Metabolic imbalance associated with methylation dysregulation and oxidative damage in children with autism
Open accessAbstract
Oxidative stress and abnormal DNA methylation have been implicated in the pathophysiology of autism. We investigated the dynamics of an integrated metabolic pathway essential for cellular antioxidant and methylation capacity in 68 children with autism, 54 age-matched control children and 40 unaffected siblings. The metabolic profile of unaffected siblings differed significantly from case siblings but not from controls. Oxidative protein/DNA damage and DNA hypomethylation (epigenetic alteration) were found in autistic children but not paired siblings or controls. These data indicate that the deficit in antioxidant and methylation capacity is specific for autism and may promote cellular damage and altered epigenetic gene expression. Further, these results suggest a plausible mechanism by which pro-oxidant environmental stressors may modulate genetic predisposition to autism.
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Several lines of evidence indicate oxidative stress and mitochondrial dysfunction are prevalent in individuals with ASD.
“There are presently several lines of evidence indicating oxidative stress and mitochondrial dysfunction are prevalent in individuals with ASD [3,10,11,12,13,14,15,16].”
From Vitamin D and Autism Spectrum Disorder: A Literature Review (2016) · cites this paper as [14]
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- Authors
- Melnyk, S., Fuchs, G. J., Schulz, E., Lopez, M., Kahler, S. G., Fussell, J. J., Bellando, J., Pavliv, O., Rose, S., Seidel, L., Gaylor, D. W., & Jill James, S.
- Affiliations
- Arkansas Children's Hospital (US)
- University of Arkansas for Medical Sciences (US)
- ORCID
- Venue
- Journal of Autism and Developmental Disorders
- Published
- 2011-04-26
- Volume
- 42
- Issue
- 3
- Pages
- 367-377
- ISSN
- 0162-3257 (ISSN-L)
- 1573-3432
- PMC
- PMC3342663
- OpenAlex
- W2070592913
- Cited by
- 250
- References
- 85
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 11 · 2023: 11 · 2022: 13 · 2021: 15 · 2020: 26 · 2019: 13 · 2018: 24 · 2017: 16 · 2016: 25 · 2015: 17 · 2014: 23 · 2013: 23 · 2012: 13
- FWCI
- 9.58
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Journal of Autism and Developmental Disorders (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Arkansas Biosciences Institute
- National Institutes of Health
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD051873)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- autism spectrum disorder, oxidative stress, DNA methylation, DNA hypomethylation, oxidative protein damage, oxidative DNA damage, antioxidant capacity, metabolic pathways, epigenetic modifications, unaffected siblings, environmental stressors, genetic susceptibility
- MeSH terms
- Autistic Disorder, Child, Child, Preschool, Female, Glutathione, Humans, Male, Case-Control Studies, Reactive Oxygen Species, Oxidative Stress, DNA Methylation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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