Longitudinal Gray Matter Development Associated With Psychotic Experiences in Young People

• Published in: Biological psychiatry global open science Vol. 3; no. 2; pp. 264 - 273
• Main Authors: O'Neill, Aisling, Dooley, Niamh, Healy, Colm, Carey, Eleanor, Roddy, Darren, Frodl, Thomas, O’Hanlon, Erik, Cannon, Mary
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.04.2023; Elsevier
• Subjects: Adolescence; Archival Report; Gray matter; Longitudinal; Psychosis; Psychotic experiences; Structural imaging; Psychosis; Adolescence; Longitudinal; Gray matter; Structural imaging; Psychotic experiences
• ISSN: 2667-1743; 2667-1743
• DOI: 10.1016/j.bpsgos.2022.02.003

Gray matter abnormalities are observed across the psychosis spectrum. The trajectory of these abnormalities in healthy adolescents reporting subthreshold psychotic experiences (PEs) may provide insight into the neural mechanisms underlying psychotic symptoms. The risk of psychosis and additional psychopathology is even higher among these individuals who also report childhood adversity/DSM-5 diagnoses. Thus, the aims of this longitudinal study were to investigate PE-related volumetric changes in young people, noting any effects of childhood adversity/DSM-5 diagnosis. A total of 211 young people 11 to 13 years of age participated in the initial Adolescent Brain Development study. PE classification was determined by expert consensus at each time point. Participants underwent neuroimaging at 3 time points over 6 years. A total of 76 participants with at least one scan were included in the final sample; 34 who met criteria for PEs at least once across all the time points (PE group) and 42 control subjects. Data from 20 bilateral regions of interest were extracted for linear mixed-effects analyses. Right hippocampal volume increased over time in the control group, with no increase in the PE group (p = .00352). DSM-5 diagnosis and childhood adversity were not significantly associated with right hippocampal volume. There was no significant effect of group or interaction in any other region. These findings further implicate right hippocampal volumetric abnormalities in the pathophysiology underlying PEs. Furthermore, as suggested by previous studies in those at clinical high risk for psychosis and those with first-episode psychosis, it is possible that these deficits may be a marker for later clinical outcomes.