TY - JOUR
T1 - Quantitative phenomenological model of the BOLD contrast mechanism
AU - Dickson, John D.
AU - Ash, Tom W.J.
AU - Williams, Guy B.
AU - Sukstanskii, Alexander L.
AU - Ansorge, Richard E.
AU - Yablonskiy, Dmitriy A.
N1 - Funding Information:
Simulations were run on the Supercomputer of Washington University. We also thank the Engineering and Physical Sciences Research Council and the Medical Research Council (MRC G0600986 WBIC acute brain injury collaborative grant) and NIH Grant R01 NS 055963 (D.A.Y. and A.L.S.) for funding this research.
PY - 2011/9
Y1 - 2011/9
N2 - Different theoretical models of the BOLD contrast mechanism are used for many applications including BOLD quantification (qBOLD) and vessel size imaging, both in health and disease. Each model simplifies the system under consideration, making approximations about the structure of the blood vessel network and diffusion of water molecules through inhomogeneities in the magnetic field created by deoxyhemo-globin-containing blood vessels. In this study, Monte-Carlo methods are used to simulate the BOLD MR signal generated by diffusing water molecules in the presence of long, cylindrical blood vessels. Using these simulations we introduce a new, phenomenological model that is far more accurate over a range of blood oxygenation levels and blood vessel radii than existing models. This model could be used to extract physiological parameters of the blood vessel network from experimental data in BOLD-based experiments. We use our model to establish ranges of validity for the existing analytical models of Yablonskiy and Haacke, Kiselev and Posse, Sukstanskii and Yablonskiy (extended to the case of arbitrary time in the spin echo sequence) and Bauer et al. (extended to the case of randomly oriented cylinders). Although these models are shown to be accurate in the limits of diffusion under which they were derived, none of them is accurate for the whole physiological range of blood vessels radii and blood oxygenation levels. We also show the extent of systematic errors that are introduced due to the approximations of these models when used for BOLD signal quantification.
AB - Different theoretical models of the BOLD contrast mechanism are used for many applications including BOLD quantification (qBOLD) and vessel size imaging, both in health and disease. Each model simplifies the system under consideration, making approximations about the structure of the blood vessel network and diffusion of water molecules through inhomogeneities in the magnetic field created by deoxyhemo-globin-containing blood vessels. In this study, Monte-Carlo methods are used to simulate the BOLD MR signal generated by diffusing water molecules in the presence of long, cylindrical blood vessels. Using these simulations we introduce a new, phenomenological model that is far more accurate over a range of blood oxygenation levels and blood vessel radii than existing models. This model could be used to extract physiological parameters of the blood vessel network from experimental data in BOLD-based experiments. We use our model to establish ranges of validity for the existing analytical models of Yablonskiy and Haacke, Kiselev and Posse, Sukstanskii and Yablonskiy (extended to the case of arbitrary time in the spin echo sequence) and Bauer et al. (extended to the case of randomly oriented cylinders). Although these models are shown to be accurate in the limits of diffusion under which they were derived, none of them is accurate for the whole physiological range of blood vessels radii and blood oxygenation levels. We also show the extent of systematic errors that are introduced due to the approximations of these models when used for BOLD signal quantification.
KW - BOLD fMRI
KW - BOLD modelling
KW - Quantitative BOLD
UR - http://www.scopus.com/inward/record.url?scp=84855363579&partnerID=8YFLogxK
U2 - 10.1016/j.jmr.2011.06.003
DO - 10.1016/j.jmr.2011.06.003
M3 - Article
C2 - 21782488
AN - SCOPUS:84855363579
SN - 1090-7807
VL - 212
SP - 17
EP - 25
JO - Journal of Magnetic Resonance
JF - Journal of Magnetic Resonance
IS - 1
ER -