Prospective Longitudinal Perfusion in Probable Alzheimer's Disease Correlated with Atrophy in Temporal Lobe

Tony D Zhou1, Zongpai Zhang2, Arvind Balachandrasekaran3

  • 1Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, MO 63110, USA.

Aging and Disease
|May 17, 2023
PubMed

Insights

Reduced cerebral blood flow (CBF) may cause brain atrophy in Alzheimer's disease (AD) and mild cognitive impairment (MCI). This study investigated the link between CBF and gray matter volumes (GMVs), finding hypoperfusion might precede atrophy in the temporal pole.

Area of Science:

  • Neuroimaging
  • Neurology
  • Gerontology

Background:

  • Mild cognitive impairment (MCI) and Alzheimer's disease (AD) are associated with reduced cerebral blood flow (CBF) and gray matter volumes (GMVs).
  • The temporal relationship between these reductions is not fully understood.

Purpose of the Study:

  • To determine if reduced CBF leads to reduced GMVs or vice versa.
  • To investigate the temporal sequence of hypoperfusion and atrophy in neurodegenerative conditions.

Main Methods:

  • Analysis of perfusion and structural MRI data from 148 participants (normal controls, MCI, AD) in the Cardiovascular Health Study Cognition Study (CHS-CS).
  • Longitudinal assessment of GMVs and CBF over time (Time 1, Time 2, Time 3).
  • Statistical investigation of associations between GMVs and subsequent CBF changes, and vice versa.

Main Results:

  • Alzheimer's disease patients showed smaller temporal pole GMVs compared to normal controls and MCI at Time 2.
  • Reduced temporal pole GMVs at Time 2 were associated with subsequent CBF declines in the temporal pole and temporoparietal regions.
  • Reduced hippocampal GMVs were linked to subsequent temporoparietal CBF declines.
  • Temporal pole CBF at Time 2 predicted subsequent GMV changes in the same region.

Conclusions:

  • Hypoperfusion in the temporal pole may be an early event that drives subsequent gray matter atrophy.
  • CBF declines in the temporoparietal and temporal pole regions appear to follow atrophy in the temporal pole.