High b-value diffusion-weighted imaging in progressive multifocal leukoencephalopathy in HIV patients

Claudia Godi1,2,3, Enrico De Vita2,3, Enrico Tombetti4

  • 1Neuroradiology Department, San Raffaele Scientific Institute, Milan, Italy.

European Radiology
|February 8, 2017
PubMed
Abstract

Insights

Higher b-value diffusion-weighted imaging (DWI) at 3,000 s/mm² (b3000) improves visualization of progressive multifocal leukoencephalopathy (PML) lesions. This advanced technique may offer more accurate biomarkers for PML activity and prognosis.

Area of Science:

  • Neuroimaging
  • Radiology
  • Diffusion-Weighted Imaging

Background:

  • Progressive multifocal leukoencephalopathy (PML) diagnosis relies on characteristic diffusion-weighted imaging (DWI) findings.
  • The typical DWI pattern includes an ill-defined hyperintense rim and hypointense core.
  • Optimizing DWI parameters can enhance lesion visualization and characterization.

Purpose of the Study:

  • To evaluate if a higher b-value (b3000) improves the visualization of PML lesions compared to a standard b-value (b1000).
  • To determine if b3000 provides different structural information about PML lesions.
  • To assess the impact of b3000 on the apparent diffusion coefficient (ADC) values and lesion component volumes.

Main Methods:

  • Retrospective analysis of HIV-positive patients with confirmed PML.
  • Inclusion of both b1000 and b3000 DWI sequences in the study protocol.
  • Measurement and comparison of signal intensities, ADC values, and volumes of lesion rims, cores, and normal-appearing white matter (NAWM) between b1000 and b3000.

Main Results:

  • The b3000 DWI sequence enhanced the visualization of the PML lesion rim and core.
  • Higher signal intensity was observed in the rim and lower signal intensity in the core at b3000 compared to NAWM.
  • While total lesion volumes were similar, b3000 revealed significantly larger core volumes and smaller rim volumes than b1000.
  • The hyperintense rim showed non-restricted ADCs but contained foci of restricted diffusion on both b-values.

Conclusions:

  • The b3000 DWI sequence improves contrast resolution and visualization of the characteristic rim-and-core pattern in PML.
  • b3000 reclassifies some rim tissue into the core, potentially offering more precise biomarkers for PML activity and prognosis.
  • This higher b-value DWI may lead to more accurate assessments of disease activity and tissue damage in PML.