Hostname: page-component-7bb8b95d7b-dvmhs Total loading time: 0 Render date: 2024-09-20T15:54:19.554Z Has data issue: false hasContentIssue false

Ultra High Risk Status and Transition to Psychosis in 22q11.2 Deletion Syndrome

Published online by Cambridge University Press:  23 March 2020

M. Armando
Affiliation:
Ospedale Pediatrico Bambino Gesu, Neuroscience, Roma, Italy
M. Schneider
Affiliation:
Center for Contextual Psychiatry, Neuroscience, Leuven, Belgium
M. Pontillo
Affiliation:
Ospedale Pediatrico Bambino Gesu, Neuroscience, Roma, Italy
S. Vicari
Affiliation:
Ospedale Pediatrico Bambino Gesu, Neuroscience, Roma, Italy
M. Debbane
Affiliation:
Developmental Imaging and Psychopathology Lab, Geneva, Switzerland
F. Schultze-Lutter
Affiliation:
University hospital of child and adolescence psychiatry and psychotherapy, University hospital of child and adolescence psychiatry and psychotherapy, Bern, Switzerland
S. Eliez
Affiliation:
Department of Genetic Medicine and Development, School of Medicine, Department of Genetic Medicine and Development School of Medicine, Geneva, Switzerland

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The 22q11.2 deletion syndrome (22q11DS) is characterized by high rates of psychotic symptoms and schizophrenia, making this condition a promising human model for studying risk factors for psychosis. We explored the predictive value of ultra high-risk (UHR) criteria in a sample of patients with 22q11DS. We also examined the additional contribution of sociodemographic, clinical and cognitive variables to predict transition to psychosis within a mean interval of 32.56176 months after initial assessment. Eighty-nine participants with 22q11DS (age range: 8–30 years; mean: 16.1647) were assessed using the structured interview for psychosis-risk syndromes. Information on axis I diagnoses, internalizing and externalizing symptoms, level of functioning and IQ was also collected. At baseline, 22 (24.7%) participants met UHR criteria. Compared to those without a UHR condition, they had a significantly lower functioning, more frequent anxiety disorders and more severe psychopathology. Transition rate to psychosis was 27.3% in UHR and 4.5% in non-UHR participants. Cox regression analyses revealed that UHR status significantly predicted conversion to psychosis. Baseline level of functioning was the only other additional predictor. This is the first study investigating the predictive value of UHR criteria in 22q11DS. It indicates that the clinical path leading to psychosis is broadly comparable to that observed in other clinical high-risk samples. Nevertheless, the relatively high transition rate in non-UHR individuals suggests that other risk markers should be explored in this population. The role of low functioning as a predictor of transition to psychosis should also be investigated more in depth.

Disclosure of interest

The authors have not supplied their declaration of competing interest.

Type
Oral communications: Classification of mental disorders; comorbidity/dual pathologies; psychopathology; psychopharmacology and pharmacoeconomics and sleep disorders & stress
Copyright
Copyright © European Psychiatric Association 2017
Submit a response

Comments

No Comments have been published for this article.