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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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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 |
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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 |
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