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6 - Vascular space occupancy (VASO) imaging of cerebral blood volume

from Section 1 - Techniques

Published online by Cambridge University Press:  05 May 2013

Peter B. Barker
Affiliation:
The Johns Hopkins University School of Medicine
Xavier Golay
Affiliation:
National Hospital for Neurology and Neurosurgery, London
Gregory Zaharchuk
Affiliation:
Stanford University Medical Center
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Summary

Introduction

Apart from dynamic contrast-enhanced (DCE) and dynamic susceptibility contrast (DSC) imaging, assessment of cerebral blood volume (CBV) can also be achieved by taking advantage of differences in intrinsic MR properties between blood and surrounding tissues. In this chapter, Vascular Space Occupancy (VASO) MRI, which utilizes T1 difference between tissue and blood to separate signals from these two compartments, is described. This technique can operate in two different “modes,” one intrinsic, without the use of any exogenous contrast agent and the other following injection of a gadolinium (Gd) chelate. Since the first mode is completely based on intrinsic MR properties of the brain compartments, it can be used in subjects in whom injection of a Gd-based contrast agent might be undesirable or unsafe. For repeated measurements of CBV, the measurement can also be performed at a relatively high temporal resolution (e.g., 6 s) compared with conventional DSC or DCE methods, which require a considerable waiting time for the contrast agent to clear from the bloodstream if repetitive measurements are to be made. However, the first mode can only give relative changes in CBV but cannot be used to estimate absolute CBV. To obtain absolute CBV measurements [1], two VASO scans at pre- and post-injection of Gd-based contrast agent are needed. Compared with the other contrast agent-based methods, the VASO approach should provide higher sensitivity because it maximizes the difference in blood signal pre- and post-Gd. Also it does not require the knowledge of arterial input function, and is relatively insensitive to variations in contrast agent concentrations.

Type
Chapter
Information
Clinical Perfusion MRI
Techniques and Applications
, pp. 89 - 102
Publisher: Cambridge University Press
Print publication year: 2013

