Author: Jingyuan E Chen1, Laura D Lewis2, Catie Chang3, Qiyuan Tian4, Nina E Fultz5, Ned A Ohringer5, Bruce R Rosen6, Jonathan R Polimeni6
Affiliation: <sup>1</sup> Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA; Department of Radiology, Harvard Medical School, Boston, MA, USA. Electronic address: jechen@mgh.harvard.edu.
<sup>2</sup> Department of Biomedical Engineering, Boston University, Boston, MA, USA.
<sup>3</sup> Department of Electrical Engineering and Computer Science, Vanderbilt University, Nashville, TN, USA.
<sup>4</sup> Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA; Department of Radiology, Harvard Medical School, Boston, MA, USA.
<sup>5</sup> Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA.
<sup>6</sup> Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA; Department of Radiology, Harvard Medical School, Boston, MA, USA; Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Cambridge, MA, USA.
Conference/Journal: Neuroimage
Date published: 2020 Jun 1
Other:
Volume ID: 213 , Pages: 116707 , Special Notes: doi: 10.1016/j.neuroimage.2020.116707. , Word Count: 268
Slow changes in systemic brain physiology can elicit large fluctuations in fMRI time series, which manifest as structured spatial patterns of temporal correlations between distant brain regions. Here, we investigated whether such "physiological networks"-sets of segregated brain regions that exhibit similar responses following slow changes in systemic physiology-resemble patterns associated with large-scale networks typically attributed to remotely synchronized neuronal activity. By analyzing a large group of subjects from the 3T Human Connectome Project (HCP) database, we demonstrate brain-wide and noticeably heterogenous dynamics tightly coupled to either respiratory variation or heart rate changes. We show, using synthesized data generated from physiological recordings across subjects, that these physiologically-coupled fluctuations alone can produce networks that strongly resemble previously reported resting-state networks, suggesting that, in some cases, the "physiological networks" seem to mimic the neuronal networks. Further, we show that such physiologically-relevant connectivity estimates appear to dominate the overall connectivity observations in multiple HCP subjects, and that this apparent "physiological connectivity" cannot be removed by the use of a single nuisance regressor for the entire brain (such as global signal regression) due to the clear regional heterogeneity of the physiologically-coupled responses. Our results challenge previous notions that physiological confounds are either localized to large veins or globally coherent across the cortex, therefore emphasizing the necessity to consider potential physiological contributions in fMRI-based functional connectivity studies. The rich spatiotemporal patterns carried by such "physiological" dynamics also suggest great potential for clinical biomarkers that are complementary to large-scale neuronal networks.
Keywords: Global signal regression; Heart rate; Respiratory variation; Resting state functional connectivity; fMRI.
PMID: 32145437 PMCID: PMC7165049 (available on 2021-06-01) DOI: 10.1016/j.neuroimage.2020.116707