Regression algorithm correcting for partial volume effects in arterial spin labeling MRI

Partial volume effects (PVE) are a consequence of limited spatial resolution in brain imaging. In arterial spin labeling (ASL) MRI, the problem is exacerbated by the nonlinear dependency of the ASL signal on magnetization contributions from each tissue within an imaged voxel. We have developed an algorithm that corrects for PVE in ASL imaging. The algorithm is based on a model that represents the voxel intensity as a weighted sum of pure tissue contribution, where the weighting coefficients are the tissue's fractional volume in the voxel. Using this algorithm, we were able to estimate cerebral blood flow (CBF) for gray matter (GM) and white matter (WM) independently. The average voxelwise ratio of GM to WM CBF was ∼3.2, in good agreement with reports in the literature. As proof of concept, data from PVE‐corrected method were compared with those from the conventional, PVE‐uncorrected method. As hypothesized, the two yielded similar CBF values for voxels containing >95% GM and differed in proportion with the voxels' heterogeneity. More importantly, the GM CBF assessed with the PVE‐corrected method was independent of the voxels' heterogeneity, implying that estimation of flow was unaffected by PVE. An example of application of this algorithm in motor‐activation data is also given. Magn Reson Med, 2008. © 2008 Wiley‐Liss, Inc.

[1]  Jeff Duyn,et al.  H215O PET validation of steady‐state arterial spin tagging cerebral blood flow measurements in humans , 2000, Magnetic resonance in medicine.

[2]  Alan C. Evans,et al.  A General Statistical Analysis for fMRI Data , 2000, NeuroImage.

[3]  J. Gee,et al.  Alzheimer's Disease And Frontotemporal Dementia Exhibit Distinct Atrophy-Behavior Correlates: , 2003 .

[4]  Roger E. Kirk,et al.  Experimental design: Procedures for the behavioral sciences (3rd ed.). , 1995 .

[5]  Murray Grossman,et al.  Alzheimer's disease and frontotemporal dementia exhibit distinct atrophy-behavior correlates: a computer-assisted imaging study. , 2003, Academic radiology.

[6]  N. Schuff,et al.  Pattern of cerebral hypoperfusion in Alzheimer disease and mild cognitive impairment measured with arterial spin-labeling MR imaging: initial experience. , 2005, Radiology.

[7]  Robert Turner,et al.  Cerebral vascular response to hypercapnia: Determination with perfusion MRI at 1.5 and 3.0 Tesla using a pulsed arterial spin labeling technique , 2006, Journal of magnetic resonance imaging : JMRI.

[8]  Peter C M van Zijl,et al.  An account of the discrepancy between MRI and PET cerebral blood flow measures. A high‐field MRI investigation , 2006, NMR in biomedicine.

[9]  C. Rorden,et al.  Introduction to Functional MRI , 2018, Functional MRI.

[10]  L. Parkes,et al.  Quantification of cerebral perfusion using arterial spin labeling: Two‐compartment models , 2005, Journal of magnetic resonance imaging : JMRI.

[11]  David G Norris,et al.  Improving the amplitude‐modulated control experiment for multislice continuous arterial spin labeling , 2005, Magnetic resonance in medicine.

[12]  Correction of partial volume effects for PET imaging: a comparison study , 2004, IEEE Symposium Conference Record Nuclear Science 2004..

[13]  M. Schnall,et al.  Comparison of quantitative perfusion imaging using arterial spin labeling at 1.5 and 4.0 Tesla , 2002, Magnetic resonance in medicine.

[14]  Yaakov Stern,et al.  Multivariate and Univariate Analysis of Continuous Arterial Spin Labeling Perfusion MRI in Alzheimer's Disease , 2008, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[15]  M. Raichle,et al.  What is the Correct Value for the Brain-Blood Partition Coefficient for Water? , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[16]  P. Tofts,et al.  Normal cerebral perfusion measurements using arterial spin labeling: Reproducibility, stability, and age and gender effects , 2004, Magnetic resonance in medicine.

[17]  M. Bronskill,et al.  Cognitive impairment in dementia: correlations with atrophy and cerebrovascular disease quantified by magnetic resonance imaging. , 2002, Brain and Cognition.

[18]  R. Kauppinen,et al.  Inverse T2 contrast at 1.5 Tesla between gray matter and white matter in the occipital lobe of normal adult human brain , 2001 .

[19]  Louis Sokoloff,et al.  A computationally efficient algorithm for determining regional cerebral blood flow in heterogeneous tissues by positron emission tomography , 2001, IEEE Transactions on Medical Imaging.

[20]  Alan C. Evans,et al.  Positron Emission Tomography Partial Volume Correction: Estimation and Algorithms , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[21]  J. Detre,et al.  Reduced Transit-Time Sensitivity in Noninvasive Magnetic Resonance Imaging of Human Cerebral Blood Flow , 1996, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[22]  R. Kauppinen,et al.  Inverse T(2) contrast at 1.5 Tesla between gray matter and white matter in the occipital lobe of normal adult human brain. , 2001, Magnetic resonance in medicine.

[23]  R. Kirk Experimental Design: Procedures for the Behavioral Sciences , 1970 .

[24]  Yong Du,et al.  Partial volume effect compensation for quantitative brain SPECT imaging , 2005, IEEE Transactions on Medical Imaging.

[25]  Truman R. Brown,et al.  An investigation of statistical power for continuous arterial spin labeling imaging at 1.5 T , 2008, NeuroImage.

[26]  G. Aguirre,et al.  Experimental Design and the Relative Sensitivity of BOLD and Perfusion fMRI , 2002, NeuroImage.

[27]  X. Golay,et al.  Perfusion Imaging Using Arterial Spin Labeling , 2004, Topics in magnetic resonance imaging : TMRI.