Accelerated frontal grey matter atrophy in relapsing remitting multiple sclerosis
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Background
Grey matter (GM) atrophy has been suggested as the most accurate marker of neurodegeneration in multiple sclerosis (MS) progression. At the same time, few studies have examined regional atrophy longitudinally and how it correlates to different clinical domains.
Methods
We used two relapsing remitting MS (RRMS) cohorts (N=250, T 1 w-scans=940) sampled for up to 12 years to map grey matter atrophy localisation, compare the examined patterns with six age-matched healthy control (HC) cohorts (N=31,427, T 1 w-scans=32,793), and associate the observed atrophy pattern with disability, cognitive decline and fatigue, measured with the Expanded Disability Status Scale (EDSS), Paced Auditory Serial Addition Test (PASAT), and Fatigue Severity Scale (FSS).
Results
The strongest, replicable significant brain atrophy patterns in RRMS were found in the frontal lobes, specifically, in the superior frontal cortices (β age ≤-0.27), pars orbitalis (β age ≤-0.25), and thalami (β age ≤-0.20). Across samples, such atrophy patterns were more pronounced than in a sample of more 20-year older HCs in the right superior frontal cortex (Z>2.41, p<0.009), right caudal middle frontal cortex (Z>2.08, p<0.019), right caudate (Z>2.09, p<0.019), and the left frontal pole (Z>2.42, p<0.008). The replicability of associations between volumetrics and clinical outcomes was limited to EDSS and the left superior frontal cortex (β EDSS ≤-0.09) and the pars orbitalis (β EDSS ≤-0.09).
Conclusion
Our findings indicate accelerated, early GM atrophy in people with RRMS, specific to the frontal lobes, which is more pronounced than in older HCs and uniquely related to disability-progression. These results suggest frontal lobe atrophy as an imaging biomarker in future MS-trials.
Key messages
What is already known on this topic
Grey matter atrophy is present in multiple sclerosis. The replicability of region-specific atrophy patterns has however not been systematically assessed, neither their relationship to different clinical outcomes, nor their comparison to healthy controls.
What this study adds
We present atrophy patterns with a dominant role of the frontal lobes, also presenting associations with disability progression. Additionally, we show that grey matter degenerates faster in people with multiple sclerosis than in more than 20 years older healthy controls.
How this study might affect research, practice or policy
Our findings highlight the presence of strong grey matter atrophy patterns in multiple sclerosis. Consequentially, more focus could be cast on cortical areas, and specifically the frontal lobes, when assessing neurodegeneration and disease progression in multiple sclerosis.
