Pediatric Traumatic Brain Injury And Autism

  • Kay Taylor Masters in Science and Health Communication – University of Dundee

Get health & wellness advice into your inbox

Your privacy is important to us. Any information you provide to us via this website may be placed by us on servers. If you do not agree to these placements, please do not provide the information.

Best Milk Alternative

Introduction

Research into Pediatric Traumatic Brain Injury (TBI) and Autism Spectrum Disorder (ASD) has led scientists to the conclusion that TBIs may potentially result in ASD, as severe head injury can result in the neural rewiring of the brain. Even without a diagnosis of ASD, TBI and ASD, patients still exhibit many of the shared symptoms.1

Pediatric TBI occurs when children have head trauma, resulting in internal injury. This can often lead to temporary/ or permanent disability and or even death in children. Disabilities from TBIs can be physical as well as but also intellectual disabilities.2

ASD is a developmental intellectual disability that manifests during early childhood. It often limits an individuals' social understanding and capabilities, with a host of positive and negative symptoms that can differ from patient to patient. There is no definitive cause, and many environmental and genetic factors are predicted to be responsible for the disorder.3,7

In this article, I will discuss the connection between the two, how TBIs can lead to an increased risk of ASD, and what to do if you are concerned about your child. 

TBIs and ASD

TBI in children should be quickly identified and treated to minimise the risk of further injury and disability. Once the physical examination has occurred and the patient is deemed safe, a neurological exam is next to observe any changes in behaviour and function to determine if there is damage to neurological and cognitive function.4 Injuries of the brain can lead to dysfunction and negative symptoms dependent on location and severity, causing disability either physical, mental, emotional etc. This is due to the damage of neurons preventing correct signalling.1

TBI at key developmental stages in a child's life can cause lasting effects that may be permanent, such as during birth or early childhood. Damage can lead to disability manifesting at a young age, and often requires behavioural and cognitive therapies to maintain normal behaviours.5 Children who have suffered a TBI have a more likely chance of being diagnosed with ASD and ADHD later in life, this chance increasing with increased TBIs either from accidents or abuse. This is one of the outcomes of long-term disability that may occur as a result of TBIs.3,6 There are many other long-lasting outcomes possible depending on the injury. 

ASD manifests symptoms as early as 14 months old,7 but the changes in neural wiring occur as early as the 2nd and 3rd trimesters.8,10 The differential wiring maintains itself throughout early development, persisting until adulthood.6

Symptoms of ASD include: 

  • Communication and language deficits 
  • Repetitive and irregular behaviour
  • Limited interests

Other symptoms can include: 

  • Increased anxiety 
  • Issues with emotional regulation and recognition 
  • Impaired executive function 

Each selection and severity of symptoms differ between individuals with ASD, resulting in a spectrum of results.2,7

The cause of ASD has not been uncovered as of yet. There is much research into genetic causes, and certain genes have been identified, but it is presumed that it is the result of many different genes having small effects to lead to the large effect that is ASD. Environmental factors such as maternal smoking during pregnancy have also been observed to have an effect on development, but it is not stated to be the primary cause of ASD.9

Connection and causation

The primary feature of ASD at a cellular level is that the neurons in the brain are rewired differently from that of a neurotypical brain. Rewiring is the result of genetic risks mutations, and environmental stressors.6,10 leading to incorrect signalling from cells and endogenous neuromodulators that occurs during prenatal and early development,11 leading to both increased and decreased synapse formation depending on the area of the brain.3,8,10 One key area found to be affected is the cerebellum, a key factor in the development of social capabilities after birth.3  

TBI results in neuronal damage, which results in the loss of synapses in the damaged area through microglia.12 However, moderate or severe head injuries at key points of development - up to 3 years old - at targeted brain areas are associated with the over-activation of microglia and influencing the genetic factors and their expression leading to ASD-like symptoms.13 A primary area that when injured may result in ASD is the cerebellum.3

Changes to the cerebellum can lead to downstream changes in the structure of various areas associated with ASD, such as the hippocampus, amygdala, inferior temporal cortex & frontal neocortical areas.3,8,10 The downstream effects in various areas are due to the long-distance loops it shares with many areas of the brain. Interruption of these loops can cause mismatched electrochemical firing of neurons and result in many different symptoms across brain structures. Issues with wiring from the cerebellum are present within ASD individuals and are thought to also be present in certain TBI patients.3,8

Why does it have such a prolonged effect? 

