TY - JOUR
T1 - Partial Fourier techniques in single-shot cross-term spatiotemporal encoded MRI
AU - Zhang, Zhiyong
AU - Frydman, Lucio
N1 - We are grateful to Dr. Sagit Shushan (Wolfson Medical Center) and Edna Furman‐Haran (Weizmann) for assistance in the human scans, and to Dr. Gilad Liberman (Weizmann) for assistance in the coding of the 3T experiments. Z.Z thanks Israel's Council of Higher Education and the Koshland Foundation for partial postdoctoral fellowships. Grant sponsors: Israel Science Foundation grant 795/13; EU through ERC‐2016‐PoC grant 751106; Minerva funding (712277) from the Federal German Ministry for Education and Research; Helen and Martin Kimmel Institute for Magnetic Resonance; and the generosity of the Perlman Family Foundation.
PY - 2018/3
Y1 - 2018/3
N2 - Purpose: Cross-term spatiotemporal encoding (xSPEN) is a single-shot approach with exceptional immunity to field heterogeneities, the images of which faithfully deliver 2D spatial distributions without requiring a priori information or using postacquisition corrections. xSPEN, however, suffers from signal-to-noise ratio penalties due to its non-Fourier nature and due to diffusion losses—especially when seeking high resolution. This study explores partial Fourier transform approaches that, acting along either the readout or the spatiotemporally encoded dimensions, reduce these penalties. Methods: xSPEN uses an orthogonal (e.g., z) gradient to read, in direct space, the low-bandwidth (e.g., y) dimension. This substantially changes the nature of partial Fourier acquisitions vis-à-vis conventional imaging counterparts. A suitable theoretical analysis is derived to implement these procedures, along either the spatiotemporally or readout axes. Results: Partial Fourier single-shot xSPEN images were recorded on preclinical and human scanners. Owing to their reduction in the experiments’ acquisition times, this approach provided substantial sensitivity gains vis-à-vis previous implementations for a given targeted in-plane resolution. The physical origins of these gains are explained. Conclusion: Partial Fourier approaches, particularly when implemented along the low-bandwidth spatiotemporal dimension, provide several-fold sensitivity advantages at minimal costs to the execution and processing of the single-shot experiments. Magn Reson Med 79:1506–1514, 2018.
AB - Purpose: Cross-term spatiotemporal encoding (xSPEN) is a single-shot approach with exceptional immunity to field heterogeneities, the images of which faithfully deliver 2D spatial distributions without requiring a priori information or using postacquisition corrections. xSPEN, however, suffers from signal-to-noise ratio penalties due to its non-Fourier nature and due to diffusion losses—especially when seeking high resolution. This study explores partial Fourier transform approaches that, acting along either the readout or the spatiotemporally encoded dimensions, reduce these penalties. Methods: xSPEN uses an orthogonal (e.g., z) gradient to read, in direct space, the low-bandwidth (e.g., y) dimension. This substantially changes the nature of partial Fourier acquisitions vis-à-vis conventional imaging counterparts. A suitable theoretical analysis is derived to implement these procedures, along either the spatiotemporally or readout axes. Results: Partial Fourier single-shot xSPEN images were recorded on preclinical and human scanners. Owing to their reduction in the experiments’ acquisition times, this approach provided substantial sensitivity gains vis-à-vis previous implementations for a given targeted in-plane resolution. The physical origins of these gains are explained. Conclusion: Partial Fourier approaches, particularly when implemented along the low-bandwidth spatiotemporal dimension, provide several-fold sensitivity advantages at minimal costs to the execution and processing of the single-shot experiments. Magn Reson Med 79:1506–1514, 2018.
U2 - 10.1002/mrm.26824
DO - 10.1002/mrm.26824
M3 - مقالة
SN - 0740-3194
VL - 79
SP - 1506
EP - 1514
JO - Magnetic Resonance in Medicine
JF - Magnetic Resonance in Medicine
IS - 3
ER -