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Microstructural characterization of multiple sclerosis lesion phenotypes using multiparametric longitudinal analysis

  • Veronica Ravano,
  • Michaela Andelova,
  • Gian Franco Piredda,
  • Stefan Sommer,
  • Samuele Caneschi,
  • Lucia Roccaro,
  • Jan Krasensky,
  • Matej Kudrna,
  • Tomas Uher,
  • Ricardo A. Corredor-Jerez,
  • Jonathan A. Disselhorst,
  • Bénédicte Maréchal,
  • Tom Hilbert,
  • Jean-Philippe Thiran,
  • Jonas Richiardi,
  • Dana Horakova,
  • Manuela Vaneckova,
  • Tobias Kober

摘要

Background and objectives

In multiple sclerosis (MS), slowly expanding lesions were shown to be associated with worse disability and prognosis. Their timely detection from cross-sectional data at early disease stages could be clinically relevant to inform treatment planning. Here, we propose to use multiparametric, quantitative MRI to allow a better cross-sectional characterization of lesions with different longitudinal phenotypes.

Methods

We analysed T1 and T2 relaxometry maps from a longitudinal cohort of MS patients. Lesions were classified as enlarging, shrinking, new or stable based on their longitudinal volumetric change using a newly developed automated technique. Voxelwise deviations were computed as z-scores by comparing individual patient data to T1, T2 and T2/T1 normative values from healthy subjects. We studied the distribution of microstructural properties inside lesions and within perilesional tissue.

Results and conclusions

Stable lesions exhibited the highest T1 and T2 z-scores in lesion tissue, while the lowest values were observed for new lesions. Shrinking lesions presented the highest T1 z-scores in the first perilesional ring while enlarging lesions showed the highest T2 z-scores in the same region. Finally, a classification model was trained to predict the longitudinal lesion type based on microstructural metrics and feature importance was assessed. Z-scores estimated in lesion and perilesional tissue from T1, T2 and T2/T1 quantitative maps carry discriminative and complementary information to classify longitudinal lesion phenotypes, hence suggesting that multiparametric MRI approaches are essential for a better understanding of the pathophysiological mechanisms underlying disease activity in MS lesions.