| Autor: |
Conti A; Department of Biomedicine and Prevention, University of Rome 'Tor Vergata', Via Montpellier 1, 00133 Rome, Italy., Treaba CA; Massachusetts General Hospital, Boston, MA 02114, USA.; A. A. Martinos Center for Biomedical Imaging, Boston, MA 02129, USA., Mehndiratta A; Massachusetts General Hospital, Boston, MA 02114, USA.; A. A. Martinos Center for Biomedical Imaging, Boston, MA 02129, USA., Barletta VT; Massachusetts General Hospital, Boston, MA 02114, USA.; A. A. Martinos Center for Biomedical Imaging, Boston, MA 02129, USA., Mainero C; Massachusetts General Hospital, Boston, MA 02114, USA.; A. A. Martinos Center for Biomedical Imaging, Boston, MA 02129, USA., Toschi N; Department of Biomedicine and Prevention, University of Rome 'Tor Vergata', Via Montpellier 1, 00133 Rome, Italy.; Massachusetts General Hospital, Boston, MA 02114, USA.; A. A. Martinos Center for Biomedical Imaging, Boston, MA 02129, USA. |
| Abstrakt: |
To date, the relationship between central hallmarks of multiple sclerosis (MS), such as white matter (WM)/cortical demyelinated lesions and cortical gray matter atrophy, remains unclear. We investigated the interplay between cortical atrophy and individual lesion-type patterns that have recently emerged as new radiological markers of MS disease progression. We employed a machine learning model to predict mean cortical thinning in whole-brain and single hemispheres in 150 cortical regions using demographic and lesion-related characteristics, evaluated via an ultrahigh field (7 Tesla) MRI. We found that (i) volume and rimless (i.e., without a "rim" of iron-laden immune cells) WM lesions, patient age, and volume of intracortical lesions have the most predictive power; (ii) WM lesions are more important for prediction when their load is small, while cortical lesion load becomes more important as it increases; (iii) WM lesions play a greater role in the progression of atrophy during the latest stages of the disease. Our results highlight the intricacy of MS pathology across the whole brain. In turn, this calls for multivariate statistical analyses and mechanistic modeling techniques to understand the etiopathogenesis of lesions. |
