A forward modelling approach for the estimation of oxygen extraction fraction by calibrated fMRI

The measurement of the absolute rate of cerebral metabolic oxygen consumption (CMRO2) is likely to offer a valuable biomarker in many brain diseases and could prove to be important in our understanding of neural function. As such there is significant interest in developing robust MRI techniques that can quantify CMRO2 non-invasively. One potential MRI method for the measurement of CMRO2 is via the combination of fMRI and cerebral blood flow (CBF) data acquired during periods of hypercapnic and hyperoxic challenges. This method is based on the combination of two, previously independent, signal calibration techniques. As such analysis of the data has been approached in a stepwise manner, feeding the results of one calibration experiment into the next. Analysing the data in this manner can result in unstable estimates of the output parameter (CMRO2), due to the propagation of errors along the analysis pipeline. Here we present a forward modelling approach that estimates all the model parameters in a one-step solution. The method is implemented using a regularized non-linear least squares approach to provide a robust and computationally efficient solution. The proposed framework is compared with previous analytical approaches using modelling studies and in vivo acquisitions in healthy volunteers (n=10). The stability of parameter estimates is demonstrated to be superior to previous methods (both in vivo and in simulation). In vivo estimates made with the proposed framework also show better agreement with expected physiological variation, demonstrating a strong negative correlation between baseline CBF and oxygen extraction fraction. It is anticipated that the proposed analysis framework will increase the reliability of absolute CMRO2 measurements made with calibrated BOLD.

[1]  M T Madsen,et al.  A simplified formulation of the gamma variate function , 1992 .

[2]  Claudine Joëlle Gauthier,et al.  Absolute quantification of resting oxygen metabolism and metabolic reactivity during functional activation using QUO2 MRI , 2012, NeuroImage.

[3]  Richard B. Buxton,et al.  An analysis of the use of hyperoxia for measuring venous cerebral blood volume: Comparison of the existing method with a new analysis approach , 2013, NeuroImage.

[4]  Stephen M. Smith,et al.  A global optimisation method for robust affine registration of brain images , 2001, Medical Image Anal..

[5]  Xavier Golay,et al.  Determining the longitudinal relaxation time (T1) of blood at 3.0 Tesla , 2004, Magnetic resonance in medicine.

[6]  Richard B. Buxton,et al.  A theoretical framework for estimating cerebral oxygen metabolism changes using the calibrated-BOLD method: Modeling the effects of blood volume distribution, hematocrit, oxygen extraction fraction, and tissue signal properties on the BOLD signal , 2011, NeuroImage.

[7]  E. Kato,et al.  Cerebral blood flow and oxygen metabolism in senile dementia of Alzheimer's type and vascular dementia with deep white matter changes , 1998, Neuroradiology.

[8]  Martin Reivich,et al.  ARTERIAL PCO2 AND CEREBRAL HEMODYNAMICS. , 1964 .

[9]  Karl Herholz,et al.  Assessment of pathophysiology of stroke by positron emission tomography , 1994, European Journal of Nuclear Medicine.

[10]  G. Bruce Pike,et al.  3681 The Effect of Dissolved Oxygen on Relaxation Rates of Blood Plasma , 2013 .

[11]  Ravi S. Menon,et al.  Functional brain mapping by blood oxygenation level-dependent contrast magnetic resonance imaging. A comparison of signal characteristics with a biophysical model. , 1993, Biophysical journal.

[12]  Adriaan A. Lammertsma,et al.  Positron emission tomography andin vivo measurements of tumour perfusion and oxygen utilisation , 2004, Cancer and Metastasis Reviews.

[13]  G. Glover,et al.  Physiological noise in oxygenation‐sensitive magnetic resonance imaging , 2001, Magnetic resonance in medicine.

[14]  Yulin Ge,et al.  Baseline blood oxygenation modulates response amplitude: Physiologic basis for intersubject variations in functional MRI signals , 2008, Magnetic resonance in medicine.

[15]  J. R. Baker,et al.  The intravascular contribution to fmri signal change: monte carlo modeling and diffusion‐weighted studies in vivo , 1995, Magnetic resonance in medicine.

[16]  M. Raichle,et al.  The Effects of Changes in PaCO2 Cerebral Blood Volume, Blood Flow, and Vascular Mean Transit Time , 1974, Stroke.

[17]  G H Glover,et al.  Simple analytic spiral K‐space algorithm , 1999, Magnetic resonance in medicine.

[18]  Isabelle Lajoie,et al.  A simple breathing circuit allowing precise control of inspiratory gases for experimental respiratory manipulations , 2014, BMC Research Notes.

[19]  G. Crelier,et al.  Investigation of BOLD signal dependence on cerebral blood flow and oxygen consumption: The deoxyhemoglobin dilution model , 1999, Magnetic resonance in medicine.

[20]  Abass Alavi,et al.  PET imaging in the assessment of normal and impaired cognitive function. , 2005, Radiologic clinics of North America.

[21]  Daniel P. Bulte,et al.  MRI measurement of oxygen extraction fraction, mean vessel size and cerebral blood volume using serial hyperoxia and hypercapnia , 2014, NeuroImage.

[22]  Richard G. Wise,et al.  Measurement of OEF and absolute CMRO2: MRI-based methods using interleaved and combined hypercapnia and hyperoxia , 2013, NeuroImage.

[23]  T. L. Davis,et al.  Calibrated functional MRI: mapping the dynamics of oxidative metabolism. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[24]  P. Jezzard,et al.  Quantitative measurement of cerebral physiology using respiratory-calibrated MRI , 2012, NeuroImage.

[25]  M. Reivich,et al.  ARTERIAL PCO2 AND CEREBRAL HEMODYNAMICS. , 1965, The American journal of physiology.

[26]  Weili Lin,et al.  Cerebral venous and arterial blood volumes can be estimated separately in humans using magnetic resonance imaging , 2002, Magnetic resonance in medicine.

[27]  Stephen D. Mayhew,et al.  Dynamic Forcing of End-Tidal Carbon Dioxide and Oxygen Applied to Functional Magnetic Resonance Imaging , 2007, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[28]  D. Yablonskiy,et al.  Quantitative BOLD: Mapping of human cerebral deoxygenated blood volume and oxygen extraction fraction: Default state , 2007, Magnetic resonance in medicine.

[29]  R. Buxton,et al.  Quantitative imaging of perfusion using a single subtraction (QUIPSS and QUIPSS II) , 1998 .

[30]  K Broich,et al.  Positron emission tomography in cerebrovascular disorders. , 1992, Seminars in nuclear medicine.

[31]  Daniel Gallichan,et al.  Bayesian inference of hemodynamic changes in functional arterial spin labeling data , 2006, Magnetic resonance in medicine.

[32]  R. Hoge,et al.  Comparison of Cerebral Vascular Reactivity Measures Obtained Using Breath-Holding and CO2 Inhalation , 2013, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.