## Abstract ## Purpose To develop a new method of measuring quantitative regional cerebral blood volume (CBV) using epochs of hyperoxia as an intravenous contrast agent with T2\*βweighted MRI. ## Materials and Methods Images were acquired from six subjects (four male, two female, mean age 29 Β± 3
Measurement of absolute arterial cerebral blood volume in human brain without using a contrast agent
β Scribed by Jun Hua; Qin Qin; James J. Pekar; Peter C. M. van Zijl
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 341 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0952-3480
- DOI
- 10.1002/nbm.1693
No coin nor oath required. For personal study only.
β¦ Synopsis
Arterial cerebral blood volume (CBV a ) is a vital indicator of tissue perfusion and vascular reactivity. We extended the recently developed inflow vascular-space-occupancy (iVASO) MRI technique, which uses spatially selective inversion to suppress the signal from blood flowing into a slice, with a control scan to measure absolute CBV a using cerebrospinal fluid (CSF) for signal normalization. Images were acquired at multiple blood nulling times to account for the heterogeneity of arterial transit times across the brain, from which both CBV a and arterial transit times were quantified. Arteriolar CBV a was determined separately by incorporating velocity-dependent bipolar crusher gradients. Gray matter (GM) CBV a values (n = 11) were 2.04 Β± 0.27 and 0.76 Β± 0.17 ml blood/100 ml tissue without and with crusher gradients (b = 1.8 s/mm 2 ), respectively. Arterial transit times were 671 Β± 43 and 785 Β± 69 ms, respectively. The arterial origin of the signal was validated by measuring its T 2 , which was within the arterial range. The proposed approach does not require exogenous contrast agent administration, and provides a noninvasive alternative to existing blood volume techniques for mapping absolute CBV a in studies of brain physiology and neurovascular diseases.
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