4.7 Article Proceedings Paper

Diffusion tensor fractional anisotropy of the normal-appearing seven segments of the corpus callosum in healthy adults and relapsing-remitting multiple sclerosis patients

Journal

JOURNAL OF MAGNETIC RESONANCE IMAGING
Volume 21, Issue 6, Pages 735-743

Publisher

JOHN WILEY & SONS INC
DOI: 10.1002/jmri.20296

Keywords

diffusion tensor imaging; multiple sclerosis; corpus callosum

Funding

  1. NIBIB NIH HHS [R01 EB02095] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS31499] Funding Source: Medline

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Purpose: To investigate the utility of whole-brain diffusion tensor imaging (DTI) in elucidating the pathogenesis of multiple sclerosis (MS) using the normal-appearing white matter (NAWM) of the corpus callosum (CC) as a marker of occult disease activity. Materials and Methods: A high signal-to-noise ratio (SNR) and optimized entire brain DTI data were acquired in 26 clinically-definite relapsing and,remitting multiple sclerosis (RRMS) patients and 32, age-matched healthy adult controls. The fractional anisotropy (FA) values of seven functionally distinct regions in the normal-appearing CC were compared between patients and controls. Results: This, study indicates that, 1) there was a gender-independent FA heterogeneity of, the functionally specialized CC segments in normal volunteers; 2) FA in the MS group was significantly decreased in the anterior (P = 0.0039) and posterior (P = 0.0018) midbody subdivisions of the CC, possibly due-to a reduction of small-caliber axons; and 3) the FA of the genu of the CC was relatively intact in the MS pad is compared to the healthy age-matched controls, (P = 0.644), while the splenium showed an insignificant, trend of reduced FA values (P = 0.248). The decrease in FA in any, of the CC subdivisions did not correlate with disease duration (DD) or the expanded disability status scale (EDSS) score. Conclusion: The preliminary results are consistent with published histopathology and clinical studies on MS, but not with some published DTI reports. This study provides insights into the pathogenesis of MS, and the role played by compromised axonal integrity in this disease.

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