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The impact of inspired oxygen levels on calibrated fMRI measurements of M, OEF and resting CMRO2 using combined hypercapnia and hyperoxia
by
Hoge, Richard D.
, Lajoie, Isabelle
, Tancredi, Felipe B.
in
Accuracy
/ Biology and Life Sciences
/ Blood flow
/ Blood pressure
/ Calibration
/ Cerebral blood flow
/ Cerebrovascular Circulation - physiology
/ Error correction
/ Estimates
/ Functional magnetic resonance imaging
/ Gene mapping
/ Humans
/ Hypercapnia
/ Hypercapnia - metabolism
/ Hyperoxia
/ Hyperoxia - metabolism
/ Interpolation
/ Magnetic Resonance Imaging
/ Mapping
/ Medicine and Health Sciences
/ Metabolic rate
/ Metabolism
/ Neurosurgery
/ Nose
/ Oxygen
/ Oxygen - metabolism
/ Oxygen Consumption - physiology
/ Parameters
/ Partial pressure
/ Physical Sciences
/ Research and Analysis Methods
/ Sinus
/ Sinuses
2017
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The impact of inspired oxygen levels on calibrated fMRI measurements of M, OEF and resting CMRO2 using combined hypercapnia and hyperoxia
by
Hoge, Richard D.
, Lajoie, Isabelle
, Tancredi, Felipe B.
in
Accuracy
/ Biology and Life Sciences
/ Blood flow
/ Blood pressure
/ Calibration
/ Cerebral blood flow
/ Cerebrovascular Circulation - physiology
/ Error correction
/ Estimates
/ Functional magnetic resonance imaging
/ Gene mapping
/ Humans
/ Hypercapnia
/ Hypercapnia - metabolism
/ Hyperoxia
/ Hyperoxia - metabolism
/ Interpolation
/ Magnetic Resonance Imaging
/ Mapping
/ Medicine and Health Sciences
/ Metabolic rate
/ Metabolism
/ Neurosurgery
/ Nose
/ Oxygen
/ Oxygen - metabolism
/ Oxygen Consumption - physiology
/ Parameters
/ Partial pressure
/ Physical Sciences
/ Research and Analysis Methods
/ Sinus
/ Sinuses
2017
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The impact of inspired oxygen levels on calibrated fMRI measurements of M, OEF and resting CMRO2 using combined hypercapnia and hyperoxia
by
Hoge, Richard D.
, Lajoie, Isabelle
, Tancredi, Felipe B.
in
Accuracy
/ Biology and Life Sciences
/ Blood flow
/ Blood pressure
/ Calibration
/ Cerebral blood flow
/ Cerebrovascular Circulation - physiology
/ Error correction
/ Estimates
/ Functional magnetic resonance imaging
/ Gene mapping
/ Humans
/ Hypercapnia
/ Hypercapnia - metabolism
/ Hyperoxia
/ Hyperoxia - metabolism
/ Interpolation
/ Magnetic Resonance Imaging
/ Mapping
/ Medicine and Health Sciences
/ Metabolic rate
/ Metabolism
/ Neurosurgery
/ Nose
/ Oxygen
/ Oxygen - metabolism
/ Oxygen Consumption - physiology
/ Parameters
/ Partial pressure
/ Physical Sciences
/ Research and Analysis Methods
/ Sinus
/ Sinuses
2017
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The impact of inspired oxygen levels on calibrated fMRI measurements of M, OEF and resting CMRO2 using combined hypercapnia and hyperoxia
Journal Article
The impact of inspired oxygen levels on calibrated fMRI measurements of M, OEF and resting CMRO2 using combined hypercapnia and hyperoxia
2017
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Overview
Recent calibrated fMRI techniques using combined hypercapnia and hyperoxia allow the mapping of resting cerebral metabolic rate of oxygen (CMRO2) in absolute units, oxygen extraction fraction (OEF) and calibration parameter M (maximum BOLD). The adoption of such technique necessitates knowledge about the precision and accuracy of the model-derived parameters. One of the factors that may impact the precision and accuracy is the level of oxygen provided during periods of hyperoxia (HO). A high level of oxygen may bring the BOLD responses closer to the maximum M value, and hence reduce the error associated with the M interpolation. However, an increased concentration of paramagnetic oxygen in the inhaled air may result in a larger susceptibility area around the frontal sinuses and nasal cavity. Additionally, a higher O2 level may generate a larger arterial blood T1 shortening, which require a bigger cerebral blood flow (CBF) T1 correction. To evaluate the impact of inspired oxygen levels on M, OEF and CMRO2 estimates, a cohort of six healthy adults underwent two different protocols: one where 60% of O2 was administered during HO (low HO or LHO) and one where 100% O2 was administered (high HO or HHO). The QUantitative O2 (QUO2) MRI approach was employed, where CBF and R2* are simultaneously acquired during periods of hypercapnia (HC) and hyperoxia, using a clinical 3 T scanner. Scan sessions were repeated to assess repeatability of results at the different O2 levels. Our T1 values during periods of hyperoxia were estimated based on an empirical ex-vivo relationship between T1 and the arterial partial pressure of O2. As expected, our T1 estimates revealed a larger T1 shortening in arterial blood when administering 100% O2 relative to 60% O2 (T1LHO = 1.56±0.01 sec vs. T1HHO = 1.47±0.01 sec, P < 4*10-13). In regard to the susceptibility artifacts, the patterns and number of affected voxels were comparable irrespective of the O2 concentration. Finally, the model-derived estimates were consistent regardless of the HO levels, indicating that the different effects are adequately accounted for within the model.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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