4.5 Article

Diffusion tensor tractography of the fornix in cerebral amyloid angiopathy, mild cognitive impairment and Alzheimer's disease

Journal

NEUROIMAGE-CLINICAL
Volume 34, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2022.103002

Keywords

Cerebral amyloid angiopathy; Alzheimer's disease; Mild cognitive impairment; Diffusion tensor imaging; Fornix; Cognition

Categories

Funding

  1. Canadian Consortium on Neuro-degeneration of Aging (CIHR)
  2. Canadian Institutes of Health Research [MOP-142175, FDN-154317]
  3. Brain Canada, Canadian Stroke Network [MIRI2015-3994]
  4. Canadian Stroke Network
  5. Heart and Stroke Foundation of Alberta
  6. Alzheimer Society of Canada
  7. Canada Research Chairs program

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Diffusion tensor imaging metrics of the fornix were compared between patients with cerebral amyloid angiopathy (CAA), Alzheimer's disease (AD), Mild Cognitive Impairment (MCI), and healthy controls. The study found significant diffusion changes in the fornix of CAA, AD, and MCI patients compared to controls, suggesting differences in the mechanisms of fornix diffusion abnormalities between CAA and AD/MCI.
Purpose: Cerebral amyloid angiopathy (CAA) is a common neuropathological finding and clinical entity that occurs independently and with co-existent Alzheimer's disease (AD) and small vessel disease. We compared diffusion tensor imaging (DTI) metrics of the fornix, the primary efferent tract of the hippocampus between CAA, AD and Mild Cognitive Impairment (MCI) and healthy controls. Methods: Sixty-eight healthy controls, 32 CAA, 21 AD, and 26 MCI patients were recruited at two centers. Diffusion tensor images were acquired at 3 T with high spatial resolution and fluid-attenuated inversion recovery (FLAIR) to suppress cerebrospinal fluid (CSF) and minimize partial volume effects on the fornix. The fornix was delineated with deterministic tractography to yield mean diffusivity (MD), axial diffusivity (AXD), radial diffusivity (RD), fractional anisotropy (FA) and tract volume. Volumetric measurements of the hippocampus, thalamus, and lateral ventricles were obtained using T1-weighted MRI. Results: Diffusivity (MD, AXD, and RD) of the fornix was highest in AD followed by CAA compared to controls; the MCI group was not significantly different from controls. FA was similar between groups. Fornix tract volume was ~ 30% lower for all three patient groups compared to controls, but not significantly different between the patient groups. Thalamic and hippocampal volumes were preserved in CAA, but lower in AD and MCI compared to controls. Lateral ventricular volumes were increased in CAA, AD and MCI. Global cognition, memory, and executive function all correlated negatively with fornix diffusivity across the combined clinical group. Conclusion: There were significant diffusion changes of the fornix in CAA, AD and MCI compared to controls, despite relatively intact thalamic and hippocampal volumes in CAA, suggesting the mechanisms for fornix diffusion abnormalities may differ in CAA compared to AD and MCI.

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