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Association of Brain Age With Physical Disability and Cognitive Impairment in People With Multiple Sclerosis of the Same Age.

January 27, 2026pubmed logopapers

Authors

Bos L,Wink AM,Cole JH,Strijbis EMM,Moraal B,Killestein J,Vrenken H,Uitdehaag BMJ,Barkhof F,Schoonheim MM,Jasperse B

Affiliations (2)

  • MS Center Amsterdam, Radiology and Nuclear Medicine, Neurology, Anatomy and Neurosciences, Amsterdam Neuroscience, Amsterdam UMC location VUmc, the Netherlands; and.
  • UCL London, Institutes of Neurology and Healthcare Engineering, United Kingdom.

Abstract

The brain-predicted age difference (brain-PAD) is a novel marker of neurodegeneration in multiple sclerosis (MS). Brain-PAD has been associated with clinical disability in heterogeneous MS patient cohorts of varying ages and disease durations. In this study, we investigate the relation between clinical disability and brain-PAD in a unique birth-year cohort of people with MS (pwMS) and healthy controls (HCs) of the same age all born in 1966, eliminating age as a confounding factor. This was a cross-sectional cohort study conducted in the Netherlands. Disability was quantified using the expanded disability status scale (EDSS), 9-hole peg test (9HPT), and the timed 25-foot walk test (T25FWT). Cognition was assessed using the Minimal Assessment of Cognitive Function in MS battery. The brain-PAD was calculated by subtracting the person's chronological age from the predicted brain age derived from 3-dimensional T1-weighted brain MRI scans using machine learning (brainageR software). Brain-PAD for HCs and MS subtypes (relapsing remitting, secondary progressive, and primary progressive) were compared using a generalized linear model. The relation between brain-PAD and disease duration and disability and cognitive measures were tested using univariate linear regression. In addition, the clinical explanatory value added by brain-PAD to those of brain parenchymal fraction (BPF) and T2 lesion volume was investigated. The study included 116 HC (mean age 52.9 ± 1.1 years, 61% female) and 237 pwMS (mean age 52.9 ± 0.9 years, median disease duration 16.3 years [interquartile range 8.2-24.4] and a median EDSS of 3.5 [interquartile range 2.5-4.0]). Brain-PAD was higher in pwMS compared with HC by 9.7 years (SE = 0.82, <i>p</i> < 0.0001). Longer disease duration was associated with a higher brain-PAD (β = 0.21, <i>p</i> < 0.001). A higher brain-PAD was associated with worse performance on the T25FWT (β = 0.0063, <i>p</i> < 0.05), 9HPT (β = 0.0074, <i>p</i> < 0.001), and EDSS (β = 0.028, <i>p</i> < 0.05). Brain-PAD was higher for cognitively impaired people with MS, compared with cognitively preserved pwMS and HC (<i>p</i> < 0.0001). Brain-PAD had added explanatory value over BPF in clinical outcome measures. In a cohort unbiased by age differences, greater brain ageing was associated with worse performance on disability and cognitive tests, underscoring the potential of brain-PAD as a marker for neurodegeneration and disease severity in MS.

Topics

Multiple SclerosisBrainCognitive DysfunctionAgingJournal Article

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