Division of Psychological Medicine, Institute of Psychiatry, Kings College London, UK
Department of Psychiatry, Eginition Hospital, University of Athens, Greece
Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, Australia
Personal Assessment and Crisis Evaluation (PACE) Clinic, Orygen Research Centre, Australia
Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, Australia
Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, and Brain Research Institute, Melbourne, Australia
Orygen Research Centre, Australia
Division of Psychological Medicine, Institute of Psychiatry, Kings College London, UK
Personal Assessment and Evaluation (PACE) Clinic, Orygen Research Centre, Australia
Department of Psychiatry, Eginition Hospital, University of Athens, Greece
Division of Psychological Medicine, Institute of Psychiatry, Kings College London, UK
Early Psychosis Prevention and Intervention Centre (EPPIC), Orygen Research Centre, Australia
Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, and Centre for Neuroscience, University of Melbourne, Australia
Correspondence: Dr Carmine M. Pariante, Division of Psychological Medicine, Box PO51, Institute of Psychiatry, Kings College London, 1 Windsor Walk, Denmark Hill, London SE5 8AF, UK. Tel: +44(0)20 7848 0807; fax: +44 (0)20 7848 0051; e-mail: spjucmp{at}iop.kcl.ac.uk
Declaration of interest None. Funding detailed in Acknowledgements.
Background Patients with psychosis have activation of the hypothalamicpituitaryadrenal (HPA) axis during the acute phase of the psychosis. Whether this has any morphological consequences for the pituitary gland is currently unknown.
Aims To examine pituitary volume variation in people at different stages of psychotic disorder.
Method Pituitary volume was measured using 1.5 mm, coronal magnetic resonance images in 24 people with first-episode psychosis, 51 with established schizophrenia and 59 healthy controls.
Results Compared with the control group, the people with first-episode psychosis had pituitary volumes that were 10% larger, whereas those with established schizophrenia had pituitary volumes that were 17% smaller. In both of the groups with psychosis, there was no difference in pituitary volume between those receiving typical antipsychotic drugs and those receiving atypical antipsychotics.
Conclusions The first episode of a psychosis is associated with a larger pituitary volume, which we suggest is due to activation of the HPA axis. The smaller pituitary volume in the group with established schizophrenia could be the consequence of repeated episodes of HPA axis hyperactivity.
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