Investigating microbleeds and white matter hyperintensities in TBI at a tract-level: A DTI study

Objectives

This study aimed to determine whether focal MRI lesions such as microbleeds (MBs) and focal white matter hyperintensities (FWMHs) serve as reliable and specific markers for tract-level white matter injury in traumatic brain injury (TBI).

Materials & methods

Twenty-two patients with moderate-to-severe TBI and 22 age-matched healthy controls underwent MRI on a 3 T Siemens Prisma scanner. Imaging included susceptibility-weighted imaging (SWI), fluid-attenuated inversion recovery (FLAIR), and diffusion tensor imaging (DTI). Focal lesions were manually identified on SWI and FLAIR and mapped onto tractography reconstructions. Diffusion metrics—fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) were compared between lesion-affected tracts, contralateral normal-appearing white matter (NAWM), and corresponding control tracts. Statistical analyses were performed using repeated measures ANOVA with Greenhouse-Geisser correction and Bonferroni-adjusted post hoc tests for FA. Friedman tests were conducted for MD, AD, and RD, followed by Bonferroni-corrected Wilcoxon post hoc comparisons.

Results

In this study, we identified 27 MBs and 66 FWMHs intersecting white matter tracts. We observed notable differences in diffusion metrics when comparing lesion-affected tracts to healthy controls. In MB-affected tracts, fractional anisotropy (FA) differed significantly (p = 0.002), while mean diffusivity (MD) also showed a significant alteration (p = 0.002), along with radial diffusivity (RD) (p < 0.001). Similarly, in FWMH-affected tracts, significant differences were observed in FA (p < 0.001), MD (p < 0.001), axial diffusivity (AD) (p < 0.001), and RD (p < 0.001). However, we did not find any significant differences between lesion-affected tracts and the contralateral normal-appearing white matter (NAWM).

Conclusion

MBs and FWMHs do not co-localize with axonal injury at the tract level but indicate a global white matter damage.