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Pain Modulation Mechanisms in ASD Adults
A Dubois1,2,3, M Boudjarane4, A Le Fur-Bonnabesse4
1LP3C - EA1285, Department of Psychology, University of Western Brittany, Brest, France. amandine.dubois@univ-brest.fr.
Journal of Autism and Developmental Disorders
|February 11, 2020
Summary
Adults with autism spectrum disorder (ASD) show similar pain modulation to neurotypical individuals. However, pain scores in the ASD group were highly variable, indicating a need for careful interpretation of results.
Area of Science:
- Neuroscience
- Psychology
- Autism Spectrum Disorders Research
Background:
- Understanding endogenous pain modulation is crucial for pain management.
- Autism Spectrum Disorders (ASD) may involve atypical sensory processing, including pain perception.
- Previous research has shown varied results regarding pain modulation in ASD.
Purpose of the Study:
- To investigate endogenous pain modulation mechanisms in adults with Autism Spectrum Disorders (ASD).
- To compare pain processing in adults with ASD to neurotypical controls.
- To identify potential differences in excitatory and inhibitory pain mechanisms.
Main Methods:
- Recruited 19 adults with ASD (without intellectual disabilities) and 19 matched neurotypical controls.
- Utilized an experimental pain model to assess pain modulation.
- Measured both excitatory and inhibitory pain mechanisms within a single session.
Main Results:
- No significant differences were found in endogenous pain modulation mechanisms between the ASD and control groups.
- Pain scores exhibited greater variability and a wider range of extreme scores in the ASD group compared to controls.
- No systematic dysfunction in endogenous excitatory pain modulation was observed in ASD, unlike in schizophrenia.
Conclusions:
- Endogenous pain modulation appears largely intact in adults with ASD.
- The high variability in pain scores within the ASD group necessitates cautious interpretation of findings.
- Further research is needed to understand the implications of heightened pain score variability in ASD.
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