EEG spatiospectral patterns and their link to fMRI BOLD signal via variable hemodynamic response functions

2019 ◽  
Vol 318 ◽  
pp. 34-46 ◽  
Author(s):  
René Labounek ◽  
David A. Bridwell ◽  
Radek Mareček ◽  
Martin Lamoš ◽  
Michal Mikl ◽  
...  
2021 ◽  
pp. 0271678X2097858
Author(s):  
Jinxia (Fiona) Yao ◽  
Ho-Ching (Shawn) Yang ◽  
James H Wang ◽  
Zhenhu Liang ◽  
Thomas M Talavage ◽  
...  

Elevated carbon dioxide (CO2) in breathing air is widely used as a vasoactive stimulus to assess cerebrovascular functions under hypercapnia (i.e., “stress test” for the brain). Blood-oxygen-level-dependent (BOLD) is a contrast mechanism used in functional magnetic resonance imaging (fMRI). BOLD is used to study CO2-induced cerebrovascular reactivity (CVR), which is defined as the voxel-wise percentage BOLD signal change per mmHg change in the arterial partial pressure of CO2 (PaCO2). Besides the CVR, two additional important parameters reflecting the cerebrovascular functions are the arrival time of arterial CO2 at each voxel, and the waveform of the local BOLD signal. In this study, we developed a novel analytical method to accurately calculate the arrival time of elevated CO2 at each voxel using the systemic low frequency oscillations (sLFO: 0.01-0.1 Hz) extracted from the CO2 challenge data. In addition, 26 candidate hemodynamic response functions (HRF) were used to quantitatively describe the temporal brain reactions to a CO2 stimulus. We demonstrated that our approach improved the traditional method by allowing us to accurately map three perfusion-related parameters: the relative arrival time of blood, the hemodynamic response function, and CVR during a CO2 challenge.


2010 ◽  
Vol 8 (6) ◽  
pp. 46-46
Author(s):  
P. Bao ◽  
X. Yue ◽  
B. S. Tjan

2021 ◽  
Author(s):  
Kelly Anne Duffy ◽  
Zachary F. Fisher ◽  
Cara A. Arizmendi ◽  
Peter C.M. Molenaar ◽  
Joseph Hopfinger ◽  
...  

2013 ◽  
Vol 27 (2) ◽  
pp. 171-184 ◽  
Author(s):  
Silvia Francesca Storti ◽  
Emanuela Formaggio ◽  
Deborah Moretto ◽  
Alessandra Bertoldo ◽  
Francesca Benedetta Pizzini ◽  
...  

2016 ◽  
Vol 36 (11) ◽  
pp. 1872-1884 ◽  
Author(s):  
Nicholas A Hubbard ◽  
Monroe Turner ◽  
Joanna L Hutchison ◽  
Austin Ouyang ◽  
Jeremy Strain ◽  
...  

Multiple sclerosis (MS) results in inflammatory damage to white matter microstructure. Prior research using blood-oxygen-level dependent (BOLD) imaging indicates MS-related alterations to brain function. What is currently unknown is the extent to which white matter microstructural damage influences BOLD signal in MS. Here we assessed changes in parameters of the BOLD hemodynamic response function (HRF) in patients with relapsing-remitting MS compared to healthy controls. We also used diffusion tensor imaging to assess whether MS-related changes to the BOLD-HRF were affected by changes in white matter microstructural integrity. Our results showed MS-related reductions in BOLD-HRF peak amplitude. These MS-related amplitude decreases were influenced by individual differences in white matter microstructural integrity. Other MS-related factors including altered reaction time, limited spatial extent of BOLD activity, elevated lesion burden, or lesion proximity to regions of interest were not mediators of group differences in BOLD-HRF amplitude. Results are discussed in terms of functional hyperemic mechanisms and implications for analysis of BOLD signal differences.


2014 ◽  
Vol 35 (11) ◽  
pp. 5550-5564 ◽  
Author(s):  
Alexander M. Puckett ◽  
Jedidiah R. Mathis ◽  
Edgar A. DeYoe

2022 ◽  
Vol 9 (03) ◽  
Author(s):  
Tzu-Hao H. Chao ◽  
Wei-Ting Zhang ◽  
Li-Ming Hsu ◽  
Domenic H. Cerri ◽  
Tzu-Wen Wang ◽  
...  

2020 ◽  
Author(s):  
Lindsey J Powell

Although many approaches have been proposed, removing motion artifacts from developmental fNIRS data remains a difficult challenge. In particular, the lack of consistency in motion correction approaches across experimental reports suggests that the field has not yet identified an algorithm that consistently removes the majority of motion contamination while retaining hemodynamic responses, regardless of the idiosyncrasies of particular datasets. Some existing approaches remove the same fraction of variance from each participant’s data; others use participant data to set filtering parameters in ways that result in more stringent thresholds for low-motion participants than high-motion participants. Both types of approach risk leaving artifacts in data from participants with the most motion, while removing signal from participants with the least motion. In contrast, the procedure proposed here identifies and filters motion artifacts on the basis of a fixed, physiologically-justified threshold, so that amount of variance removed is closely associated with the prevalence of motion in each participant’s data. Across multiple contrasts from real experimental datasets, this procedure effectively removes motion artifacts while retaining the hemodynamic response signal, allowing the detection of differential responses to conditions, and recovering canonical hemodynamic response functions for both oxygenated and deoxygenated timecourses, indicated by robust negative correlations between the two hemoglobin types. This motion correction procedure would be appropriate to preregister as a planned component of the preprocessing stream in future fNIRS research.


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