Examining cerebrovascular burden across the cognitive continuum in older adults with and without evidence of amyloidosis
Background This work characterized cerebrovascular health in human subjects spanning the cognitive spectrum with and without presence of Aβ using different neuroimaging techniques (Fig1). Methods Subjects (n=70) were clinically characterized into four groups: cognitively unimpaired (CU), CU‐Declinin...
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Veröffentlicht in: | Alzheimer's & dementia 2022-12, Vol.18 (S1), p.n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
This work characterized cerebrovascular health in human subjects spanning the cognitive spectrum with and without presence of Aβ using different neuroimaging techniques (Fig1).
Methods
Subjects (n=70) were clinically characterized into four groups: cognitively unimpaired (CU), CU‐Declining (at‐risk of progressing to clinical mild MCI based on traditional neuropsychological data), clinical MCI, and clinical dementia (Fig2). MRI:
Vascular imaging: Whole‐brain 4D‐Flow data were acquired to characterize cerebrovascular health. pCASL with three post labeling delays was used to provide transit time corrected CBF maps. Structural imaging: T1‐weighted and T2‐FLAIR images were also collected for quantification of intracranial, hippocampal and white matter hyperintensity volumes. Hemodynamic measurements were extracted from intracranial arteries including the petrous ICAs, BA, MCAs, and veins SSS. Quantified flow parameters included: total cerebral blood flow, trans‐capillary pulse wave delay, and flow pulsatility index (PI). Trans‐capillary pulse wave delay was defined as the time shift between arterial and venous cardiac waveforms. PET: Aβ burden was assessed using 11C‐PiB PET imaging. Amyloid positivity (A‐, A+) was established as mean cortical PiB DVR >1.16. For A+ participants, amyloid time (i.e., estimated duration A+) was estimated using the sampled iterative local approximation algorithm. Differences were assessed using ANOVA followed by post‐hoc analysis (P |
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ISSN: | 1552-5260 1552-5279 |
DOI: | 10.1002/alz.063495 |