Unexpected Low Rate of Amyloid-β Pathology in Multiple Sclerosis Patients

Matthew R Brier1,2, Suzanne E Schindler1, Amber Salter3

  • 1Department of Neurology, Washington University in St. Louis, St. Louis, MO, USA.

Annals of Neurology
|July 4, 2024
PubMed

Insights

Multiple sclerosis (MS) patients show a lower prevalence of Alzheimer disease pathology, specifically amyloid-β biomarkers. This suggests that MS may offer protection against developing Alzheimer disease.

Area of Science:

  • Neurology
  • Neuroimmunology
  • Neurodegenerative Diseases

Background:

  • Increasing life expectancy in multiple sclerosis (MS) necessitates understanding co-occurring health conditions.
  • Atypical presentation of Alzheimer disease dementia in MS patients prompted further investigation.
  • Alzheimer disease pathology is characterized by amyloid-β accumulation.

Purpose of the Study:

  • To investigate the prevalence of Alzheimer disease pathology in patients with multiple sclerosis.
  • To determine if MS is associated with a reduced risk of Alzheimer disease.

Main Methods:

  • Compared amyloid-β plasma biomarker positivity rates between 100 MS patients and 300 matched non-MS controls.
  • Controlled for age, sex, apolipoprotein E proteotype, and cognitive status in the comparison groups.
  • Examined the clinical features of MS patients with positive amyloid-β biomarker results.

Main Results:

  • Amyloid-β plasma biomarker positivity was approximately half as common in MS patients compared to controls.
  • MS patients with detected amyloid-β pathology often presented with atypical features at diagnosis.
  • These findings indicate a potential protective association between MS and Alzheimer disease.

Conclusions:

  • Multiple sclerosis is associated with a reduced risk of developing Alzheimer disease.
  • The study suggests novel research directions into the interplay between MS and Alzheimer disease pathogenesis.
  • Understanding this relationship may lead to new therapeutic strategies for both conditions.