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References

Kuppusamy, K, Lin, W, Cizek, GR, Haacke, EM.In vivo regional cerebral blood volume: quantitative assessment with 3D T1-weighted pre- and post-contrast MR imaging. Radiology 1996;201:106–12.CrossRefGoogle Scholar
Lu, H, Golay, X, Pekar, JJ, Van Zijl, PC.Functional magnetic resonance imaging based on changes in vascular space occupancy. Magn Reson Med 2003;50:263–74.CrossRefGoogle ScholarPubMed
Donahue, MJ, Lu, H, Jones, CK et al. Theoretical and experimental investigation of the VASO contrast mechanism. Magn Reson Med 2006;56:1261–73.CrossRefGoogle ScholarPubMed
Scouten, A, Constable, RT.VASO-based calculations of CBV change: accounting for the dynamic CSF volume. Magn Reson Med 2008;59:308–15.CrossRefGoogle ScholarPubMed
Wu, WC, Buxton, RB, Wong, EC.Vascular space occupancy weighted imaging with control of residual blood signal and higher contrast-to-noise ratio. IEEE Trans Med Imaging 2007;26:1319–27.CrossRefGoogle ScholarPubMed
Donahue, MJ, van Laar, PJ, van Zijl, PC, Stevens, RD, Hendrikse, J.Vascular space occupancy (VASO) cerebral blood volume-weighted MRI identifies hemodynamic impairment in patients with carotid artery disease. J Magn Reson Imaging 2009;29:718–24.CrossRefGoogle ScholarPubMed
Hua, J, Donahue, MJ, Zhoo, JM, et al. Magnetization transfer enhanced vascular-space-occupancy (MT-VASO) functional MRI. Magn Reson Med 2009;61:944–51.CrossRefGoogle ScholarPubMed
Glielmi, CB, Schuchard, RA, Hu, XP.Estimating cerebral blood volume with expanded vascular space occupancy slice coverage. Magn Reson Med 2009;61:1193–200.CrossRefGoogle ScholarPubMed
Wu, CW, Liu, HL, Chen, JH, Yang, Y.Effects of CBV, CBF, and blood-brain barrier permeability on accuracy of PASL and VASO measurement. Magn Reson Med 2010;63:601–8.CrossRefGoogle ScholarPubMed
Lu, H, Law, M, Johnson, G, et al. Novel approach to the measurement of absolute cerebral blood volume using vascular-space-occupancy magnetic resonance imaging. Magn Reson Med 2005;54:1403–11.CrossRefGoogle ScholarPubMed
Lu, H, Law, M, Ge, Y, et al. Quantitative measurement of spinal cord blood volume in humans using vascular-space-occupancy MRI. NMR Biomed 2008; 21:226–32.CrossRefGoogle ScholarPubMed
Uh, J, Lewis-Amezcua, K, Varghese, R, Lu, H.On the measurement of absolute cerebral blood volume (CBV) using vascular-space-occupancy (VASO) MRI. Magn Reson Med 2009;61:659–67.CrossRefGoogle ScholarPubMed
Uh, J, Lewis-Amezcua, K, Martin-Cook, K et al. Cerebral blood volume in Alzheimer's disease and correlation with tissue structural integrity. Neurobiol Aging 2010;31:2038–46.CrossRefGoogle ScholarPubMed
Uh, J, Lin, AL, Lee, K et al. Validation of VASO cerebral blood volume measurement with positron emission tomography. Magn Reson Med 2011;65:744–9.CrossRefGoogle ScholarPubMed
Lu, H, Clingman, C, Golay, X, van Zijl, PC.Determining the longitudinal relaxation time (T1) of blood at 3.0 Tesla. Magn Reson Med 2004;52:679–82.CrossRefGoogle ScholarPubMed
Harrison, RV, Harel, N, Panesar, J, Mount, RJ.Blood capillary distribution correlates with hemodynamic-based functional imaging in cerebral cortex. Cereb Cortex 2002;12:225–33.CrossRefGoogle ScholarPubMed
Kuschinsky, W.Regulation of cerebral blood flow: an overview. In: Mraovitch, S, Sercombe, R, editors. Neurophysiological Basis of Cerebral Blood Flow Control: An Introduction. London: Johns Libbey & Company Ltd., 1996; 245–62.Google Scholar
Koenig, SH, Brown, RD, 3rd. Relaxometry of magnetic resonance imaging contrast agents. Magn Reson Annu 1987:263–86.
Donahue, KM, Burstein, D, Manning, WJ, Gray, ML.Studies of Gd-DTPA relaxivity and proton exchange rates in tissue. Magn Reson Med 1994;32:66–76.CrossRefGoogle ScholarPubMed
Ibrahim, MA, Emerson, JF, Cotman, CW.Magnetic resonance imaging relaxation times and gadolinium-DTPA relaxivity values in human cerebrospinal fluid. Invest Radiol 1998;33:153–62.CrossRefGoogle ScholarPubMed
Wendland, MF, Saeed, M, Yu, KK, et al. Inversion recovery EPI of bolus transit in rat myocardium using intravascular and extravascular gadolinium-based MR contrast media: dose effects on peak signal enhancement. Magn Reson Med 1994;32:319–29.CrossRefGoogle ScholarPubMed
Herscovitch, P, Raichle, ME.What is the correct value for the brain–blood partition coefficient for water?J Cereb Blood Flow Metab 1985;5:65–9.CrossRefGoogle Scholar
Donahue, MJ, Hua, J, Pekar, JJ, van Zijl, PC.Effect of inflow of fresh blood on vascular-space-occupancy (VASO) contrast. Magn Reson Med 2009;61:473–80.CrossRefGoogle ScholarPubMed
Lu, H.Magnetization “reset” for non-steady-state blood spins in Vascular-Space-Occupancy (VASO) fMRI. Proc Int Soc Magn Reson Med, Toronto, Canada, 2008;406.Google Scholar
