4.7 Article

Identification of physiological response functions to correct for fluctuations in resting-state fMRI related to heart rate and respiration

期刊

NEUROIMAGE
卷 202, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2019.116150

关键词

Physiological confounds; Cardiac activity; Breathing; fMRI artifacts; Physiological noise correction

资金

  1. Natural Sciences and Engineering Research Council of Canada [34362]
  2. Fonds de la Recherche du Quebec - Nature et Technologies (FRQNT) [PR191780-2016]
  3. Canada First Research Excellence Fund
  4. Quebec Bio-imaging Network (QBIN)
  5. 16 NIH Institutes and Centers [1U54MH091657]
  6. McDonnell Center for Systems Neuroscience at Washington University

向作者/读者索取更多资源

Functional magnetic resonance imaging (fMRI) is widely viewed as the gold standard for studying brain function due to its high spatial resolution and non-invasive nature. However, it is well established that changes in breathing patterns and heart rate strongly influence the blood oxygen-level dependent (BOLD) fMRI signal and this, in turn, can have considerable effects on fMRI studies, particularly resting-state studies. The dynamic effects of physiological processes are often quantified by using convolution models along with simultaneously recorded physiological data. In this context, physiological response function (PRF) curves (cardiac and respiratory response functions), which are convolved with the corresponding physiological fluctuations, are commonly employed. While it has often been suggested that the PRF curves may be region- or subject-specific, it is still an open question whether this is the case. In the present study, we propose a novel framework for the robust estimation of PRF curves and use this framework to rigorously examine the implications of using population-, subject-, session- and scan-specific PRF curves. The proposed framework was tested on resting-state fMRI and physiological data from the Human Connectome Project. Our results suggest that PRF curves vary significantly across subjects and, to a lesser extent, across sessions from the same subject. These differences can be partly attributed to physiological variables such as the mean and variance of the heart rate during the scan. The proposed methodological framework can be used to obtain robust scan-specific PRF curves from data records with duration longer than 5 min, exhibiting significantly improved performance compared to previously defined canonical cardiac and respiration response functions. Besides removing physiological confounds from the BOLD signal, accurate modeling of subject- (or session-/scan-) specific PRF curves is of importance in studies that involve populations with altered vascular responses, such as aging subjects.

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