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Angiographic Pulse Wave Coherence in the Human Brain

A stroke volume of arterial blood that arrives to the brain housed in the rigid cranium must be matched over the cardiac cycle by an equivalent volume of ejected venous blood. We hypothesize that the brain maintains this equilibrium by organizing coherent arterial and venous pulse waves. To test thi...

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Autores principales: Koch, Matthew J., Duy, Phan Q., Grannan, Benjamin L., Patel, Aman B., Raymond, Scott B., Agarwalla, Pankaj K., Kahle, Kristopher T., Butler, William E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110661/
https://www.ncbi.nlm.nih.gov/pubmed/35592552
http://dx.doi.org/10.3389/fbioe.2022.873530
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author Koch, Matthew J.
Duy, Phan Q.
Grannan, Benjamin L.
Patel, Aman B.
Raymond, Scott B.
Agarwalla, Pankaj K.
Kahle, Kristopher T.
Butler, William E.
author_facet Koch, Matthew J.
Duy, Phan Q.
Grannan, Benjamin L.
Patel, Aman B.
Raymond, Scott B.
Agarwalla, Pankaj K.
Kahle, Kristopher T.
Butler, William E.
author_sort Koch, Matthew J.
collection PubMed
description A stroke volume of arterial blood that arrives to the brain housed in the rigid cranium must be matched over the cardiac cycle by an equivalent volume of ejected venous blood. We hypothesize that the brain maintains this equilibrium by organizing coherent arterial and venous pulse waves. To test this hypothesis, we applied wavelet computational methods to diagnostic cerebral angiograms in four human patients, permitting the capture and analysis of cardiac frequency phenomena from fluoroscopic images acquired at faster than cardiac rate. We found that the cardiac frequency reciprocal phase of a small region of interest (ROI) in a named artery predicts venous anatomy pixel-wise and that the predicted pixels reconstitute venous bolus passage timing. Likewise, a small ROI in a named vein predicts arterial anatomy and arterial bolus passage timing. The predicted arterial and venous pixel groups maintain phase complementarity across the bolus travel. We thus establish a novel computational method to analyze vascular pulse waves from minimally invasive cerebral angiograms and provide the first direct evidence of arteriovenous coupling in the intact human brain. This phenomenon of arteriovenous coupling may be a physiologic mechanism for how the brain precisely maintains mechanical equilibrium against volume displacement and kinetic energy transfer resulting from cyclical deformations with each heartbeat. The study also paves the way to study deranged arteriovenous coupling as an underappreciated pathophysiologic disturbance in a myriad of neurological pathologies linked by mechanical disequilibrium.
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spelling pubmed-91106612022-05-18 Angiographic Pulse Wave Coherence in the Human Brain Koch, Matthew J. Duy, Phan Q. Grannan, Benjamin L. Patel, Aman B. Raymond, Scott B. Agarwalla, Pankaj K. Kahle, Kristopher T. Butler, William E. Front Bioeng Biotechnol Bioengineering and Biotechnology A stroke volume of arterial blood that arrives to the brain housed in the rigid cranium must be matched over the cardiac cycle by an equivalent volume of ejected venous blood. We hypothesize that the brain maintains this equilibrium by organizing coherent arterial and venous pulse waves. To test this hypothesis, we applied wavelet computational methods to diagnostic cerebral angiograms in four human patients, permitting the capture and analysis of cardiac frequency phenomena from fluoroscopic images acquired at faster than cardiac rate. We found that the cardiac frequency reciprocal phase of a small region of interest (ROI) in a named artery predicts venous anatomy pixel-wise and that the predicted pixels reconstitute venous bolus passage timing. Likewise, a small ROI in a named vein predicts arterial anatomy and arterial bolus passage timing. The predicted arterial and venous pixel groups maintain phase complementarity across the bolus travel. We thus establish a novel computational method to analyze vascular pulse waves from minimally invasive cerebral angiograms and provide the first direct evidence of arteriovenous coupling in the intact human brain. This phenomenon of arteriovenous coupling may be a physiologic mechanism for how the brain precisely maintains mechanical equilibrium against volume displacement and kinetic energy transfer resulting from cyclical deformations with each heartbeat. The study also paves the way to study deranged arteriovenous coupling as an underappreciated pathophysiologic disturbance in a myriad of neurological pathologies linked by mechanical disequilibrium. Frontiers Media S.A. 2022-05-03 /pmc/articles/PMC9110661/ /pubmed/35592552 http://dx.doi.org/10.3389/fbioe.2022.873530 Text en Copyright © 2022 Koch, Duy, Grannan, Patel, Raymond, Agarwalla, Kahle and Butler. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Koch, Matthew J.
Duy, Phan Q.
Grannan, Benjamin L.
Patel, Aman B.
Raymond, Scott B.
Agarwalla, Pankaj K.
Kahle, Kristopher T.
Butler, William E.
Angiographic Pulse Wave Coherence in the Human Brain
title Angiographic Pulse Wave Coherence in the Human Brain
title_full Angiographic Pulse Wave Coherence in the Human Brain
title_fullStr Angiographic Pulse Wave Coherence in the Human Brain
title_full_unstemmed Angiographic Pulse Wave Coherence in the Human Brain
title_short Angiographic Pulse Wave Coherence in the Human Brain
title_sort angiographic pulse wave coherence in the human brain
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110661/
https://www.ncbi.nlm.nih.gov/pubmed/35592552
http://dx.doi.org/10.3389/fbioe.2022.873530
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