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Updated: Jun 27, 2026

Testing Sensory and Multisensory Function in Children with Autism Spectrum Disorder
Published on: April 22, 2015
Autism-like features in individuals at clinical high risk for psychosis: a longitudinal research using the PANSS
Lorenzo Pelizza1, Teresa Flavia Picone1, Emanuela Leuci2
1Department of Biomedical and Neuromotor Sciences, Alma Mater Studiorum Università di Bologna, Bologna (BO), Italy.
Purpose:
The PANSS Autism Severity Score (PAUSS) is a widely used measure of autism-like features in early psychosis, including mental states at "Clinical High Risk for Psychosis" (CHR-P). However, evidence regarding its relevance to long-term outcomes and treatment response is very scarce. Thus, the main aim of this investigation was to compare baseline clinical characteristics and longitudinal outcomes/treatment response between CHR-P subjects with or without autistic features recruited into a specialist early intervention service during a 2-year follow-up period.
Methods:
CHR-P participants completed the Social and Occupational Functioning Assessment Scale (SOFAS) and the Positive And Negative Syndrome Scale (PANSS) at baseline and over the follow-up. Kaplan-Meyer survival analysis, mixed-design ANOVA, and binary logistic regression analysis were performed.
Results:
Thirty-six (16.8%) of the 214 enrolled CHR-P individuals scored above the PAUSS cut-off of 30 (PAUSS + subgroup). At baseline, they showed higher PANSS and SOFAS scores, as well as higher prevalence rates of substance abuse and individuals not engaged in education, employment, or training. Over the follow-up period, they showed worse clinical and functional outcomes, including higher incidence rates of hospital re-admission (28.7% vs. 11.6%; Hazard Ratio [HR] = 3.38) and conversion to psychosis (26.0% vs. 12.0%; HR = 2.71), as well as lower likelihood of both functional (Hazard Risk [HR] = 4.23) and symptomatic (HR = 6.50) remission. However, our specialist intervention has proven effective in improving psychopathological and functional parameters over time even in the PAUSS + subgroup.
Conclusions:
Our findings suggest that the PAUSS specifically identifies a CHR-P subgroup with greater clinical and functional severity at presentation and worse longitudinal outcomes.
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