[HTML][HTML] Characterizing the microstructural basis of “unidentified bright objects” in neurofibromatosis type 1: A combined in vivo multicomponent T2 relaxation and multi …
NeuroImage: Clinical, 2014•Elsevier
Introduction The histopathological basis of “unidentified bright objects”(UBOs)(hyperintense
regions seen on T2-weighted magnetic resonance (MR) brain scans in neurofibromatosis-1
(NF1)) remains unclear. New in vivo MRI-based techniques (multi-exponential T2 relaxation
(MET2) and diffusion MR imaging (dMRI)) provide measures relating to microstructural
change. We combined these methods and present previously unreported data on in vivo
UBO microstructure in NF1. Methods 3-Tesla dMRI data were acquired on 17 NF1 patients …
regions seen on T2-weighted magnetic resonance (MR) brain scans in neurofibromatosis-1
(NF1)) remains unclear. New in vivo MRI-based techniques (multi-exponential T2 relaxation
(MET2) and diffusion MR imaging (dMRI)) provide measures relating to microstructural
change. We combined these methods and present previously unreported data on in vivo
UBO microstructure in NF1. Methods 3-Tesla dMRI data were acquired on 17 NF1 patients …
Introduction
The histopathological basis of “unidentified bright objects” (UBOs) (hyperintense regions seen on T2-weighted magnetic resonance (MR) brain scans in neurofibromatosis-1 (NF1)) remains unclear. New in vivo MRI-based techniques (multi-exponential T2 relaxation (MET2) and diffusion MR imaging (dMRI)) provide measures relating to microstructural change. We combined these methods and present previously unreported data on in vivo UBO microstructure in NF1.
Methods
3-Tesla dMRI data were acquired on 17 NF1 patients, covering 30 white matter UBOs. Diffusion tensor, kurtosis and neurite orientation and dispersion density imaging parameters were calculated within UBO sites and in contralateral normal appearing white matter (cNAWM). Analysis of MET2 parameters was performed on 24 UBO–cNAWM pairs.
Results
No significant alterations in the myelin water fraction and intra- and extracellular (IE) water fraction were found. Mean T2 time of IE water was significantly higher in UBOs. UBOs furthermore showed increased axial, radial and mean diffusivity, and decreased fractional anisotropy, mean kurtosis and neurite density index compared to cNAWM. Neurite orientation dispersion and isotropic fluid fraction were unaltered.
Conclusion
Our results suggest that demyelination and axonal degeneration are unlikely to be present in UBOs, which appear to be mainly caused by a shift towards a higher T2-value of the intra- and extracellular water pool. This may arise from altered microstructural compartmentalization, and an increase in ‘extracellular-like’, intracellular water, possibly due to intramyelinic edema. These findings confirm the added value of combining dMRI and MET2 to characterize the microstructural basis of T2 hyperintensities in vivo.
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