Distinct patterns of microstructural brain changes in Alzheimer's disease subtypes: Diffusion MRI metrics in braak

Naoki Hayakawa1, Shuko Takeda2,3, Hiroto Takahashi4

  • 1Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Insights

Alzheimer's disease (AD) subtypes show distinct brain microstructural changes. Hippocampal-sparing AD preserves hippocampal integrity, unlike typical AD, indicating varied disease progression patterns.

Area of Science:

  • Neuroimaging
  • Neuropathology
  • Brain Microstructure Analysis

Background:

  • Alzheimer's disease (AD) is characterized by amyloid-beta and tau accumulation, leading to neuronal death.
  • Neuropathological changes follow a Braak staging pattern, typically starting in the medial temporal lobe.
  • Distinct AD subtypes, including hippocampal-sparing (HpSp) AD, exhibit varying patterns of neuropathology.

Purpose of the Study:

  • To investigate the microstructural differences between typical AD and HpSp AD using Neurite Orientation Dispersion and Density Imaging (NODDI).
  • To identify specific brain regions affected differently in AD subtypes.

Main Methods:

  • Individuals with mild cognitive impairment and positive AD cerebrospinal fluid markers were classified into typical AD and HpSp AD groups based on MRI.
  • Regions of interest were defined in Braak stage-related areas: hippocampus, precuneus, and postcentral gyrus.
  • NODDI metrics (intracellular volume fraction, orientation dispersion index, isotropic volume fraction) were compared across groups.

Main Results:

  • Significant differences in hippocampal NODDI metrics were observed between typical AD and HpSp AD.
  • HpSp AD showed hippocampal NODDI values comparable to non-AD controls.
  • Higher isotropic volume fraction (Viso) was found in the precuneus of HpSp AD compared to typical AD.

Conclusions:

  • AD subtypes exhibit distinct patterns of brain microstructural alterations in Braak stage-related regions.
  • HpSp AD is characterized by preserved hippocampal microstructure compared to typical AD.
  • These findings highlight the utility of NODDI in differentiating AD subtypes and understanding their unique neuropathological profiles.