Cargando…

No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children

Evaluation of environmental risk factors in the development of autism spectrum disorder (ASD) is needed for a more complete understanding of disease etiology and best approaches for prevention, diagnosis, and treatment. A pilot experiment in 54 children (n = 25 ASD, n = 29 controls; aged 12.4 ± 3.9...

Descripción completa

Detalles Bibliográficos
Autores principales: Duringer, Jennifer, Fombonne, Eric, Craig, Morrie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963856/
https://www.ncbi.nlm.nih.gov/pubmed/27447670
http://dx.doi.org/10.3390/toxins8070224
_version_ 1782444993310359552
author Duringer, Jennifer
Fombonne, Eric
Craig, Morrie
author_facet Duringer, Jennifer
Fombonne, Eric
Craig, Morrie
author_sort Duringer, Jennifer
collection PubMed
description Evaluation of environmental risk factors in the development of autism spectrum disorder (ASD) is needed for a more complete understanding of disease etiology and best approaches for prevention, diagnosis, and treatment. A pilot experiment in 54 children (n = 25 ASD, n = 29 controls; aged 12.4 ± 3.9 years) screened for 87 urinary mycotoxins via liquid chromatography-tandem mass spectrometry to assess current exposure. Zearalenone, zearalenone-4-glucoside, 3-acetyldeoxynivalenol, and altenuene were detected in 9/54 (20%) samples, most near the limit of detection. No mycotoxin/group of mycotoxins was associated with ASD-diagnosed children. To identify potential correlates of mycotoxin presence in urine, we further compared the nine subjects where a urinary mycotoxin was confirmed to the remaining 45 participants and found no difference based on the presence or absence of mycotoxin for age (t-test; p = 0.322), gender (Fisher’s exact test; p = 0.456), exposure or not to selective serotonin reuptake inhibitors (Fisher’s exact test; p = 0.367), or to other medications (Fisher’s exact test; p = 1.00). While no positive association was found, more sophisticated sample preparation techniques and instrumentation, coupled with selectivity for a smaller group of mycotoxins, could improve sensitivity and detection. Further, broadening sampling to in utero (mothers) and newborn-toddler years would cover additional exposure windows.
format Online
Article
Text
id pubmed-4963856
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-49638562016-08-03 No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children Duringer, Jennifer Fombonne, Eric Craig, Morrie Toxins (Basel) Communication Evaluation of environmental risk factors in the development of autism spectrum disorder (ASD) is needed for a more complete understanding of disease etiology and best approaches for prevention, diagnosis, and treatment. A pilot experiment in 54 children (n = 25 ASD, n = 29 controls; aged 12.4 ± 3.9 years) screened for 87 urinary mycotoxins via liquid chromatography-tandem mass spectrometry to assess current exposure. Zearalenone, zearalenone-4-glucoside, 3-acetyldeoxynivalenol, and altenuene were detected in 9/54 (20%) samples, most near the limit of detection. No mycotoxin/group of mycotoxins was associated with ASD-diagnosed children. To identify potential correlates of mycotoxin presence in urine, we further compared the nine subjects where a urinary mycotoxin was confirmed to the remaining 45 participants and found no difference based on the presence or absence of mycotoxin for age (t-test; p = 0.322), gender (Fisher’s exact test; p = 0.456), exposure or not to selective serotonin reuptake inhibitors (Fisher’s exact test; p = 0.367), or to other medications (Fisher’s exact test; p = 1.00). While no positive association was found, more sophisticated sample preparation techniques and instrumentation, coupled with selectivity for a smaller group of mycotoxins, could improve sensitivity and detection. Further, broadening sampling to in utero (mothers) and newborn-toddler years would cover additional exposure windows. MDPI 2016-07-20 /pmc/articles/PMC4963856/ /pubmed/27447670 http://dx.doi.org/10.3390/toxins8070224 Text en © 2016 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 Communication
Duringer, Jennifer
Fombonne, Eric
Craig, Morrie
No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children
title No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children
title_full No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children
title_fullStr No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children
title_full_unstemmed No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children
title_short No Association between Mycotoxin Exposure and Autism: A Pilot Case-Control Study in School-Aged Children
title_sort no association between mycotoxin exposure and autism: a pilot case-control study in school-aged children
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963856/
https://www.ncbi.nlm.nih.gov/pubmed/27447670
http://dx.doi.org/10.3390/toxins8070224
work_keys_str_mv AT duringerjennifer noassociationbetweenmycotoxinexposureandautismapilotcasecontrolstudyinschoolagedchildren
AT fombonneeric noassociationbetweenmycotoxinexposureandautismapilotcasecontrolstudyinschoolagedchildren
AT craigmorrie noassociationbetweenmycotoxinexposureandautismapilotcasecontrolstudyinschoolagedchildren