TBI at early ages can cause changes in the stress hormone, cell signalling factors and genetic expression.5,12,14 These changes can result in different neuron attachments and changes in DNA expression, causing a change in wiring that is maintained. The change in neuronal wiring can cause symptoms like communication and social issues similar to that of ASD. The chemical and structural changes are also similar to ASD.5

Symptoms and diagnosis

If a child has a severe head collision, medical diagnosis should be sought out immediately to prevent any further internal or external injury. If the injury is internal, there is a higher chance of prolonged effects, some of which may be disabilities.1,4

After a TBI, children should be closely monitored for any abnormal changes in behaviour.1,5 Diagnosis of ASD and ADHD is external to the TBI treatment and should be sought out if deemed necessary, as the symptoms of such will not appear for some time after the injury.6

ASD-like symptoms that arise as a result of TBIs show similar developmental issues as that of ASD and are frequently diagnosed as such, regardless of history.13

ASD diagnosis is an extended process that involves monitoring the patient for key behaviours, such as reduced eye contact, peculiar and repetitive behaviour, and reduced social interactions.2 ASD children often miss key stages of development and social milestones, such as knowing the appropriate situational facial expressions and not sharing or showing interests with others.15

Does TBI cause ASD?

This question comes down to the semantics of what is considered ASD or not. ASD developmental issues occur before birth and the changes are enacted throughout development post-birth. TBIs are environmental factors that cause changes during or after birth that result in ASD-like symptoms, hence developmental changes. TBIs can be deemed an environmental factor associated with ASD or a separate entity itself due to the lateness of the changes seen.

Regardless of what is considered, children with ASD symptoms - genetic or environmental - will develop differently from neurotypical children. Despite the differences in causality, they have similar symptoms,3,5 can be diagnosed the same,13 will face similar challenges and require similar care.5 Perhaps they are different, but it does not help to differentiate between the two when it comes to the patients themselves.

Care

Care for ASD has been difficult due to the various areas that are affected, the lack of understanding of the disorder itself, and no real way to prevent the development of the disorder. To deal with severe symptoms that affect day-to-day life medications can be described depending on the symptom being managed, such as attention problems, or depression.2,5

Current therapies focus on cognitive behavioural therapy (CBT) to help manage the behavioural symptoms of ASD. By taking part in CBT, ASD individuals can learn to manage negative symptoms more carefully to prevent large outbursts, meltdowns, and aggressive behaviour toward others and themselves, and improve communication and social capabilities.2

A large factor in ASD is understanding of the disorder. There are things which maybe can be learned, but often ASD individuals struggle with or cannot help many of their behaviours. This makes it difficult to communicate ways to understand or assist with what is happening or intentions that can help with interactions and socializing. With ASD diagnosis becoming normalised within society accommodations can be put in place to assist with anything they may struggle with. Symptoms can be shared but each ASD individual is different and often requires unique care, which should be discussed with either the individual or carers of individuals.2

TBI care immediately after is either short-term or long-term. They may suffer from memory issues and issues with balance and motor functions temporarily and may require assistance with basic tasks until symptoms pass. This assistance can be found through rehabilitation therapies to help achieve daily functions, such as strengthening, speech practice, and psychological and cognitive therapy.1,4

Care for disabilities that occur as a result of TBIs is dependent on the nature of the disability, and advice should be sought out from a medical professional. In terms of intellectual disabilities, diagnosis and appropriate care for ASD and ADHD as detailed above is the ideal route for providing a child with the best care.

