Cargando…

Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI

Resting-state functional magnetic resonance imaging (rs-fMRI) is a widely used technique for mapping the brain’s functional architecture, so delineating the main sources of variance comprising the signal is crucial. Low frequency oscillations (LFO) that are not of neural origin, but which are driven...

Descripción completa

Detalles Bibliográficos
Autores principales: Whittaker, Joseph R., Driver, Ian D., Venzi, Marcello, Bright, Molly G., Murphy, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514145/
https://www.ncbi.nlm.nih.gov/pubmed/31133780
http://dx.doi.org/10.3389/fnins.2019.00433
_version_ 1783417835734695936
author Whittaker, Joseph R.
Driver, Ian D.
Venzi, Marcello
Bright, Molly G.
Murphy, Kevin
author_facet Whittaker, Joseph R.
Driver, Ian D.
Venzi, Marcello
Bright, Molly G.
Murphy, Kevin
author_sort Whittaker, Joseph R.
collection PubMed
description Resting-state functional magnetic resonance imaging (rs-fMRI) is a widely used technique for mapping the brain’s functional architecture, so delineating the main sources of variance comprising the signal is crucial. Low frequency oscillations (LFO) that are not of neural origin, but which are driven by mechanisms related to cerebral autoregulation (CA), are present in the blood-oxygenation-level-dependent (BOLD) signal within the rs-fMRI frequency band. In this study we use a MR compatible device (Caretaker, Biopac) to obtain a non-invasive estimate of beat-to-beat mean arterial pressure (MAP) fluctuations concurrently with rs-fMRI at 3T. Healthy adult subjects (n = 9; 5 male) completed two 20-min rs-fMRI scans. MAP fluctuations were decomposed into different frequency scales using a discrete wavelet transform, and oscillations at approximately 0.1 Hz show a high degree of spatially structured correlations with matched frequency fMRI fluctuations. On average across subjects, MAP fluctuations at this scale of the wavelet decomposition explain ∼2.2% of matched frequency fMRI signal variance. Additionally, a simultaneous multi-slice multi-echo acquisition was used to collect 10-min rs-fMRI at three echo times at 7T in a separate group of healthy adults (n = 5; 5 male). Multiple echo times were used to estimate the R(2)(∗) decay at every time point, and MAP was shown to strongly correlate with this signal, which suggests a purely BOLD (i.e., blood flow related) origin. This study demonstrates that there is a significant component of the BOLD signal that has a systemic physiological origin, and highlights the fact that not all localized BOLD signal changes necessarily reflect blood flow supporting local neural activity. Instead, these data show that a proportion of BOLD signal fluctuations in rs-fMRI are due to localized control of blood flow that is independent of local neural activity, most likely reflecting more general systemic autoregulatory processes. Thus, fMRI is a promising tool for studying flow changes associated with cerebral autoregulation with high spatial resolution.
format Online
Article
Text
id pubmed-6514145
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-65141452019-05-27 Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI Whittaker, Joseph R. Driver, Ian D. Venzi, Marcello Bright, Molly G. Murphy, Kevin Front Neurosci Neuroscience Resting-state functional magnetic resonance imaging (rs-fMRI) is a widely used technique for mapping the brain’s functional architecture, so delineating the main sources of variance comprising the signal is crucial. Low frequency oscillations (LFO) that are not of neural origin, but which are driven by mechanisms related to cerebral autoregulation (CA), are present in the blood-oxygenation-level-dependent (BOLD) signal within the rs-fMRI frequency band. In this study we use a MR compatible device (Caretaker, Biopac) to obtain a non-invasive estimate of beat-to-beat mean arterial pressure (MAP) fluctuations concurrently with rs-fMRI at 3T. Healthy adult subjects (n = 9; 5 male) completed two 20-min rs-fMRI scans. MAP fluctuations were decomposed into different frequency scales using a discrete wavelet transform, and oscillations at approximately 0.1 Hz show a high degree of spatially structured correlations with matched frequency fMRI fluctuations. On average across subjects, MAP fluctuations at this scale of the wavelet decomposition explain ∼2.2% of matched frequency fMRI signal variance. Additionally, a simultaneous multi-slice multi-echo acquisition was used to collect 10-min rs-fMRI at three echo times at 7T in a separate group of healthy adults (n = 5; 5 male). Multiple echo times were used to estimate the R(2)(∗) decay at every time point, and MAP was shown to strongly correlate with this signal, which suggests a purely BOLD (i.e., blood flow related) origin. This study demonstrates that there is a significant component of the BOLD signal that has a systemic physiological origin, and highlights the fact that not all localized BOLD signal changes necessarily reflect blood flow supporting local neural activity. Instead, these data show that a proportion of BOLD signal fluctuations in rs-fMRI are due to localized control of blood flow that is independent of local neural activity, most likely reflecting more general systemic autoregulatory processes. Thus, fMRI is a promising tool for studying flow changes associated with cerebral autoregulation with high spatial resolution. Frontiers Media S.A. 2019-05-07 /pmc/articles/PMC6514145/ /pubmed/31133780 http://dx.doi.org/10.3389/fnins.2019.00433 Text en Copyright © 2019 Whittaker, Driver, Venzi, Bright and Murphy. http://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 Neuroscience
Whittaker, Joseph R.
Driver, Ian D.
Venzi, Marcello
Bright, Molly G.
Murphy, Kevin
Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI
title Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI
title_full Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI
title_fullStr Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI
title_full_unstemmed Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI
title_short Cerebral Autoregulation Evidenced by Synchronized Low Frequency Oscillations in Blood Pressure and Resting-State fMRI
title_sort cerebral autoregulation evidenced by synchronized low frequency oscillations in blood pressure and resting-state fmri
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514145/
https://www.ncbi.nlm.nih.gov/pubmed/31133780
http://dx.doi.org/10.3389/fnins.2019.00433
work_keys_str_mv AT whittakerjosephr cerebralautoregulationevidencedbysynchronizedlowfrequencyoscillationsinbloodpressureandrestingstatefmri
AT driveriand cerebralautoregulationevidencedbysynchronizedlowfrequencyoscillationsinbloodpressureandrestingstatefmri
AT venzimarcello cerebralautoregulationevidencedbysynchronizedlowfrequencyoscillationsinbloodpressureandrestingstatefmri
AT brightmollyg cerebralautoregulationevidencedbysynchronizedlowfrequencyoscillationsinbloodpressureandrestingstatefmri
AT murphykevin cerebralautoregulationevidencedbysynchronizedlowfrequencyoscillationsinbloodpressureandrestingstatefmri