Microbleeds in postmortem brains of patients with Alzheimer disease: a T2*-weighted gradient-echo 7.0 T magnetic

Jacques L De Reuck1, Charlotte Cordonnier, Vincent Deramecourt

  • 1Université Lille Nord de France, UDSL, EA 1046, Lille University Hospital, Lille, France. dereuck.j@gmail.com

Insights

This study investigated microbleeds (MBs) in Alzheimer disease (AD) brains using 7.0 T MRI. MBs distribution varied based on the presence of severe cerebral amyloid angiopathy (CAA) in AD patients.

Area of Science:

  • Neuroimaging
  • Neuropathology
  • Alzheimer Disease Research

Background:

  • Alzheimer disease (AD) is a neurodegenerative disorder characterized by amyloid plaques and neurofibrillary tangles.
  • Microbleeds (MBs) are common in neurodegenerative diseases, but their distribution in AD, particularly with comorbid cerebral amyloid angiopathy (CAA), requires further investigation.
  • High-field MRI offers enhanced visualization of neuroimaging biomarkers like MBs.

Purpose of the Study:

  • To determine and quantify the distribution of microbleeds (MBs) in postmortem Alzheimer disease (AD) brains.
  • To compare MB distribution in AD brains with and without severe cerebral amyloid angiopathy (AD-CAA).
  • To assess MB prevalence across different cortical layers and anatomical regions.

Main Methods:

  • Postmortem brains from 28 Alzheimer disease (AD) patients and 5 controls were analyzed.
  • T2*-weighted gradient-echo 7.0 Tesla magnetic resonance imaging (MRI) was employed.
  • Microbleeds (MBs) were quantified and their distribution assessed on coronal sections at frontal, central, and occipital levels, and within cortical layers.

Main Results:

  • Microbleeds (MBs) were more prevalent in central sections of AD brains without severe cerebral amyloid angiopathy (CAA).
  • In AD-CAA brains, MBs were more frequent across all coronal sections compared to AD brains without CAA.
  • MBs were significantly increased in all cortical layers of AD-CAA brains compared to controls, and prevailed in deep cortical layers of AD brains and controls.

Conclusions:

  • The topographic distribution of microbleeds (MBs) in Alzheimer disease (AD) brains differs based on the presence or absence of severe cerebral amyloid angiopathy (CAA).
  • High-field MRI is effective in characterizing microbleed patterns in AD neuropathology.
  • Understanding MB distribution may offer insights into AD pathogenesis and progression, especially when complicated by CAA.

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