Reconstruction of respiratory variation signals from fMRI data

Functional MRI signals can be heavily influenced by systemic physiological processes in addition to local neural activity. For example, widespread hemodynamic fluctuations across the brain have been found to correlate with natural, low-frequency variations in the depth and rate of breathing over time. Acquiring peripheral measures of respiration during fMRI scanning not only allows for modeling such effects in fMRI analysis, but also provides valuable information for interrogating brain-body physiology. However, physiological recordings are frequently unavailable or have insufficient quality. Here, we propose a computational technique for reconstructing continuous low-frequency respiration volume (RV) fluctuations from fMRI data alone. We evaluate the performance of this approach across different fMRI preprocessing strategies. Further, we demonstrate that the predicted RV signals can account for similar patterns of temporal variation in resting-state fMRI data compared to measured RV fluctuations. These findings indicate that fluctuations in respiration volume can be extracted from fMRI alone, in the common scenario of missing or corrupted respiration recordings. The results have implications for enriching a large volume of existing fMRI datasets through retrospective addition of respiratory variations information.

[1]  Catie Chang,et al.  Sympathetic activity contributes to the fMRI signal , 2019, Communications Biology.

[2]  Marko Sarlija,et al.  A convolutional neural network based approach to QRS detection , 2017, Proceedings of the 10th International Symposium on Image and Signal Processing and Analysis.

[3]  César Caballero-Gaudes,et al.  Methods for cleaning the BOLD fMRI signal , 2016, NeuroImage.

[4]  G H Glover,et al.  Image‐based method for retrospective correction of physiological motion effects in fMRI: RETROICOR , 2000, Magnetic resonance in medicine.

[5]  Catie Chang,et al.  Resting-state “physiological networks” , 2019, NeuroImage.

[6]  Kevin Murphy,et al.  Resting-state fMRI confounds and cleanup , 2013, NeuroImage.

[7]  Kevin Murphy,et al.  Robustly measuring vascular reactivity differences with breath-hold: Normalising stimulus-evoked and resting state BOLD fMRI data , 2011, NeuroImage.

[8]  Emery N. Brown,et al.  Model-based physiological noise removal in fast fMRI , 2020, NeuroImage.

[9]  G. Glover,et al.  Correction of physiologically induced global off‐resonance effects in dynamic echo‐planar and spiral functional imaging , 2002, Magnetic resonance in medicine.

[10]  Han Yuan,et al.  Correlated slow fluctuations in respiration, EEG, and BOLD fMRI , 2013, NeuroImage.

[11]  Catie Chang,et al.  Mapping the end-tidal CO2 response function in the resting-state BOLD fMRI signal: Spatial specificity, test–retest reliability and effect of fMRI sampling rate , 2015, NeuroImage.

[12]  Serdar Aslan,et al.  Extraction of the cardiac waveform from simultaneous multislice fMRI data using slice sorted averaging and a deep learning reconstruction filter , 2019, NeuroImage.

[13]  Steen Moeller,et al.  ICA-based artefact removal and accelerated fMRI acquisition for improved resting state network imaging , 2014, NeuroImage.

[14]  R. Turner,et al.  Detecting Latency Differences in Event-Related BOLD Responses: Application to Words versus Nonwords and Initial versus Repeated Face Presentations , 2002, NeuroImage.

[15]  Stephen M. Smith,et al.  Temporally-independent functional modes of spontaneous brain activity , 2012, Proceedings of the National Academy of Sciences.

[16]  Catie Chang,et al.  Corrigendum to “Mapping the end-tidal CO2 response function in the resting-state BOLD fMRI signal: Spatial specificity, test-retest reliability and effect of fMRI sampling rate.” , 2018, NeuroImage.

[17]  Kevin Murphy,et al.  Vascular physiology drives functional brain networks , 2018, NeuroImage.

[18]  Stephen M. Smith,et al.  Using temporal ICA to selectively remove global noise while preserving global signal in functional MRI data , 2017, NeuroImage.

[19]  Catie Chang,et al.  Influence of heart rate on the BOLD signal: The cardiac response function , 2009, NeuroImage.

[20]  Kevin Murphy,et al.  Cleaning up the fMRI time series: Mitigating noise with advanced acquisition and correction strategies , 2017, NeuroImage.

[21]  Peter A. Bandettini,et al.  The respiration response function: The temporal dynamics of fMRI signal fluctuations related to changes in respiration , 2008, NeuroImage.

[22]  Xenophon Papademetris,et al.  Groupwise whole-brain parcellation from resting-state fMRI data for network node identification , 2013, NeuroImage.

[23]  Catie Chang,et al.  A Deep Pattern Recognition Approach for Inferring Respiratory Volume Fluctuations from fMRI Data , 2020, MICCAI.

