Neurotensin is increased in serum of young children with autistic disorder

Asimenia Angelidou1, Konstantinos Francis, Magdalini Vasiadi

  • 1Laboratory of Molecular Immunopharmacology and Drug Discovery, Department of Pharmacology & Experimental Therapeutics, Tufts University School of Medicine, Boston, MA, USA.

Insights

Children with autism spectrum disorder (ASD) show elevated neurotensin (NT) levels, a neuropeptide linked to mast cell activation and potential brain inflammation. This finding may offer new insights into ASD

Area of Science:

  • Neuroscience
  • Immunology
  • Developmental Pediatrics

Background:

  • Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by social interaction and communication deficits, alongside repetitive behaviors.
  • Current understanding lacks definitive causes or diagnostic markers for ASD.
  • Some children with ASD exhibit allergy-like symptoms, suggesting non-allergic mast cell activation.

Purpose of the Study:

  • To investigate serum levels of neuropeptides (neurotensin, β-endorphin, substance P) in young children with autism spectrum disorder (ASD).
  • To explore the potential role of these neuropeptides in mast cell activation and neuroinflammation associated with ASD.

Main Methods:

  • Serum samples were collected from 19 children diagnosed with autistic disorder and 16 healthy controls.
  • Neuropeptide levels were quantified using Milliplex arrays.
  • Statistical analysis was performed to compare levels between groups.

Main Results:

  • Serum neurotensin (NT) levels were significantly higher in children with ASD (105.6 ± 12.4 pg/ml) compared to controls (60.5 ± 6.0 pg/ml), p = 0.004.
  • No significant differences were observed in serum levels of β-endorphin or substance P.
  • Elevated NT suggests a potential link to mast cell stimulation and neuroinflammation in ASD.

Conclusions:

  • Neurotensin (NT) is significantly elevated in young children with autism spectrum disorder (ASD).
  • This elevation suggests NT may play a role in mast cell activation and/or direct brain inflammation contributing to ASD.
  • Further research is warranted to explore NT's specific mechanisms in ASD pathogenesis.

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