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Abstract Purpose To develop a non‐contrast MRI method for the simultaneous acquisition of time‐resolved 3D angiographic, perfusion, and multi‐contrast T 1 ‐weighted structural brain images in a single 6 min acquisition. Methods The proposed combined angiography and perfusion using radial imaging and arterial spin labeling with structural contrast (CAPRIA+S) pulse sequence uses pseudocontinuous arterial spin labeling to label inflowing blood, an inversion pulse to provide background suppression and T 1 ‐weighted contrast, and a continuous 3D golden ratio spoiled gradient echo readout. Label‐control subtraction isolates the blood signal which can be flexibly reconstructed at high/low spatiotemporal resolution for angiography/perfusion imaging. The mean signal retains the static tissue, allowing T 1 ‐weighted structural images to be reconstructed at different effective TIs. CAPRIA+S was compared with conventional time‐of‐flight angiography, 3D‐gradient and spin echo pseudocontinuous arterial spin labeling perfusion imaging, and MPRAGE structural imaging (10 min total) in healthy volunteers. Results CAPRIA+S gave improved distal vessel visibility and fewer artifacts than time‐of‐flight angiography, while also providing dynamic information, with blood transit time and dispersion maps. CAPRIA+S perfusion images were comparable to 3D‐gradient and spin echo data but without through‐slice blurring or artifacts in inferior brain regions. Comparable quantitative cerebral blood flow maps were produced, with CAPRIA+S being significantly more repeatable. Structural CAPRIA+S images were comparable to MPRAGE but also yielded a range of T 1 ‐weighted contrasts and allowed quantitative T 1 maps to be estimated. Conclusion CAPRIA+S is an efficient single acquisition to provide intrinsically co‐registered quantitative information about brain blood flow and structure that has considerable advantages over conventional methods.

More information Original publication

DOI

10.1002/mrm.70073

Type

Journal article

Publisher

Wiley

Publication Date

2026-02-01T00:00:00+00:00

Volume

95

Pages

787 - 802

Total pages

15