Summary

TBIs in children can result in temporary issues with many aspects of life, moderate and severe injuries leading to possible life-long disabilities. Young children, up to 3 years old, with TBIs have an increased chance of being diagnosed with ASD and ADHD, a developmental disorder affecting social capability and brain functions.

Differences between TBI-causing ASD-like symptoms and ASD without TBIs are non-significant and require similar care, understanding individual needs at the centre of proper care.

FAQs

Can you gain ASD from a TBI in later life?

No, due to the nature of the disability, it cannot be gained once the brain has developed past a certain point. Damage to neurons in later life will destroy those neurons/synapses, and regrowth will occur when necessary. It does not change the development of an adult as it can in children, as those structures are already in place.

What are the benefits of ASD diagnosis?

Benefits are unique to the individual. Sometimes diagnosis can help confirm suspicions and give closure to the patient and their carers. It can help put in place accommodations to help their day-to-day life and receive help in personal and professional environments. Individuals may not necessarily benefit from a diagnosis and don’t deem it necessary to determine if they are. A diagnosis should happen to help the ASD individual live a comfortable life in a society that isn’t tailored to them.

References

  1. Wang SS, Kloth AD, Badura A. The cerebellum, sensitive periods, and autism. Neuron. 2014 Aug 6;83(3):518-32. doi: 10.1016/j.neuron.2014.07.016. PMID: 25102558; PMCID: PMC4135479.
  2. Araki T, Yokota H, Morita A. Pediatric Traumatic Brain Injury: Characteristic Features, Diagnosis, and Management. Neurol Med Chir (Tokyo). 2017 Feb 15;57(2):82-93. doi: 10.2176/nmc.ra.2016-0191. Epub 2017 Jan 20. PMID: 28111406; PMCID: PMC5341344.
  3. National Institute of Mental Health, Autism Spectrum Disorder, U.S. Department of Health and Human Services, National Institutes of Health, URL: https://www.nimh.nih.gov/health/topics/autism-spectrum-disorders-asd, Retrieved: 06/2024.
  4. Brain Trauma Foundation; American Association of Neurological Surgeons; Congress of Neurological Surgeons. Guidelines for the management of severe traumatic brain injury. J Neurotrauma. 2007;24 Suppl 1:S1-106. doi: 10.1089/neu.2007.9999. Erratum in: J Neurotrauma. 2008 Mar;25(3):276-8. PMID: 17511534.
  5. Singh R, Turner RC, Nguyen L, Motwani K, Swatek M, Lucke-Wold BP. Pediatric Traumatic Brain Injury and Autism: Elucidating Shared Mechanisms. Behav Neurol. 2016;2016:8781725. doi: 10.1155/2016/8781725. Epub 2016 Dec 15. Erratum in: Behav Neurol. 2017;2017:5652160. PMID: 28074078; PMCID: PMC5198096.
  6. Porter, Melanie, Sindella Sugden-Lingard, Ruth Brunsdon, and Suzanne Benson. 2023. "Autism Spectrum Disorder in Children with an Early History of Paediatric Acquired Brain Injury" Journal of Clinical Medicine 12, no. 13: 4361. https://doi.org/10.3390/jcm12134361
  7. M. Kopanska, D. Ochojska, A. Banas-Zabczyk, M. Sochocka, M. Ochnik, S. Torices, R.C. Morgan, J. Leszek, J. Podgorska-Bednarz8, J. Szczygielski, Brain as the house of autistic soul: Current trends in analyzing the risk factors and building up the diagnosis in mild forms of autism spectrum disorder. Journal of Physiology and Pharmacology 2021, 72, 6 www.jpp.krakow.pl | DOI: 10.26402/jpp.2021.6.01
  8. Beopoulos A, Géa M, Fasano A, Iris F. Autism spectrum disorders pathogenesis: Toward a comprehensive model based on neuroanatomic and neurodevelopment considerations. Front Neurosci. 2022 Nov 3;16:988735. doi: 10.3389/fnins.2022.988735. PMID: 36408388; PMCID: PMC9671112.
  9. Rylaarsdam L, Guemez-Gamboa A. Genetic Causes and Modifiers of Autism Spectrum Disorder. Front Cell Neurosci. 2019 Aug 20;13:385. doi: 10.3389/fncel.2019.00385. PMID: 31481879; PMCID: PMC6710438.
  10. Courchesne E, Pramparo T, Gazestani VH, Lombardo MV, Pierce K, Lewis NE. The ASD Living Biology: from cell proliferation to clinical phenotype. Mol Psychiatry. 2019 Jan;24(1):88-107. doi: 10.1038/s41380-018-0056-y. Epub 2018 Jun 22. PMID: 29934544; PMCID: PMC6309606.
  11. Saad AK, Akour A, Mahboob A, AbuRuz S, Sadek B. Role of Brain Modulators in Neurodevelopment: Focus on Autism Spectrum Disorder and Associated Comorbidities. Pharmaceuticals (Basel). 2022 May 16;15(5):612. doi: 10.3390/ph15050612. PMID: 35631438; PMCID: PMC9144645.
  12. Isam W. Nasr, Young Chun, Sujatha Kannan, Neuroimmune responses in the developing brain following traumatic brain injury, Experimental Neurology, Volume 320, 2019, 112957, ISSN 0014-4886, https://doi.org/10.1016/j.expneurol.2019.112957.
  13. Chang HK, Hsu JW, Wu JC, Huang KL, Chang HC, Bai YM, Chen TJ, Chen MH. Traumatic Brain Injury in Early Childhood and Risk of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: A Nationwide Longitudinal Study. J Clin Psychiatry. 2018 Oct 16;79(6):17m11857. doi: 10.4088/JCP.17m11857. PMID: 30403445.
  14. Kurowski BG, Treble-Barna A, Pilipenko V, Wade SL, Yeates KO, Taylor HG, Martin LJ, Jegga AG. Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach. Front Genet. 2019 May 22;10:481. doi: 10.3389/fgene.2019.00481. PMID: 31191606; PMCID: PMC6540783.
  15. Davidovitch, M., Stein, N., Koren, G. et al. Deviations from Typical Developmental Trajectories Detectable at 9 Months of Age in Low Risk Children Later Diagnosed with Autism Spectrum Disorder. J Autism Dev Disord 48, 2854–2869 (2018). https://doi.org/10.1007/s10803-018-3549-2

