Journal
ANNALS OF NEUROLOGY
Volume 87, Issue 5, Pages 725-738Publisher
WILEY
DOI: 10.1002/ana.25706
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Funding
- Vidi Grant of the Dutch Research Council (Netherlands Organization for Scientific Research) [VIDI-452-16-015]
- ALWopen grant [ALWOP.179]
- MQ Fellowship
- Netherlands Organization for Scientific Research Vici Grant
- ALS Foundation Netherlands
- Weston Brain Institute Rapid Response grant
- Health Research Board (HRB-Ireland) [HRB EIA-2017-019]
- Research Motor Neuron Foundation
- Irish Motor Neuron Disease Association
- Health Research Board and Science Foundation Ireland
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Objective: Clinical trials in amyotrophic lateral sclerosis (ALS) continue to rely on survival or functional scales as end-points, despite the emergence of quantitative biomarkers. Neuroimaging-based biomarkers in ALS have been shown to detect ALS-associated pathology in vivo, although anatomical patterns of disease spread are poorly characterized. The objective of this study is to simulate disease propagation using network analyses of cerebral magnetic resonance imaging (MRI) data to predict disease progression. Methods: Using brain networks of ALS patients (n = 208) and matched controls across longitudinal time points, network-based statistics unraveled progressive network degeneration originating from the motor cortex and expanding in a spatiotemporal manner. We applied a computational model to the MRI scan of patients to simulate this progressive network degeneration. Simulated aggregation levels at the group and individual level were validated with empirical impairment observed at later time points of white matter and clinical decline using both internal and external datasets. Results: We observe that computer-simulated aggregation levels mimic true disease patterns in ALS patients. Simulated patterns of involvement across cortical areas show significant overlap with the patterns of empirically impaired brain regions on later scans, at both group and individual levels. These findings are validated using an external longitudinal dataset of 30 patients. Interpretation: Our results are in accordance with established pathological staging systems and may have implications for patient stratification in future clinical trials. Our results demonstrate the utility of computational models in ALS to predict disease progression and underscore their potential as a prognostic biomarker.
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