The contribution of first-episode illness characteristics and cumulative antipsychotic usage to progressive structural brain changes over a long-term follow-up in schizophrenia

Exposure to antipsychotics as well as certain first-episode illness characteristics have been associated with greater gray matter (GM) deficits in the early phase of schizophrenia. Whether the first-episode illness characteristics affect the long-term progression of the structural brain changes rema...

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Bibliographic Details
Published in:Psychiatry Research: Neuroimaging
Main Authors: Konttajärvi, Tuomas, Haapea, Marianne, Huhtaniska, Sanna, Björnholm, Lassi, Miettunen, Jouko, Isohanni, Matti, Penttilä, Matti, Murray, Graham K., Koponen, Hannu, Vernon, Anthony C., Jääskeläinen, Erika, Lieslehto, Johannes
Format: Article in Journal/Newspaper
Language:English
Published: 2024
Subjects:
Northern Finland
Online Access:https://kclpure.kcl.ac.uk/portal/en/publications/9ffa4454-2a6b-42de-b53a-1d468c353012
https://doi.org/10.1016/j.pscychresns.2024.111790
http://www.scopus.com/inward/record.url?scp=85185556289&partnerID=8YFLogxK
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Summary:Exposure to antipsychotics as well as certain first-episode illness characteristics have been associated with greater gray matter (GM) deficits in the early phase of schizophrenia. Whether the first-episode illness characteristics affect the long-term progression of the structural brain changes remain unexplored. We therefore assessed the role of first-episode illness characteristics and life-time antipsychotic use in relation to long-term structural brain GM changes in schizophrenia. Individuals with schizophrenia (SZ, n = 29) and non-psychotic controls (n = 61) from the Northern Finland Birth Cohort 1966 underwent structural MRI at the ages of 34 (baseline) and 43 (follow-up) years. At follow-up, the average duration of illness was 19.8 years. Voxel-based morphometry was used to assess the effects of predictors on longitudinal GM changes in schizophrenia-relevant brain areas. Younger age of onset (AoO), higher cumulative antipsychotic dose and severity of symptoms were associated with greater GM deficits in the SZ group at follow-up. None of the first-episode illness characteristics were associated with longitudinal GM changes during 9-year follow-up period. We conclude that a younger AoO and high life-time antipsychotic use may contribute to progression of structural brain changes in schizophrenia. Apart from AoO, other first-episode illness characteristics may not contribute to longitudinal GM changes in midlife.

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