21 Citations (Scopus)

Abstract

Objective: Ventricular enlargement is common in established schizophrenia; however, data from ultra high-risk for psychosis and first-episode psychosis studies are inconclusive. This study aims to investigate ventricular volumes at different stages of psychosis. Methods: Ventricular volumes were measured using a semi-automated and highly reliable method, for 89 established schizophrenia, 162 first-episode psychosis, 135 ultra high-risk for psychosis and 87 healthy controls using 1.5T magnetic resonance images. Clinical outcome diagnoses for ultra high-risk for psychosis were evaluated at long-term follow-up (mean: 7.5 years). Results: Compared to controls, we identified significant ventricular enlargement of 36.2% in established schizophrenia (p < 0.001). Ventricular enlargement was not significant in first-episode psychosis (6%) or ultra high-risk for psychosis (-3%). Examination across stages of schizophrenia-spectrum diagnoses subgroups revealed a significant linear trend (p = 0.006; established schizophrenia = 36.2%, first-episode psychosis schizophrenia = 18.5%, first-episode psychosis schizophreniform = -4.2% and ultra high-risk for psychosis-schizophrenia converters = -18.5%). Conclusion: Ventricular enlargement is apparent in patients with established schizophrenia but is not a feature at the earliest stages of illness (ultra high-risk for psychosis and first-episode psychosis). Further research is needed to fully characterize the nature and timing of ventricular volume changes early in the course of illness and how these changes impact outcomes.

Original languageEnglish
JournalAustralian and New Zealand Journal of Psychiatry
Volume51
Issue number10
Pages (from-to)1041-1051
Number of pages11
ISSN0004-8674
DOIs
Publication statusPublished - 01.10.2017

Funding

This study was supported by National Health and Medical Research Council of Australia (NHMRC) Project (209062) and Program Grants (350241, 566529), and by the Colonial Foundation. G.E.B. was supported by a Young Investigator award from the Swiss National Science Foundation (University of Basel, Switzerland) and a research fellowship from the M & W Lichtenstein Foundation. C.F.B. was supported by a NHMRC Clinical Research Fellowship (567042) and a University of Melbourne Department of Psychiatry John and Betty Lynch Fellowship. A.L. was supported by a NHMRC Early Career Fellowship (1072593). S.K.W. was supported by a NHMRC Clinical Career Developmental Award (359223) and a NARSAD Young Investigator Award. B.N. was supported by a NHMRC Career Development Fellowship (1027532) and NARSAD Independent Investigator Award. A.R.Y. was supported by a NHMRC Senior Research Fellowship (566593). W.J.B. was supported by a NHMRC Career Development Fellowship (454792). P.D.M. and C.P. were each supported by NHMRC Senior Principal Research Fellowships (P.D.M.: 1060996; C.P.: 628386 and 1105825) and NARSAD Distinguished Investigator Awards.

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