Open AccessIntracranial arterial four‐dimensional flow is associated with metrics of brain health and Alzheimer's disease
Author(s) -
Berman Sara E.,
RiveraRivera Leonardo A.,
Clark Lindsay R.,
Racine Annie M.,
Keevil Jon G.,
Bratzke Lisa C.,
Carlsson Cynthia M.,
Bendlin Barbara B.,
Rowley Howard A.,
Blennow Kaj,
Zetterberg Henrik,
Asthana Sanjay,
Turski Patrick,
Johnson Sterling C.,
Wieben Oliver
Publication year - 2015
Publication title -
alzheimer's and dementia: diagnosis, assessment and disease monitoring
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.497
H-Index - 37
ISSN - 2352-8729
DOI - 10.1016/j.dadm.2015.09.005
Subject(s) - medicine , atrophy , cerebral blood flow , circle of willis , magnetic resonance imaging , cardiology , cerebrospinal fluid , cerebral arteries , pathological , anterior cerebral artery , cerebral atrophy , biomarker , middle cerebral artery , disease , pathology , radiology , ischemia , biochemistry , chemistry
Although cerebrovascular disease has long been known to co‐occur with Alzheimer's disease (AD), recent studies suggest an etiologic contribution to AD pathogenesis. We used four dimensional (4D)‐flow magnetic resonance imaging (MRI) to evaluate blood flow and pulsatility indices in the circle of Willis. We hypothesized decreased mean blood flow and increased pulsatility, metrics indicative of poor vascular health, would be associated with cerebral atrophy and an AD cerebrospinal fluid (CSF) profile. Methods A total of 312 patients along the AD continuum (172 middle aged, 60 cognitively healthy older, 44 mild cognitive impairment, and 36 AD) underwent MRI, CSF, and medical examinations. Regression was used to predict CSF biomarkers and atrophy from 4D‐flow and analysis of covariance to compare vascular health between groups. Results Decreased mean flow in the middle cerebral artery (MCA) and superior portion of the internal carotid artery (sICA) and increased pulsatility in the MCA were associated with greater brain atrophy. Decreased mean flow in the sICA was associated with lower amyloid beta 1–42 (Aβ 42 ) in the CSF, a pathologic biomarker profile associated with AD. Interestingly, although metrics of flow and pulsatility differed markedly across the AD spectrum, there were no significant differences in cardiovascular risk score, mean arterial pressure, and pulse pressure across the three age‐matched older cohorts. Discussion By measuring intracranial arterial health directly with 4D‐flow MRI, these data suggest that intracranial arterial health is compromised in symptomatic AD. Even after accounting for disease stage, cerebral artery health is associated with atrophy and an AD Aβ 42 profile, suggesting neurovascular health may contribute to the etiopathogenesis of AD.