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Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies

The etiopathogenesis of autism spectrum disorder (ASD) remains largely unclear. Among other biological hypotheses, researchers have evidenced an imbalance in the endocannabinoid (eCB) system, which regulates some functions typically impaired in ASD, such as emotional responses and social interaction...

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Autores principales: Fusar-Poli, Laura, Cavone, Vito, Tinacci, Silvia, Concas, Ilaria, Petralia, Antonino, Signorelli, Maria Salvina, Díaz-Caneja, Covadonga M., Aguglia, Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563787/
https://www.ncbi.nlm.nih.gov/pubmed/32825313
http://dx.doi.org/10.3390/brainsci10090572
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author Fusar-Poli, Laura
Cavone, Vito
Tinacci, Silvia
Concas, Ilaria
Petralia, Antonino
Signorelli, Maria Salvina
Díaz-Caneja, Covadonga M.
Aguglia, Eugenio
author_facet Fusar-Poli, Laura
Cavone, Vito
Tinacci, Silvia
Concas, Ilaria
Petralia, Antonino
Signorelli, Maria Salvina
Díaz-Caneja, Covadonga M.
Aguglia, Eugenio
author_sort Fusar-Poli, Laura
collection PubMed
description The etiopathogenesis of autism spectrum disorder (ASD) remains largely unclear. Among other biological hypotheses, researchers have evidenced an imbalance in the endocannabinoid (eCB) system, which regulates some functions typically impaired in ASD, such as emotional responses and social interaction. Additionally, cannabidiol (CBD), the non-intoxicating component of Cannabis sativa, was recently approved for treatment-resistant epilepsy. Epilepsy represents a common medical condition in people with ASD. Additionally, the two conditions share some neuropathological mechanisms, particularly GABAergic dysfunctions. Hence, it was hypothesized that cannabinoids could be useful in improving ASD symptoms. Our systematic review was conducted according to the PRISMA guidelines and aimed to summarize the literature regarding the use of cannabinoids in ASD. After searching in Web of Knowledge(TM), PsycINFO, and Embase, we included ten studies (eight papers and two abstracts). Four ongoing trials were retrieved in ClinicalTrials.gov. The findings were promising, as cannabinoids appeared to improve some ASD-associated symptoms, such as problem behaviors, sleep problems, and hyperactivity, with limited cardiac and metabolic side effects. Conversely, the knowledge of their effects on ASD core symptoms is scarce. Interestingly, cannabinoids generally allowed to reduce the number of prescribed medications and decreased the frequency of seizures in patients with comorbid epilepsy. Mechanisms of action could be linked to the excitatory/inhibitory imbalance found in people with ASD. However, further trials with better characterization and homogenization of samples, and well-defined outcomes should be implemented.
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spelling pubmed-75637872020-10-27 Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies Fusar-Poli, Laura Cavone, Vito Tinacci, Silvia Concas, Ilaria Petralia, Antonino Signorelli, Maria Salvina Díaz-Caneja, Covadonga M. Aguglia, Eugenio Brain Sci Review The etiopathogenesis of autism spectrum disorder (ASD) remains largely unclear. Among other biological hypotheses, researchers have evidenced an imbalance in the endocannabinoid (eCB) system, which regulates some functions typically impaired in ASD, such as emotional responses and social interaction. Additionally, cannabidiol (CBD), the non-intoxicating component of Cannabis sativa, was recently approved for treatment-resistant epilepsy. Epilepsy represents a common medical condition in people with ASD. Additionally, the two conditions share some neuropathological mechanisms, particularly GABAergic dysfunctions. Hence, it was hypothesized that cannabinoids could be useful in improving ASD symptoms. Our systematic review was conducted according to the PRISMA guidelines and aimed to summarize the literature regarding the use of cannabinoids in ASD. After searching in Web of Knowledge(TM), PsycINFO, and Embase, we included ten studies (eight papers and two abstracts). Four ongoing trials were retrieved in ClinicalTrials.gov. The findings were promising, as cannabinoids appeared to improve some ASD-associated symptoms, such as problem behaviors, sleep problems, and hyperactivity, with limited cardiac and metabolic side effects. Conversely, the knowledge of their effects on ASD core symptoms is scarce. Interestingly, cannabinoids generally allowed to reduce the number of prescribed medications and decreased the frequency of seizures in patients with comorbid epilepsy. Mechanisms of action could be linked to the excitatory/inhibitory imbalance found in people with ASD. However, further trials with better characterization and homogenization of samples, and well-defined outcomes should be implemented. MDPI 2020-08-20 /pmc/articles/PMC7563787/ /pubmed/32825313 http://dx.doi.org/10.3390/brainsci10090572 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fusar-Poli, Laura
Cavone, Vito
Tinacci, Silvia
Concas, Ilaria
Petralia, Antonino
Signorelli, Maria Salvina
Díaz-Caneja, Covadonga M.
Aguglia, Eugenio
Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies
title Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies
title_full Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies
title_fullStr Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies
title_full_unstemmed Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies
title_short Cannabinoids for People with ASD: A Systematic Review of Published and Ongoing Studies
title_sort cannabinoids for people with asd: a systematic review of published and ongoing studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563787/
https://www.ncbi.nlm.nih.gov/pubmed/32825313
http://dx.doi.org/10.3390/brainsci10090572
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