Water and metabolite transverse T2 relaxation time abnormalities in the white matter in schizophrenia

Fei Du1, Alissa Cooper, Bruce M Cohen

  • 1McLean Hospital, Belmont, MA 02478, USA.

Schizophrenia Research
|February 24, 2012
PubMed

Insights

Schizophrenia patients show altered white matter integrity. Water T2 relaxation times were longer, while N-acetylaspartate (NAA) T2 relaxation times were shorter in patients with schizophrenia compared to healthy controls.

Area of Science:

  • Neuroimaging
  • Neuroscience
  • Biochemistry

Background:

  • White matter microstructural abnormalities are implicated in schizophrenia pathophysiology.
  • Diffusion MRI is commonly used, but transverse relaxation times (T2) offer complementary insights into molecular interactions.
  • Water and N-acetylaspartate (NAA) T2 values reflect distinct intra- and extracellular processes.

Purpose of the Study:

  • To investigate differences in water and NAA T2 relaxation times in the white matter of patients with schizophrenia (SZ) compared to healthy controls (HC).
  • To explore the relationship between T2 relaxation times and white matter microenvironment alterations in schizophrenia.

Main Methods:

  • Collected water and NAA T2 data from 16 HC and 16 SZ subjects.
  • Utilized 4 Tesla (4 T) magnetic resonance imaging (MRI).
  • Focused analysis on a 9 cm(3) voxel in the right prefrontal white matter.

Main Results:

  • The SZ group exhibited significantly longer water T2 relaxation times compared to the HC group.
  • The SZ group showed significantly shorter NAA T2 relaxation times compared to the HC group.
  • A significant metabolite × group interaction was observed (F(18,1):4.980, p=0.039).

Conclusions:

  • The observed pattern of prolonged water T2 and shortened NAA T2 suggests impoverished white matter macromolecule structures, potentially including myelin.
  • Findings indicate abnormal intra-axonal milieu and volume in the white matter of individuals with schizophrenia.
  • T2 relaxation times provide valuable information on molecular and microstructural changes in schizophrenia.