Pulsatile Brain Motion as a Marker of Brain Aging and Dementia: Insights from 3D q-aMRI

Heart-brain interactions, including cardiac-induced brain pulsatility, are thought to support brain homeostasis, yet their alteration with aging and neurodegeneration remains poorly understood. Here, we used three-dimensional quantitative amplified MRI (q-aMRI) to visualize and quantify cardiac-induced pulsatile brain motion across healthy individuals and those on the Alzheimer's and Lewy body disease spectra. Expert evaluations revealed consistent distinctions between normal and abnormal motion patterns, which were further characterized using strain-based biomechanical features. Principal component analysis identified interpretable signatures of abnormal motion that emerged predominantly after midlife and were closely linked to chronological age. Even after accounting for age, these biomechanical features differentiated individuals with clinical and biomarker evidence of neurodegenerative disease. Together, these findings suggest that q-aMRI-derived measures of cardiac-gated pulsatile brain motion may serve as imaging biomarkers of normal brain aging and dementia.

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Publication Details

Journal
medRxiv
Published
2025-12-11
DOI
https://doi.org/10.64898/2025.12.10.25341649
Primary Topic
Functional Brain Connectivity Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Pulsatile Brain Motion as a Marker of Brain Aging and Dementia: Insights from 3D q-aMRI

Samantha J. Holdsworth, Kyan Younes, Itamar Terem, Paul Condron et al.
medRxiv
Functional Brain Connectivity Studies
article

Pulsatile Brain Motion as a Marker of Brain Aging and Dementia: Insights from 3D q-aMRI

Samantha J. Holdsworth, Kyan Younes, Itamar Terem, Paul Condron, Kathleen L. Poston, Elizabeth C. Mormino, Eryn Kwon, Daniel Cornfeld, Kawin Setsompop, Hillary Vossler, J. T. M. Wright, Andrew Dreisbach
article en

Abstract

Heart-brain interactions, including cardiac-induced brain pulsatility, are thought to support brain homeostasis, yet their alteration with aging and neurodegeneration remains poorly understood. Here, we used three-dimensional quantitative amplified MRI (q-aMRI) to visualize and quantify cardiac-induced pulsatile brain motion across healthy individuals and those on the Alzheimer's and Lewy body disease spectra. Expert evaluations revealed consistent distinctions between normal and abnormal motion patterns, which were further characterized using strain-based biomechanical features. Principal component analysis identified interpretable signatures of abnormal motion that emerged predominantly after midlife and were closely linked to chronological age. Even after accounting for age, these biomechanical features differentiated individuals with clinical and biomarker evidence of neurodegenerative disease. Together, these findings suggest that q-aMRI-derived measures of cardiac-gated pulsatile brain motion may serve as imaging biomarkers of normal brain aging and dementia.

medRxiv
University of Auckland (NZ), Neurosciences Institute (US), Medical Research Institute of New Zealand (NZ), Brain Research New Zealand (NZ), Mātai Medical Research Institute, Stanford University (US)
National Science Foundation, Alzheimer's Association, Royal Society Te Apārangi, National Institutes of Health, Marsden Fund, National Institute on Aging
Openalex Percentile: Top 58%
Functional Brain Connectivity Studies
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