Combined Arterial Spin Labeling and Diffusion-Weighted Imaging for Noninvasive Estimation of Capillary Volume Fraction and Permeability-Surface Product in the Human Brain. Issue 1 (January 2013)

• Record Type: Journal Article
• Authors: Hales, Patrick W; Clark, Chris A
• Is Part Of: Journal of cerebral blood flow & metabolism. Volume 33:Issue 1(2013)
• Page Start: 67
• Page End: 75
• Publication Date: 2013-01
• Subjects: arterial spin labeling -- blood–brain barrier -- capillaries -- cerebral blood flow -- diffusion-weighted MRI -- perfusion-weighted MRI; Cerebral circulation -- Periodicals; Brain -- Metabolism -- Periodicals; Brain -- Blood-vessels -- Periodicals; Cerebrovascular disease -- Periodicals; 612.824
• DOI: 10.1038/jcbfm.2012.125
• Languages: English
• ISSNs: 0271-678X

Abstract

A number of two-compartment models have been developed for the analysis of arterial spin labeling (ASL) data, from which both cerebral blood flow ( CBF ) and capillary permeability-surface product ( PS ) can be estimated. To derive values of PS, the volume fraction of the ASL signal arising from the intravascular space ( v bw ) must be known a priori. We examined the use of diffusion-weighted imaging (DWI) and subsequent analysis using the intravoxel incoherent motion model to determine v bw in the human brain. These data were then used in a two-compartment ASL model to estimate PS. Imaging was performed in 10 healthy adult subjects, and repeated in five subjects to test reproducibility. In gray matter (excluding large arteries), mean voxel-wise v bw was 2.3 ± 0.2 mL blood/100 g tissue (all subjects mean ± s.d.), and CBF and PS were 44 ± 5 and 108 ± 2 mL per 100 g per minute, respectively. After spatial smoothing using a 6-mm full width at half maximum Gaussian kernel, the coefficient of repeatability of CBF, v bw and PS were 8 mL per 100 g per minute, 0.4 mL blood/100 g tissue, and 13 mL per 100 g per minute, respectively. Our results show that the combined use of ASL and DWI can provide a new, noninvasive methodology for estimating v bw and PS directly, with reproducibility that is sufficient for clinical use.