Neuroanatomical correlates of different vulnerability states for psychosis and their clinical outcomes

Br J Psychiatry. 2009 Sep;195(3):218-26. doi: 10.1192/bjp.bp.108.052068.

Abstract

Background: Structural brain abnormalities have been described in individuals with an at-risk mental state for psychosis. However, the neuroanatomical underpinnings of the early and late at-risk mental state relative to clinical outcome remain unclear.

Aims: To investigate grey matter volume abnormalities in participants in a putatively early or late at-risk mental state relative to their prospective clinical outcome.

Method: Voxel-based morphometry of magnetic resonance imaging data from 20 people with a putatively early at-risk mental state (ARMS-E group) and 26 people with a late at-risk mental state (ARMS-L group) as well as from 15 participants with at-risk mental states with subsequent disease transition (ARMS-T group) and 18 participants without subsequent disease transition (ARMS-NT group) were compared with 75 healthy volunteers.

Results: Compared with healthy controls, ARMS-L participants had grey matter volume losses in frontotemporolimbic structures. Participants in the ARMS-E group showed bilateral temporolimbic alterations and subtle prefrontal abnormalities. Participants in the ARMS-T group had prefrontal alterations relative to those in the ARMS-NT group and in the healthy controls that overlapped with the findings in the ARMS-L group.

Conclusions: Brain alterations associated with the early at-risk mental state may relate to an elevated susceptibility to psychosis, whereas alterations underlying the late at-risk mental state may indicate a subsequent transition to psychosis.

Publication types

  • Multicenter Study

MeSH terms

  • Adult
  • Brain Mapping / methods
  • Case-Control Studies
  • Disease Susceptibility / pathology
  • Female
  • Humans
  • Image Interpretation, Computer-Assisted / methods
  • Magnetic Resonance Imaging / methods*
  • Male
  • Prefrontal Cortex / pathology*
  • Prognosis
  • Psychotic Disorders / pathology*
  • Risk Assessment
  • Risk Factors
  • Statistics as Topic
  • Temporal Lobe / pathology*
  • Young Adult