Get health & wellness advice into your inbox

Your privacy is important to us. Any information you provide to us via this website may be placed by us on servers. If you do not agree to these placements, please do not provide the information.

Best Milk Alternative
[optin-monster-inline slug="yw0fgpzdy6fjeb0bbekx"]
This content is purely informational and isn’t medical guidance. It shouldn’t replace professional medical counsel. Always consult your physician regarding treatment risks and benefits. See our editorial standards for more details.

Get our health newsletter

Get daily health and wellness advice from our medical team.
Your privacy is important to us. Any information you provide to this website may be placed by us on our servers. If you do not agree do not provide the information.

Kay Taylor

Bachelors in Neuroscience - University of Dundee

Masters in Science and Health Communication – University of Dundee, Ongoing

Autism Practitioner – Scottish Autism

They have a great interest in any form of medical communications from Medical Writing to Festival Work. They are quickly obtaining experience in communications through several avenues to improve their skill foundations in writing, presenting, public engagement, and various different tools and programs.

my.klarity.health presents all health information in line with our terms and conditions. It is essential to understand that the medical information available on our platform is not intended to substitute the relationship between a patient and their physician or doctor, as well as any medical guidance they offer. Always consult with a healthcare professional before making any decisions based on the information found on our website.
Klarity is a citizen-centric health data management platform that enables citizens to securely access, control and share their own health data. Klarity Health Library aims to provide clear and evidence-based health and wellness related informative articles. 
Email:
Klarity / Managed Self Ltd
Alum House
5 Alum Chine Road
Westbourne Bournemouth BH4 8DT
VAT Number: 362 5758 74
Company Number: 10696687

Phone Number:

 +44 20 3239 9818
arrow-right