Microstructural white matter alterations in Alzheimer's disease and amnestic mild cognitive impairment and its

Tongtong Li1, Yu Zhang1, Xiuwei Fu2

  • 1First Central Clinical College, Tianjin Medical University, Tianjin, 300192, China.

Insights

Diffusion kurtosis imaging (DKI) reveals white matter microstructural changes in Alzheimer's disease (AD) and amnestic mild cognitive impairment (aMCI). Kurtosis fractional anisotropy (KFA) may be a sensitive marker for detecting these alterations.

Area of Science:

  • Neuroimaging
  • Neurology
  • Biomedical Engineering

Background:

  • Alzheimer's disease (AD) and amnestic mild cognitive impairment (aMCI) are characterized by progressive neurodegeneration.
  • White matter microstructural integrity is crucial for cognitive function and is often compromised in neurodegenerative diseases.
  • Diffusion kurtosis imaging (DKI) offers advanced insights into white matter microstructure beyond conventional diffusion tensor imaging (DTI).

Purpose of the Study:

  • To investigate white matter microstructural alterations in AD and aMCI using DKI.
  • To compare DKI-derived parameters between AD patients, aMCI patients, and healthy controls (HC).
  • To assess the diagnostic performance of DKI parameters in differentiating between these groups and their correlation with cognitive scores.

Main Methods:

  • Prospective study involving 45 AD patients, 42 aMCI patients, and 35 HC.
  • Diffusion-weighted images acquired and analyzed using Tract-based Spatial Statistics (TBSS) with DKI.
  • Evaluated parameters: kurtosis fractional anisotropy (KFA), mean kurtosis (MK), fractional anisotropy (FA), and mean diffusivity (MD).
  • Correlations with Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA) scores analyzed.
  • Receiver operating characteristic (ROC) curve analysis performed for diagnostic evaluation.

Main Results:

  • Significant decrease in KFA observed in aMCI patients compared to HC.
  • Significant decreases in FA, KFA, and MK, and a significant increase in MD were found in AD patients compared to both HC and aMCI groups.
  • Many white matter tracts showed significant correlations between DKI parameters (FA, MD, KFA, MK) and MMSE/MoCA scores.
  • Highest diagnostic performance (Area Under the Curve - AUC) for aMCI and AD detection was achieved with KFA values in the splenium of the corpus callosum.

Conclusions:

  • White matter microstructure compactness and complexity are reduced in AD and aMCI.
  • DKI parameters, particularly KFA, show promise for detecting white matter alterations in AD and aMCI.
  • DKI can provide valuable information regarding the severity and progression of Alzheimer's disease.