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Thesis

Improving acquisition speed and efficiency of advanced arterial spin labelling MRI

Abstract:

Magnetic resonance imaging (MRI) is a notoriously slow imaging method compared with other imaging modalities, for example computed tomography. It can, however, produce contrasts and attain biophysical information that is unattainable by other methods and is thus a valuable clinical tool.

In recent years, image acquisition times have been reduced through image reconstruction methods that require less data than traditional methods. In this thesis, these kinds of methods are used and extended upon for improved acquisition speed of an MRI method that is particularly slow due to requiring multiple encoded acquisitions to produce a single composite image: arterial spin labelling (ASL).

In conventional ASL, two encodings are used; one with "labelled" blood and one without "labelling", such that subtracting one from the other gives an image of just the blood signal. Angiography can be used to visualise blood flow through the arteries, and perfusion imaging to assess oxygen and nutrient supply to the tissue. Some advanced ASL methods require even more encodings that can be decoded to reveal more information about the cerebral haemodynamics. An example of such an advanced ASL method is vessel-encoded ASL, which allows for generation of separate images of blood originating from different arteries.

In this thesis, modern MRI sampling and reconstruction methods are optimised for vessel-encoded ASL and other ASL variants, with the aim of bringing these modalities towards clinically feasible scan times, which would eventually allow for more information-rich assessments of the cerebrovasculature and the perfusion state of the brain in, for example, patients suffering from stroke, dementia, and arteriovenous malformations.

By careful joint consideration of the multi-dimensional data, the data acquisition, and the reconstruction, very high acceleration factors can be achieved. This is demonstrated, first for vessel-encoded ASL angiography in 2D and 3D, then in similar advanced ASL methods (time-encoded ASL angiography, and combined angiography and perfusion imaging). A new radial sampling scheme is also presented and assessed on ASL angiographic data, that could have impact on imaging methods beyond ASL, in particular other dynamic MRI modalities.

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Division:
MSD
Department:
Clinical Neurosciences
Role:
Author

Contributors

Role:
Supervisor
ORCID:
0000-0001-8258-0659
Role:
Supervisor
ORCID:
0000-0001-6272-8783
Role:
Supervisor
ORCID:
0000-0001-7912-2251
Role:
Examiner
Role:
Examiner


More from this funder
Funder identifier:
http://dx.doi.org/10.13039/501100000266
Funding agency for:
Schauman, SS
Grant:
EP/L016052/1
Programme:
Oxford Nottingham Biomedical Imaging CDT


Type of award:
DPhil
Level of award:
Doctoral
Awarding institution:
University of Oxford

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