4.5 Article

Multimodal assessment of white matter microstructure in antipsychotic-naive schizophrenia patients and confounding effects of recreational drug use

Journal

BRAIN IMAGING AND BEHAVIOR
Volume 15, Issue 1, Pages 36-48

Publisher

SPRINGER
DOI: 10.1007/s11682-019-00230-4

Keywords

Schizophrenia; White matter; Antipsychotic-naive; Diffusion tensor imaging; Magnetization transfer; MRI

Categories

Funding

  1. Lundbeck Foundation [R25-A2701]

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The study investigated cerebral white matter integrity in antipsychotic-naive, first-episode schizophrenia patients using diffusion tensor imaging (DTI) and magnetization transfer imaging (MTI. The results suggest disorganized white matter microstructure in patients, potentially related to neuroinflammation based on higher extracellular free-water concentrations in substance-free patients. Psychopathology was not significantly associated with the observed patterns, highlighting the importance of considering recreational substance use as a confounding factor in future white matter studies.
Cerebral white matter (WM) aberrations in schizophrenia have been linked to multiple neurobiological substrates but the underlying mechanisms remain unknown. Moreover, antipsychotic treatment and substance use constitute potential confounders. Multimodal studies using diffusion tensor imaging (DTI) and magnetization transfer imaging (MTI) may provide deeper insight into the whole brain WM pathophysiology in schizophrenia. We combined DTI and MTI to investigate WM integrity in 51 antipsychotic-naive, first-episode schizophrenia patients and 55 matched healthy controls, using 3 T magnetic resonance imaging (MRI). Psychopathology was assessed with the positive and negative syndrome scale (PANSS). A whole brain partial least squares correlation (PLSC) method was used to conjointly analyze DTI-derived measures (fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity (RD), mode of anisotropy (MO)) and the magnetization transfer ratio (MTR) to identify group differences, and associations with psychopathology. In secondary analyses, we excluded recreational substance users from both groups resulting in 34 patients and 51 healthy controls. The primary PLSC group difference analysis identified a significant pattern of lower FA, AD, MO and higher RD in patients (p = 0.04). This pattern suggests disorganized WM microstructure in patients. The secondary PLSC group difference analysis without recreational substance users revealed a significant pattern of lower FA and higher AD, RD, MO, MTR in patients (p = 0.04). This pattern in the substance free patients is consistent with higher extracellular free-water concentrations, which may reflect neuroinflammation. No significant associations with psychopathology were observed. Recreational substance use appears to be a confounding issue, which calls for attention in future WM studies.

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