Post-mortem cohort study reveals reduced amyloid beta and neurofibrillary tangles in multiple sclerosis cortex, suggesting disease-specific factors influence pathological protein clearance.
Multiple sclerosis (MS) and Alzheimer's disease (AD) are neurodegenerative diseases demonstrating age-related accumulation of disability. Inflammation lasting decades is a paradigmatic feature of MS pathology that variably relates to neurodegeneration, while the accumulation of Amyloid-beta (A-beta) plaques and neurofibrillary tangles (NFT) are cornerstones of AD pathology. However, few studies investigated the accumulation of amyloids in MS. We investigated A-beta deposition and NFT density in temporal or frontal cortices derived from a large post-mortem cohort of MS (n=78) and age and sex-matched control (n=65) cases. We found reduced A-beta burden in MS cases compared with controls in particular in cases below 65 years of age. NFT was similarly reduced in MS compared to controls, in particular in cases above 65 years of age. Higher A-beta expression predicted greater NFT density in MS. These findings suggest that MS-related factors may influence A-beta and NFT deposition and/or clearance. This work highlights new therapeutic perspectives relevant for both MS and AD.
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Pansieri et al. (2024) studied this question.
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