Effect of inflow of fresh blood on vascular‐space‐occupancy (VASO) contrast

In vascular‐space‐occupancy (VASO)‐MRI, cerebral blood volume (CBV)‐weighted contrast is generated by applying a nonselective inversion pulse followed by imaging when blood water magnetization is zero. An uncertainty in VASO relates to the completeness of blood water nulling. Specifically, radio frequency (RF) coils produce a finite inversion volume, rendering the possibility of fresh, non‐nulled blood. Here, VASO‐functional MRI (fMRI) was performed for varying inversion volume and TR using body coil RF transmission. For thin inversion volume thickness (δtot < 10 mm), VASO signal changes were positive (ΔS/S = 2.1–2.6%). Signal changes were negative and varied in magnitude for intermediate inversion volumes (δtot = 100–300 mm), yet did not differ significantly (P > 0.05) for δtot > 300 mm. These data suggest that blood water is in steady state for δtot > 300 mm. In this appropriate range, long‐TR VASO data converged to a less negative value (ΔS/S = –1.4% ± 0.2%) than short‐TR data (ΔS/S = –2.2% ± 0.2%), implying that cerebral blood flow or transit‐state effects may influence VASO contrast at short TR. Magn Reson Med 61:473–480, 2009. © 2009 Wiley‐Liss, Inc.

[1]  Peter C M van Zijl,et al.  Theoretical and experimental investigation of the VASO contrast mechanism , 2006, Magnetic resonance in medicine.

[2]  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.

[3]  Richard S. J. Frackowiak,et al.  Cerebral blood flow, blood volume and oxygen utilization. Normal values and effect of age. , 1990, Brain : a journal of neurology.

[4]  Risto A. Kauppinen,et al.  Quantitative assessment of blood flow, blood volume and blood oxygenation effects in functional magnetic resonance imaging , 1998, Nature Medicine.

[5]  B. Rosen,et al.  Evidence of a Cerebrovascular Postarteriole Windkessel with Delayed Compliance , 1999, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[6]  Peter C M van Zijl,et al.  Experimental measurement of extravascular parenchymal BOLD effects and tissue oxygen extraction fractions using multi‐echo VASO fMRI at 1.5 and 3.0 T , 2005, Magnetic resonance in medicine.

[7]  C. Iadecola,et al.  Regulation of the cerebral microcirculation during neural activity: is nitric oxide the missing link? , 1993, Trends in Neurosciences.

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

[9]  Xavier Golay,et al.  Routine clinical brain MRI sequences for use at 3.0 Tesla , 2005, Journal of magnetic resonance imaging : JMRI.

[10]  Tao Jin,et al.  Improved cortical-layer specificity of vascular space occupancy fMRI with slab inversion relative to spin-echo BOLD at 9.4 T , 2008, NeuroImage.

[11]  Daniel Gallichan,et al.  Measuring the Effects of Remifentanil on Cerebral Blood Flow and Arterial Arrival Time Using 3D Grase MRI with Pulsed Arterial Spin Labelling , 2008, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[12]  J. Pekar,et al.  Functional magnetic resonance imaging based on changes in vascular space occupancy , 2003, Magnetic resonance in medicine.

[13]  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.

[14]  D. Tank,et al.  Brain magnetic resonance imaging with contrast dependent on blood oxygenation. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[15]  Stefan K. Piechnik,et al.  Modelling vascular reactivity to investigate the basis of the relationship between cerebral blood volume and flow under CO2 manipulation , 2008, NeuroImage.

[16]  S. Ogawa Brain magnetic resonance imaging with contrast-dependent oxygenation , 1990 .

[17]  W Kuschinsky COUPLING OF BLOOD FLOW AND METABOLISM IN THE BRAIN , 1990, Journal of basic and clinical physiology and pharmacology.

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

[19]  Albert Macovski,et al.  Estimating oxygen saturation of blood in vivo with MR imaging at 1.5 T , 1991 .

[20]  Hanzhang Lu,et al.  Intervoxel Heterogeneity of Event-Related Functional Magnetic Resonance Imaging Responses as a Function of T1 Weighting , 2002, NeuroImage.

[21]  G. Britz,et al.  Regulation of Cerebral Blood Flow , 2011, International journal of vascular medicine.

[22]  Anders M. Dale,et al.  Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation , 2007, NeuroImage.

[23]  D. Attwell,et al.  Bidirectional control of CNS capillary diameter by pericytes , 2006, Nature.

[24]  Peter C M van Zijl,et al.  Oxygenation and hematocrit dependence of transverse relaxation rates of blood at 3T , 2007, Magnetic resonance in medicine.