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Plasma anandamide concentrations are lower in children with autism spectrum disorder

BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restricted, stereotyped behaviors and impairments in social communication. Although the underlying biological mechanisms of ASD remain poorly understood, recent preclinical research has implicated the endoge...

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Autores principales: Karhson, Debra S., Krasinska, Karolina M., Dallaire, Jamie Ahloy, Libove, Robin A., Phillips, Jennifer M., Chien, Allis S., Garner, Joseph P., Hardan, Antonio Y., Parker, Karen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5848550/
https://www.ncbi.nlm.nih.gov/pubmed/29564080
http://dx.doi.org/10.1186/s13229-018-0203-y
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author Karhson, Debra S.
Krasinska, Karolina M.
Dallaire, Jamie Ahloy
Libove, Robin A.
Phillips, Jennifer M.
Chien, Allis S.
Garner, Joseph P.
Hardan, Antonio Y.
Parker, Karen J.
author_facet Karhson, Debra S.
Krasinska, Karolina M.
Dallaire, Jamie Ahloy
Libove, Robin A.
Phillips, Jennifer M.
Chien, Allis S.
Garner, Joseph P.
Hardan, Antonio Y.
Parker, Karen J.
author_sort Karhson, Debra S.
collection PubMed
description BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restricted, stereotyped behaviors and impairments in social communication. Although the underlying biological mechanisms of ASD remain poorly understood, recent preclinical research has implicated the endogenous cannabinoid (or endocannabinoid), anandamide, as a significant neuromodulator in rodent models of ASD. Despite this promising preclinical evidence, no clinical studies to date have tested whether endocannabinoids are dysregulated in individuals with ASD. Here, we addressed this critical gap in knowledge by optimizing liquid chromatography-tandem mass spectrometry methodology to quantitatively analyze anandamide concentrations in banked blood samples collected from a cohort of children with and without ASD (N = 112). FINDINGS: Anandamide concentrations significantly differentiated ASD cases (N = 59) from controls (N = 53), such that children with lower anandamide concentrations were more likely to have ASD (p = 0.041). In keeping with this notion, anandamide concentrations were also significantly lower in ASD compared to control children (p = 0.034). CONCLUSIONS: These findings are the first empirical human data to translate preclinical rodent findings to confirm a link between plasma anandamide concentrations in children with ASD. Although preliminary, these data suggest that impaired anandamide signaling may be involved in the pathophysiology of ASD.
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spelling pubmed-58485502018-03-21 Plasma anandamide concentrations are lower in children with autism spectrum disorder Karhson, Debra S. Krasinska, Karolina M. Dallaire, Jamie Ahloy Libove, Robin A. Phillips, Jennifer M. Chien, Allis S. Garner, Joseph P. Hardan, Antonio Y. Parker, Karen J. Mol Autism Short Report BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by restricted, stereotyped behaviors and impairments in social communication. Although the underlying biological mechanisms of ASD remain poorly understood, recent preclinical research has implicated the endogenous cannabinoid (or endocannabinoid), anandamide, as a significant neuromodulator in rodent models of ASD. Despite this promising preclinical evidence, no clinical studies to date have tested whether endocannabinoids are dysregulated in individuals with ASD. Here, we addressed this critical gap in knowledge by optimizing liquid chromatography-tandem mass spectrometry methodology to quantitatively analyze anandamide concentrations in banked blood samples collected from a cohort of children with and without ASD (N = 112). FINDINGS: Anandamide concentrations significantly differentiated ASD cases (N = 59) from controls (N = 53), such that children with lower anandamide concentrations were more likely to have ASD (p = 0.041). In keeping with this notion, anandamide concentrations were also significantly lower in ASD compared to control children (p = 0.034). CONCLUSIONS: These findings are the first empirical human data to translate preclinical rodent findings to confirm a link between plasma anandamide concentrations in children with ASD. Although preliminary, these data suggest that impaired anandamide signaling may be involved in the pathophysiology of ASD. BioMed Central 2018-03-12 /pmc/articles/PMC5848550/ /pubmed/29564080 http://dx.doi.org/10.1186/s13229-018-0203-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Karhson, Debra S.
Krasinska, Karolina M.
Dallaire, Jamie Ahloy
Libove, Robin A.
Phillips, Jennifer M.
Chien, Allis S.
Garner, Joseph P.
Hardan, Antonio Y.
Parker, Karen J.
Plasma anandamide concentrations are lower in children with autism spectrum disorder
title Plasma anandamide concentrations are lower in children with autism spectrum disorder
title_full Plasma anandamide concentrations are lower in children with autism spectrum disorder
title_fullStr Plasma anandamide concentrations are lower in children with autism spectrum disorder
title_full_unstemmed Plasma anandamide concentrations are lower in children with autism spectrum disorder
title_short Plasma anandamide concentrations are lower in children with autism spectrum disorder
title_sort plasma anandamide concentrations are lower in children with autism spectrum disorder
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5848550/
https://www.ncbi.nlm.nih.gov/pubmed/29564080
http://dx.doi.org/10.1186/s13229-018-0203-y
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