Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-18T18:18:56.789Z Has data issue: false hasContentIssue false

Structural Brain Abnormalities in Early Onset Psychosis: Results from Nhe norment eop Cohort

Published online by Cambridge University Press:  23 March 2020

V. Lonning
Affiliation:
University of Oslo, Norment part Uio, oslo, Norway
S. Nerland
Affiliation:
Norment and K.G. Jebsen centre for psychosis research- institute of clinical medicine- university of Oslo, department of psychiatric research- diakonhjemmet hospital, Oslo, Norway
R.E. Smelror
Affiliation:
Norment and K.G. Jebsen centre for psychosis research- institute of clinical medicine- university of Oslo, department of psychiatric research- diakonhjemmet hospital, Oslo, Norway
T.P. Gurholt
Affiliation:
University of Oslo, Norment part Uio, oslo, Norway
I. Agartz
Affiliation:
Norment and K.G. Jebsen centre for psychosis research- institute of clinical medicine- university of Oslo, department of psychiatric research- diakonhjemmet hospital, Oslo, Norway

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.
Introduction

Cortical brain abnormalities are frequently observed in adults with psychotic disorders, but few studies have investigated adolescents with early-onset psychosis (EOP). A previous magnetic resonance imaging (MRI) study from the NORMENT group in Norway, found widespread cortical thinning and smaller subcortical volumes in adult patients with psychotic disorders, particularly schizophrenia, compared to healthy controls.

Methods

Participants from the ongoing NORMENT adolescent EOP-study, 30 patients (age: 13.3–18.3 years, mean age: 16.5, 66% female) and 45 healthy adolescents (age: 13.6–18.8 years, mean age: 16.2, 58% female), underwent 3 T MRI on the same scanner. Surface-based morphometric analyses were performed using FreeSurfer version 5.3.0. Group differences in vertex-wise cortical volume, thickness and surface area were investigated by fitting general linear models at each vertex on the surface. Age, sex and group were entered as covariates, and a non-parametric cluster-wise correction method for multiple comparisons was applied and cluster-forming and cluster-wise threshold set at 0.05.

Results

Preliminary results show thinner cortex in the left medial frontal lobe and smaller surface area in the left temporoparietal junction in EOP patients compared to healthy controls after correction for multiple comparisons.

Conclusion

Surface-based analysis is sensitive to alterations in cortical morphology in an adolescent EOP sample. The regions exhibiting reduced cortical thickness and area in EOP overlap with findings in an adult psychosis sample. Large-scale studies are warranted to better identify the pattern of abnormalities and clarify effects of age, diagnosis and medication.

Disclosure of interest

The authors have not supplied their declaration of competing interest.

Type
Workshop: brain changes in early onset psychosis
Copyright
Copyright © European Psychiatric Association 2017
Submit a response

Comments

No Comments have been published for this article.