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Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder
Autism spectrum disorder (ASD) is a behaviorally defined disorder which has increased in prevalence over the last two decades. Despite decades of research, no effective treatment is currently available. Animal models, as well as other lines of evidence, point to abnormalities in the balance of corti...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025936/ https://www.ncbi.nlm.nih.gov/pubmed/24872724 http://dx.doi.org/10.2147/DHPS.S39595 |
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author | Frye, Richard E |
author_facet | Frye, Richard E |
author_sort | Frye, Richard E |
collection | PubMed |
description | Autism spectrum disorder (ASD) is a behaviorally defined disorder which has increased in prevalence over the last two decades. Despite decades of research, no effective treatment is currently available. Animal models, as well as other lines of evidence, point to abnormalities in the balance of cortical excitation to inhibition in individuals with ASD, with this imbalance resulting in an overall increase in cortical excitation. To reduce cortical excitatory glutamate pathways, arbaclofen, a selective agonist of the gamma aminobutyric acid receptor type B, has been developed. This article reviews the evidence for this treatment for ASD using a systematic review methodology. Overall, a systematic search of the literature revealed 148 relevant references with the majority of these being review papers or news items that mentioned the potential promise of arbaclofen. Five original studies were identified, four of which used STX209, a form of arbaclofen developed by Seaside Therapeutics, Inc., and one which used R-baclofen. In an animal model, treatment of Fragile X, a genetic disease with ASD features, demonstrated a reversal of behavioral, neurological, and neuropathological features associated with the disease. One double-blind, placebo-controlled study treated children and adults with Fragile X. Results from this study were promising, with signs of improvement in social function, especially in the most severely socially impaired. Two studies, one open-label and one double-blind, placebo-controlled, were conducted in children, adolescents, and young adults with ASD. These studies suggested some improvements in socialization, although the effects were limited and may have been driven by individuals with ASD that were higher-functioning. These studies and others that have used arbaclofen for the treatment of gastroesophageal reflux suggest that arbaclofen is safe and well-tolerated. Clearly, further clinical studies are needed in order to refine the symptoms and characteristics of children with ASD that are best treated with arbaclofen. |
format | Online Article Text |
id | pubmed-4025936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40259362014-05-28 Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder Frye, Richard E Drug Healthc Patient Saf Review Autism spectrum disorder (ASD) is a behaviorally defined disorder which has increased in prevalence over the last two decades. Despite decades of research, no effective treatment is currently available. Animal models, as well as other lines of evidence, point to abnormalities in the balance of cortical excitation to inhibition in individuals with ASD, with this imbalance resulting in an overall increase in cortical excitation. To reduce cortical excitatory glutamate pathways, arbaclofen, a selective agonist of the gamma aminobutyric acid receptor type B, has been developed. This article reviews the evidence for this treatment for ASD using a systematic review methodology. Overall, a systematic search of the literature revealed 148 relevant references with the majority of these being review papers or news items that mentioned the potential promise of arbaclofen. Five original studies were identified, four of which used STX209, a form of arbaclofen developed by Seaside Therapeutics, Inc., and one which used R-baclofen. In an animal model, treatment of Fragile X, a genetic disease with ASD features, demonstrated a reversal of behavioral, neurological, and neuropathological features associated with the disease. One double-blind, placebo-controlled study treated children and adults with Fragile X. Results from this study were promising, with signs of improvement in social function, especially in the most severely socially impaired. Two studies, one open-label and one double-blind, placebo-controlled, were conducted in children, adolescents, and young adults with ASD. These studies suggested some improvements in socialization, although the effects were limited and may have been driven by individuals with ASD that were higher-functioning. These studies and others that have used arbaclofen for the treatment of gastroesophageal reflux suggest that arbaclofen is safe and well-tolerated. Clearly, further clinical studies are needed in order to refine the symptoms and characteristics of children with ASD that are best treated with arbaclofen. Dove Medical Press 2014-05-10 /pmc/articles/PMC4025936/ /pubmed/24872724 http://dx.doi.org/10.2147/DHPS.S39595 Text en © 2014 Frye. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Frye, Richard E Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
title | Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
title_full | Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
title_fullStr | Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
title_full_unstemmed | Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
title_short | Clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
title_sort | clinical potential, safety, and tolerability of arbaclofen in the treatment of autism spectrum disorder |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025936/ https://www.ncbi.nlm.nih.gov/pubmed/24872724 http://dx.doi.org/10.2147/DHPS.S39595 |
work_keys_str_mv | AT fryericharde clinicalpotentialsafetyandtolerabilityofarbaclofeninthetreatmentofautismspectrumdisorder |