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Combined angiography and perfusion using radial imaging and arterial spin labeling with structural contrast

Abstract:
Purpose: To develop a non‐contrast MRI method for the simultaneous acquisition of time‐resolved 3D angiographic, perfusion, and multi‐contrast T1‐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 T1‐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 T1‐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 T1‐weighted contrasts and allowed quantitative T1 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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/mrm.70073

Authors


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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-8258-0659
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-0329-824X
More by this author
Role:
Author
ORCID:
0000-0001-6272-8783


Publisher:
Wiley
Journal:
Magnetic Resonance in Medicine More from this journal
Publication date:
2025-09-15
Acceptance date:
2025-08-22
DOI:
EISSN:
1522-2594
ISSN:
0740-3194


Language:
English
Keywords:
Source identifiers:
3286523
Deposit date:
2025-09-16
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