Volumetric alterations of hippocampal and amygdala subfields in Azheimer's disease

Qi Feng1, Zhehao Zhang2,3, Fengyi Dai2,4

  • 1Department of Radiology, Affiliated Hangzhou First People's Hospital, Westlake University School of Medicine, Hangzhou, P.R. China.

BMC Medical Imaging
|September 27, 2025
PubMed
Abstract

Insights

Volume reduction in specific hippocampus subfields is linked to cognitive decline in Alzheimer's disease (AD) and amnestic mild cognitive impairment (aMCI). This MRI study highlights potential biomarkers for early detection and monitoring of these neurodegenerative conditions.

Area of Science:

  • Neuroimaging
  • Neurodegeneration
  • Cognitive Neuroscience

Background:

  • Alzheimer's disease (AD) and amnestic mild cognitive impairment (aMCI) are associated with hippocampal and amygdala atrophy.
  • Limited research has jointly analyzed volumes of hippocampal and amygdala subfields using MRI.

Purpose of the Study:

  • To investigate volumetric differences in hippocampal and amygdala subfields in patients with AD and aMCI compared to controls.
  • To explore correlations between subfield volumes and cognitive scores.

Main Methods:

  • Cross-sectional study utilizing analysis of covariance (ANCOVA).
  • Analyzed volumes of 19 hippocampal and 9 amygdala subfields in 40 normal controls (NC), 40 aMCI, and 53 AD patients.
  • Correlated significant subfield volume differences with overall cognitive scores (MMSE, MoCA).

Main Results:

  • Significant atrophy observed in 16 hippocampal subfields across the three groups, predominantly in the right hemisphere.
  • No significant volume loss detected in amygdalar subfields after multiple-testing correction.
  • Positive correlation found between volumes of certain hippocampal subfields and MMSE/MoCA scores.

Conclusions:

  • Volume reduction in specific hippocampal subfields may serve as a potential imaging biomarker for cognitive decline in AD and aMCI.
  • These findings contribute to understanding the neuroanatomical basis of cognitive impairment in AD and aMCI.