Lu, H, van Zijl, PC, Hendrikse, J, Golay, X.Multiple acquisitions with global inversion cycling (MAGIC): a multislice technique for vascular-space-occupancy dependent fMRI. Magn Reson Med 2004;51:9–15.CrossRefGoogle ScholarPubMed
Scouten, A, Constable, RT.Applications and limitations of whole-brain MAGIC VASO functional imaging. Magn Reson Med 2007;58:306–15.CrossRefGoogle ScholarPubMed
Poser, BA, Norris, DG.3D single-shot VASO using a Maxwell gradient compensated GRASE sequence. Magn Reson Med 2009;62:255–62.CrossRefGoogle ScholarPubMed
Poser, BA, Norris, DG.Application of whole-brain CBV-weighted fMRI to a cognitive stimulation paradigm: robust activation detection in a stroop task experiment using 3D GRASE VASO. Hum Brain Mapp 2011;32:974–81.CrossRefGoogle Scholar
Morris, TW, Ekholm, SE, Prentice, LI.The effects of gadolinium-DTPA and -DOTA on neural tissue metabolism. Invest Radiol 1991;26:1087–90.CrossRefGoogle ScholarPubMed
Lu, H, Golay, X, Pekkar, JJ, van Zijl, PC.Sustained poststimulus elevation in cerebral oxygen utilization after vascular recovery. J Cereb Blood Flow Metab 2004;24:764–70.CrossRefGoogle ScholarPubMed
Jin, T, Kim, SG.Improved cortical-layer specificity of vascular space occupancy fMRI with slab inversion relative to spin-echo BOLD at 9.4 T. Neuroimage 2008;40:59–67.CrossRefGoogle ScholarPubMed
Hua, J, Jones, CK, et al. Vascular-Space-Occupancy (VASO) MRI in human brain at 7T. Proc Int Soc Magn Reson Med, Montreal, Quebec, Canada, 2011; 3604.Google Scholar
Lee, SP, Duong, TQ, Yang, G, Iadecola, C, Kim, SG.Relative changes of cerebral arterial and venous blood volumes during increased cerebral blood flow: implications for BOLD fMRI. Magn Reson Med 2001;45:791–800.CrossRefGoogle ScholarPubMed
Perkio, J, Aronen, HJ, Kangasmäki, A, et al. Evaluation of four postprocessing methods for determination of cerebral blood volume and mean transit time by dynamic susceptibility contrast imaging. Magn Reson Med 2002;47:973–81.CrossRefGoogle ScholarPubMed
van Osch, MJ, Vonken, EJ, Viergever, MA, van der Groud, J, Bakker, CJ.Measuring the arterial input function with gradient echo sequences. Magn Reson Med 2003;49:1067–76.CrossRefGoogle ScholarPubMed
Mandeville, JB, Marota, JJ, Kosofsky, BE, et al. Dynamic functional imaging of relative cerebral blood volume during rat forepaw stimulation. Magn Reson Med 1998;39:615–24.CrossRefGoogle ScholarPubMed
Lu, H, Pollack, E, Young, R, et al. Predicting grade of cerebral glioma using vascular-space occupancy MR imaging. AJNR Am J Neuroradiol 2008;29:373–8.CrossRefGoogle ScholarPubMed
Aronen, HJ, Gazit, IE, Louis, DN, et al. Cerebral blood volume maps of gliomas: comparison with tumor grade and histologic findings. Radiology 1994;191:41–51.CrossRefGoogle ScholarPubMed
Law, M, Yang, S, Wang, H, et al. Glioma grading: sensitivity, specificity, and predictive values of perfusion MR imaging and proton MR spectroscopic imaging compared with conventional MR imaging. AJNR Am J Neuroradiol 2003;24:1989–98.Google ScholarPubMed
Burger, PC.Malignant astrocytic neoplasms: classification, pathologic anatomy, and response to treatment. Semin Oncol 1986;13:16–26.Google ScholarPubMed
Law, M, Yang, S, Babb, JS, et al. Comparison of cerebral blood volume and vascular permeability from dynamic susceptibility contrast-enhanced perfusion MR imaging with glioma grade. AJNR Am J Neuroradiol 2004;25:746–55.Google ScholarPubMed
de la Torre, JC.Is Alzheimer's disease a neurodegenerative or a vascular disorder? Data, dogma, and dialectics. Lancet Neurol 2004;3:184–90.CrossRefGoogle ScholarPubMed
Iadecola, C.Neurovascular regulation in the normal brain and in Alzheimer's disease. Nat Rev Neurosci 2004;5:347–60.CrossRefGoogle ScholarPubMed
Zlokovic, BV.Neurovascular mechanisms of Alzheimer's neurodegeneration. Trends Neurosci 2005;28:202–8.CrossRefGoogle ScholarPubMed
Shen, D, Davatzikos, C.HAMMER: hierarchical attribute matching mechanism for elastic registration. IEEE Trans Med Imaging 2002;21:1421–39.CrossRefGoogle ScholarPubMed
Lu, H, Nagae-Poetscher, LM, Golay, X, et al. Routine clinical brain MRI sequences for use at 3.0 Tesla. J Magn Reson Imaging 2005;22:13–22.CrossRefGoogle ScholarPubMed
Dobre, MC, Ugurbil, K, Marjanska, M.Determination of blood longitudinal relaxation time (T1) at high magnetic field strengths. Magn Reson Imaging 2007;25:733–5.CrossRefGoogle ScholarPubMed
Rooney, WD, Johnson, G, Li, X, et al. Magnetic field and tissue dependencies of human brain longitudinal 1H2O relaxation in vivo. Magn Reson Med 2007;57:308–18.CrossRefGoogle ScholarPubMed

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