[24]  Wen-Ming Luh,et al.  Differentiating BOLD and non-BOLD signals in fMRI time series using multi-echo EPI , 2012, NeuroImage.

[25]  Mark D'Esposito,et al.  Variation of BOLD hemodynamic responses across subjects and brain regions and their effects on statistical analyses , 2004, NeuroImage.

[26]  Hazem H. Refai,et al.  Subject specific BOLD fMRI respiratory and cardiac response functions obtained from global signal , 2013, NeuroImage.

[27]  Irene Tracey,et al.  Resting fluctuations in arterial carbon dioxide induce significant low frequency variations in BOLD signal , 2004, NeuroImage.

[28]  F. H. Lopes da Silva,et al.  A study of the brain's resting state based on alpha band power, heart rate and fMRI , 2008, NeuroImage.

[29]  John Suckling,et al.  Detection of physiological noise in resting state fMRI using machine learning , 2013, Human brain mapping.

[30]  Jonathan D. Power,et al.  Distinctions among real and apparent respiratory motions in human fMRI data , 2019, NeuroImage.

[31]  Yunjie Tong,et al.  Perfusion information extracted from resting state functional magnetic resonance imaging , 2017, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[32]  Yunjie Tong,et al.  Tracking cerebral blood flow in BOLD fMRI using recursively generated regressors , 2014, Human brain mapping.

[33]  Mark Jenkinson,et al.  The minimal preprocessing pipelines for the Human Connectome Project , 2013, NeuroImage.

[34]  J. Jean Chen,et al.  Quantitative mapping of cerebrovascular reactivity using resting-state BOLD fMRI: Validation in healthy adults , 2016, NeuroImage.

[35]  Timothy O. Laumann,et al.  Sources and implications of whole-brain fMRI signals in humans , 2017, NeuroImage.

[36]  Stephen M. Smith,et al.  Classification of temporal ICA components for separating global noise from fMRI data: Reply to Power , 2019, NeuroImage.

[37]  Jeff H. Duyn,et al.  Characterization of regional heterogeneity in cerebrovascular reactivity dynamics using novel hypocapnia task and BOLD fMRI , 2009, NeuroImage.

[38]  D. Picchioni,et al.  Sympathetic activity contributes to the fMRI signal , 2019, Communications Biology.

[39]  Lia M Hocke,et al.  Post‐hoc physiological waveform extraction from motion estimation in simultaneous multislice (SMS) functional MRI using separate stack processing , 2020, Magnetic resonance in medicine.

[40]  Bruce R. Rosen,et al.  Resting-state “physiological networks” , 2019, NeuroImage.

[41]  Georgios D. Mitsis,et al.  Identification of physiological response functions to correct for fluctuations in resting-state fMRI related to heart rate and respiration , 2019, NeuroImage.

[42]  M. Greicius,et al.  Decoding subject-driven cognitive states with whole-brain connectivity patterns. , 2012, Cerebral cortex.

[43]  Yunjie Tong,et al.  Low-frequency oscillations measured in the periphery with near-infrared spectroscopy are strongly correlated with blood oxygen level-dependent functional magnetic resonance imaging signals , 2012, Journal of biomedical optics.

[44]  Catie Chang,et al.  Physiological changes in sleep that affect fMRI inference , 2020, Current Opinion in Behavioral Sciences.

[45]  Jonathan D. Power,et al.  Distinctions among real and apparent respiratory motions in human fMRI data , 2019, NeuroImage.

[46]  Catie Chang,et al.  Mapping and correction of vascular hemodynamic latency in the BOLD signal , 2008, NeuroImage.

[47]  Mark J. Lowe,et al.  Isolating physiologic noise sources with independently determined spatial measures , 2007, NeuroImage.

[48]  R G Wise,et al.  Spontaneous physiological variability modulates dynamic functional connectivity in resting-state functional magnetic resonance imaging , 2016, Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.

[49]  Ewald Moser,et al.  On the origin of respiratory artifacts in BOLD-EPI of the human brain. , 2002, Magnetic resonance imaging.

[50]  Essa Yacoub,et al.  The WU-Minn Human Connectome Project: An overview , 2013, NeuroImage.

[51]  P. Bandettini,et al.  The effect of respiration variations on independent component analysis results of resting state functional connectivity , 2008, Human brain mapping.

[52]  Martín Abadi,et al.  TensorFlow: Large-Scale Machine Learning on Heterogeneous Distributed Systems , 2016, ArXiv.

[53]  Vascular physiology drives functional brain networks , 2020, NeuroImage.

[54]  Peter A. Bandettini,et al.  Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI , 2006, NeuroImage.

[55]  Georgios D. Mitsis,et al.  Identification of physiological response functions to correct for fluctuations in resting-state fMRI related to heart rate and respiration , 2019, NeuroImage.