4.5 Article

Pituitary volume in unaffected relatives of patients with schizophrenia and bipolar disorder

Journal

PSYCHONEUROENDOCRINOLOGY
Volume 33, Issue 7, Pages 1004-1012

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.psyneuen.2008.05.010

Keywords

pituitary; schizophrenia; bipolar disorder; hypothatamic-pituitary-adrenal (HPA) axis; psychosis; relatives

Funding

  1. King's College Development Trust (UK)
  2. NARSAD Mental Health Research Association
  3. UK Medical Research Council (MRC)
  4. American Psychiatric Institute for Research and Education (APIRE)
  5. British Academy, the Guy's and St. Thomas' Charitable Trust
  6. NIHR Biomedical Research Centre for Mental Health at the South London
  7. Maudstey NHS Foundation Trust & The Institute of Psychiatry, Kings' College London
  8. Wellcome Trust
  9. Stanley Foundation
  10. MRC [G108/603] Funding Source: UKRI
  11. Medical Research Council [G108/603] Funding Source: researchfish

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Background: Hypothalamic-pituitary-adrenal (HPA) axis hyperactivity has been demonstrated in both schizophrenia and bipolar disorder, but the mechanisms underlying this abnormality are still unclear. Enlarged pituitary volume has been recently reported in patients with first episode psychosis and been interpreted as a consequence of an increased activation of the HPA axis. The aim of this study was to assess the contribution of familial liability to pituitary volume in schizophrenia and bipolar disorder. Pituitary volume may be an indirect measure of HPA axis activity. Methods: MRI brain scans and measurements of pituitary volumes were obtained for 183 subjects: 26 patients with established schizophrenia or schizoaffective disorder, 44 of their unaffected first-degree relatives (22 familial schizophrenia, 22 non-familial schizophrenia), 29 patients with established bipolar disorder, 38 of their unaffected first-degree relatives, and 46 healthy comparison subjects. Results: We found a significantly Larger pituitary volume (effect size = 0.7) in unaffected relatives of patients with schizophrenia compared with controls (p = 0.002); the pituitary was even Larger in relatives of patients with familial schizophrenia (effect size = 0.8, p = 0.005). We did not find a significant difference in pituitary volume when comparing the relatives of bipolar patients with controls. Among patients, those with schizophrenia who were receiving prolactin-elevating anti-psychotics had an increased pituitary volume compared with controls (effect size = 1.0, p = 0.006). Conclusions: These results suggest that the larger pituitary volume previously reported in first episode schizophrenia could be partly due to a genetic susceptibility to over-activate the HPA axis. (c) 2008 Elsevier Ltd. All rights reserved.

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