[A neuroprotective approach to optimizing treatment and correction activities in children with autism spectrum

L A Tsukurova1

  • 1Research Institute of Children's Balneology, Physiotherapy and Medical Rehabilitation, Yevpatoria, Russia.

Insights

Children with autism spectrum disorder (ASD) show reduced levels of neurotrophic factors like nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF), along with heat shock proteins (Hsp27, Hsp70). This suggests impaired neuroprotection in the brain.

Area of Science:

  • Neuroscience
  • Developmental Pediatrics
  • Genetics

Background:

  • Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition.
  • Neurotrophic factors and heat shock proteins play crucial roles in neuronal development and protection.
  • Alterations in these factors may contribute to the pathophysiology of ASD.

Purpose of the Study:

  • To investigate the neuroprotective potential of heat shock proteins (Hsp) and neurotrophins in children diagnosed with ASD.
  • To quantify levels of specific neurotrophic factors and heat shock proteins in children with ASD.

Main Methods:

  • A cohort of sixty-eight children diagnosed with ASD (ICD-10 F84), aged 5–12 years, were enrolled.
  • Standard clinical examinations were conducted.
  • Blood serum levels of brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), heat shock protein 27 (Hsp27), and heat shock protein 70 (Hsp70) were measured.

Main Results:

  • A significant decrease in serum levels of NGF, BDNF, Hsp27, and Hsp70 was observed in the total group of children with ASD.
  • Boys with severe ASD exhibited particularly diminished levels of these neuroprotective factors.
  • These findings indicate a potential deficit in neuroprotective mechanisms within the brain.

Conclusions:

  • The reduced levels of NGF, BDNF, Hsp27, and Hsp70 in children with ASD suggest compromised neuroprotection.
  • These biochemical alterations highlight the need for further investigation into the underlying mechanisms of ASD.
  • Developing targeted treatment strategies to enhance neuroprotection in ASD is warranted.
Abstract

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