Imaging in the presence of subject motion has been an ongoing challenge for
magnetic resonance imaging (MRI). Motion makes MRI data inconsistent, causing
artifacts in conventional anatomical imaging as well as invalidating diffusion
tensor imaging (DTI) reconstruction. In this thesis some of the important issues
regarding the acquisition and reconstruction of anatomical and DTI imaging of
moving subjects are addressed; methods to achieve high resolution and high signalto-
noise ratio (SNR) volume data are proposed.
An approach has been developed that uses multiple overlapped dynamic single shot
slice by slice imaging combined with retrospective alignment and data fusion to
produce self consistent 3D volume images under subject motion. We term this
method as snapshot MRI with volume reconstruction or SVR. The SVR method
has been performed successfully for brain studies on subjects that cannot stay still,
and in some cases were moving substantially during scanning. For example, awake
neonates, deliberately moved adults and, especially, on fetuses, for which no
conventional high resolution 3D method is currently available. Fine structure of the
in-utero fetal brain is clearly revealed for the first time with substantially improved
SNR. The SVR method has been extended to correct motion artifacts from
conventional multi-slice sequences when the subject drifts in position during data
acquisition.
Besides anatomical imaging, the SVR method has also been further extended to
DTI reconstruction when there is subject motion. This has been validated
successfully from an adult who was deliberately moving and then applied to inutero
fetal brain imaging, which no conventional high resolution 3D method is
currently available. Excellent fetal brain 3D apparent diffusion coefficient (ADC)
maps in high resolution have been achieved for the first time as well as promising
fractional Anisotropy (FA) maps.
Pilot clinical studies using SVR reconstructed data to study fetal brain development
in-utero have been performed. Growth curves for the normally developing fetal
brain have been devised by the quantification of cerebral and cerebellar volumes as
well as some one dimensional measurements. A Verhulst model is proposed to
describe these growth curves, and this approach has achieved a correlation over
0.99 between the fitted model and actual data
