiol 19GBJ60SN5

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105-110

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Roy C Martin (RC)

University of Alabama at Birmingham, Department of Neurology, Birmingham, AL, USA. Electronic address: rmartin@uabmc.edu.

Tyler E Gaston (TE)

University of Alabama at Birmingham, Department of Neurology, Birmingham, AL, USA; Birmingham VA Medical Center, Birmingham, AL, USA.

Matthew Thompson (M)

Children's Hospital of Alabama, Birmingham, AL, USA.

Steve B Ampah (SB)

University of Alabama at Birmingham, Department of Biostatistics, Birmingham, AL, USA.

Gary Cutter (G)

University of Alabama at Birmingham, Department of Biostatistics, Birmingham, AL, USA.

E Martina Bebin (EM)

University of Alabama at Birmingham, Department of Neurology, Birmingham, AL, USA.

Jerzy P Szaflarski (JP)

University of Alabama at Birmingham, Department of Neurology, Birmingham, AL, USA.

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Classifications MeSH