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[The activity of complement system in children with autistic spectrum disorders]
E G Cheremnykh1, N S Karpova1, M I Factor1
1Mental Health Research Centre, Moscow, Russia.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|February 1, 2017
Summary
Complement system (CS) activity was evaluated in children with autistic spectrum disorders (ASD) and schizophrenia using a novel method. CS activity was significantly different in patients compared to controls, and lower in ASD than in schizophrenia.
Area of Science:
- Immunology
- Neuroscience
- Pediatrics
Background:
- The complement system (CS) plays a crucial role in immune responses.
- Dysregulation of the CS has been implicated in various neurological and psychiatric disorders.
- Understanding CS activity in pediatric conditions like autism spectrum disorder (ASD) and schizophrenia is essential.
Purpose of the Study:
- To develop and implement a new method for assessing complement system (CS) activity.
- To evaluate CS activity in children diagnosed with autistic spectrum disorders (ASD) and schizophrenia.
- To compare CS activity levels between these patient groups and healthy controls.
Main Methods:
- A novel method was developed to determine integral CS activity (T50) using the ciliata Tetrahymena pyriformis.
- The study included 249 patients (aged 3-14 years) with ASD or schizophrenia and 279 age-matched healthy children.
- CS activity was measured by the time of death of 50% of ciliata in a 5% blood serum concentration.
Main Results:
- Significant differences in median T50 values were observed between patient groups and controls (p<0.005).
- Patients were categorized into three groups based on CS activity: below, above, and within the control range.
- Lower CS activity was found in children with ASD compared to children with schizophrenia (p<0.005).
Conclusions:
- The developed method provides a reliable assessment of integral CS activity.
- Altered CS activity is evident in children with ASD and schizophrenia.
- CS activity is lower in children with ASD than in those with schizophrenia, suggesting distinct immune profiles.
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