Mild cognitive impairment with Lewy bodies: blood perfusion with arterial spin labelling

Michael J Firbank1, John T O'Brien2, Rory Durcan3

  • 1Translational and Clinical Research Institute, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, NE4 5PL, UK. michael.firbank@ncl.ac.uk.

Journal of Neurology
|October 21, 2020
PubMed
Abstract

Insights

Mild cognitive impairment with Lewy bodies (MCI-LB) shows distinct perfusion differences compared to Alzheimer

Area of Science:

  • Neuroimaging
  • Neurology
  • Medical Imaging

Background:

  • Mild cognitive impairment (MCI) encompasses various subtypes, including MCI with Lewy bodies (MCI-LB) and MCI of the Alzheimer's type (MCI-AD).
  • Distinguishing between these subtypes is crucial for accurate diagnosis and management.
  • Cerebral perfusion imaging offers a potential method for identifying distinct pathological patterns.

Purpose of the Study:

  • To investigate differences in cerebral perfusion between individuals with MCI-LB, MCI-AD, and healthy controls using arterial spin labelling (ASL).
  • To identify specific perfusion patterns associated with MCI-LB.

Main Methods:

  • Arterial spin labelling (ASL) perfusion imaging was performed on 32 MCI-LB, 30 MCI-AD, and 28 healthy control subjects.
  • Relative perfusion was calculated with respect to the cerebellum.
  • Voxelwise comparisons and region-of-interest analyses (occipital/medial temporal, posterior cingulate/precuneus) were conducted.

Main Results:

  • MCI-LB subjects exhibited reduced perfusion in posterior parietal and occipital regions compared to controls.
  • The occipital to medial temporal perfusion ratio was significantly lower in MCI-LB.
  • The posterior cingulate to precuneus perfusion ratio was significantly higher in MCI-LB.

Conclusions:

  • MCI-LB demonstrates unique patterns of altered cerebral perfusion.
  • These perfusion alterations in MCI-LB resemble those observed in dementia with Lewy bodies.
  • ASL imaging may aid in differentiating MCI subtypes based on perfusion deficits.