Brain derived neurotrophic factor (BDNF) and autism spectrum disorders (ASD) in childhood
Abstract
Background Neurotrophic factors are essential regulators of neuronal maturation including synaptic synthesis. Among those, Brain derived neurotrophic factor (BDNF) has been in particular focus in the understanding of autism spectrum disorders (ASD).Purpose The aim of our study was to investigate whether BNDF could be used as diagnostic/biological marker for ASD. For this purpose we examined the plasma levels of BDNF and the precursors pro- BDNF in patients with ASD and compared it with non-autistic controls; determined whether there was a correlation between the BDNF and proBDNF levels and clinical severity. We also investigated the coding region of BDNF identify for well-variations which could be associated to ASD.Methods The 65 ASD patients (51 boys) were enrolled from a recent completed epidemiological survey covering two counties (Oppland and Hedmark) in Norway. The mean age of the total number of children who participated in this study was 11,7 years. 30 non-autistic children were included as controls, 14 boys and 16 girls. The mean age was 11.3 years. Exclusion criteria for control group were individuals suffering from either neurological, endocrine, or immune insuffiency.Results and conclusions Patients with ASD were characterized by moderately but significantly elevated plasma levels of BDNF compared to matched controls. No differences were observed in the proBDNF level between patients and controls. Within the ASD group, children with intellectual disability demonstrated increased BDNF, but not proBDNF levels, while the presence of ADHD had no impact on circulating proBDNF or BDNF. No further associations between plasma proBDNF or BDNF and other clinical demographics were observed.
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When examined in older children (4 and 11 years of age), serum levels of BDNF are elevated in children with ASD versus neurotypical controls.
“However, when examined in older children (4 and 11 years of age), serum levels of BDNF are elevated in children with ASD versus neurotypical controls [ 165 , 166 ].”
From DNA methylation: a mechanism linking environmental chemical exposures to risk of autism spectrum disorders? (2016) · cites this paper as [165]
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References 24 · Cited by 83
- Authors
- Bryn, V., Halvorsen, B., Ueland, T., Isaksen, J., Kolkova, K., Ravn, K., & Skjeldal, O. H.
- Affiliations
- Innlandet Hospital Trust (NO)
- Oslo University Hospital (NO)
- Copenhagen University Hospital (DK)
- University of Gothenburg (SE)
- Corresponding author
- Bryn, V.
- Venue
- European Journal of Paediatric Neurology
- Publisher
- Elsevier BV
- Published
- 2015-07
- Volume
- 19
- Issue
- 4
- Pages
- 411-414
- ISSN
- 1090-3798 (ISSN-L)
- OpenAlex
- W2149290119
- Cited by
- 83
- References
- 24
- Citations by year
- 2026: 14 · 2025: 7 · 2024: 7 · 2023: 8 · 2022: 7 · 2021: 9 · 2020: 4 · 2019: 2 · 2018: 7 · 2017: 5 · 2016: 11 · 2015: 2
- FWCI
- 5.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Paediatric Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Psychiatry and Mental health › Child Nutrition and Feeding Issues
- Keywords
- brain-derived neurotrophic factor, autism spectrum disorder, proBDNF, plasma biomarkers, diagnostic biomarkers, intellectual disability, ADHD comorbidity, clinical severity, children
- MeSH terms
- Autism Spectrum Disorder, Adolescent, Child, Demography, Female, Humans, Male, Norway, Biomarkers, Brain-Derived Neurotrophic Factor
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