Background and ObjectivesIn multiple sclerosis (MS), neurodegeneration results from the interplay between disease-specific pathology and normal aging. Conventional MRI captures morphologic changes in neurodegeneration, while quantitative MRI (qMRI) provides biophysical measures of microstructural alterations. Combining these modalities may reveal how aging and pathology interact and contribute to disability progression in people with MS.MethodsWe analyzed cross-sectional and longitudinal morphometry data from 1,353 patients with MS and 3,462 healthy controls (HCs). In addition, cross-sectional qMRI data, available for 378 HCs and 169 patients with MS, were analyzed separately. Morphometric measures and quantitative metrics were used to estimate brain-predicted age differences (brain-PADs) with machine learning. We assessed the added value of quantitative metrics over a model based exclusively on morphometric measures in brain age prediction. We also investigated the associations of brain-PADs derived from conventional and qMRI-based predictive models with clinical disability, serum inflammatory biomarkers of neuroaxonal and astrocytic injury, and lesion burden.ResultsModels combining morphometry and qMRI data achieved the best performance (mean absolute error: 5.73), outperforming those based on qMRI (6.62) or morphometry alone (8.00). Cross-sectional and longitudinal morphometry-based brain-PAD correlated with clinical disability, serum neurofilament light chain, and serum glial fibrillary acidic protein levels (all p < 0.01), with significant longitudinal interactions with time (all p < 0.05). Cross-sectional qMRI-based brain-PAD correlated with white matter lesion count (p = 0.042, R2 = 0.028) and paramagnetic rim lesion volume (p = 0.028, R2 = 0.020).DiscussionIntegrating qMRI improves brain age predictions. Brain-PAD serves as an imaging biomarker to quantify MS-associated aging and track disability and neuroinflammation progression.
Unraveling Microstructural and Macrostructural Brain Age Dynamics in Multiple Sclerosis
Pravata, Emanuele;
2025-01-01
Abstract
Background and ObjectivesIn multiple sclerosis (MS), neurodegeneration results from the interplay between disease-specific pathology and normal aging. Conventional MRI captures morphologic changes in neurodegeneration, while quantitative MRI (qMRI) provides biophysical measures of microstructural alterations. Combining these modalities may reveal how aging and pathology interact and contribute to disability progression in people with MS.MethodsWe analyzed cross-sectional and longitudinal morphometry data from 1,353 patients with MS and 3,462 healthy controls (HCs). In addition, cross-sectional qMRI data, available for 378 HCs and 169 patients with MS, were analyzed separately. Morphometric measures and quantitative metrics were used to estimate brain-predicted age differences (brain-PADs) with machine learning. We assessed the added value of quantitative metrics over a model based exclusively on morphometric measures in brain age prediction. We also investigated the associations of brain-PADs derived from conventional and qMRI-based predictive models with clinical disability, serum inflammatory biomarkers of neuroaxonal and astrocytic injury, and lesion burden.ResultsModels combining morphometry and qMRI data achieved the best performance (mean absolute error: 5.73), outperforming those based on qMRI (6.62) or morphometry alone (8.00). Cross-sectional and longitudinal morphometry-based brain-PAD correlated with clinical disability, serum neurofilament light chain, and serum glial fibrillary acidic protein levels (all p < 0.01), with significant longitudinal interactions with time (all p < 0.05). Cross-sectional qMRI-based brain-PAD correlated with white matter lesion count (p = 0.042, R2 = 0.028) and paramagnetic rim lesion volume (p = 0.028, R2 = 0.020).DiscussionIntegrating qMRI improves brain age predictions. Brain-PAD serves as an imaging biomarker to quantify MS-associated aging and track disability and neuroinflammation progression.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
