4.7 Article

Brain free water alterations in first-episode psychosis: a longitudinal analysis of diagnosis, course of illness, and medication effects

Journal

PSYCHOLOGICAL MEDICINE
Volume 51, Issue 6, Pages 1001-1010

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291719003969

Keywords

DTI; first episode psychosis; FW; putative neuroinflammatory biomarker

Funding

  1. National Institute of Health [R01MH105411, 5R01MH059883]
  2. Building Interdisciplinary Research Careers in Women's Health award [K12 HD051958]
  3. National Institute of Child Health and Human Development (NICHD), Office of Research on Women's Health, Office of Dietary Supplements
  4. National Institute of Aging
  5. [R01MH 084895]

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The study found that patients with schizophrenia and bipolar disorder with psychotic features exhibit increased free water (FW) at illness onset, which remains stable during the early course of the illness with no evidence of progression or remission. Preliminary analyses suggest that antipsychotic medication exposure may be associated with higher FW in gray matter in patients with bipolar disorder. Higher FW in white matter correlates with the severity of negative symptoms.
Background Multiple lines of evidence suggest the presence of altered neuroimmune processes in patients with schizophrenia (Sz) and severe mood disorders. Recent studies using a novel free water diffusion tensor imaging (FW DTI) approach, proposed as a putative biomarker of neuroinflammation, atrophy, or edema, have shown significantly increased FW in patients with Sz. However no studies to date have investigated the longitudinal stability of FW alterations during the early course of psychosis, nor have studies focused separately on FE psychosis patients with Sz or bipolar disorder (BD) with psychotic features. Methods The current study included 188 participants who underwent diffusion magnetic resonance imaging scanning at baseline. Sixty-four participants underwent follow-up rescanning after 12 months. DTI-based alterations in patients were calculated using voxelwise tract-based spatial statistics and region of interest analyses. Results Patients with FE psychosis, both Sz and BD, exhibited increased FW at illness onset which remained unchanged over the 12-month follow-up period. Preliminary analyses suggested that antipsychotic medication exposure was associated with higher FW in gray matter that reached significance in the BD group. Higher FW in white matter correlated with negative symptom severity. Conclusions Our results support the presence of elevated FW at the onset of psychosis in both Sz and BD, which remains stable during the early course of the illness, with no evidence of either progression or remission.

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