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Hess, A. T.

Publications and source records attributed to Hess, A. T..

2 recordsLinked to original sources

Investigating motion-induced signal corruption in steady-state diffusion MRI

PurposeDiffusion-weighted steady-state free precession (DW-SSFP) is a diffusion imaging sequence achieving high SNR efficiency. A key challenge for in vivo DW-SSFP is the sequences severe motion sensitivity, currently limiting investigations to low or no motion regimes. Here we establish a framework to both (1) model and (2) correct for the impact of subject motion associated with the underlying magnetisation distribution of DW-SSFP. Theory and MethodsAn extended phase graphs (EPG) representation of the 1D DW-SSFP signal was established incorporating a motion operator describing rigid body and pulsatile motion. The representation was validated using Monte Carlo simulations, and subsequently integrated into a data fitting routine for motion estimation and correction. The fitting routine was evaluated using both simulations and a voxelwise correction applied to in vivo experimental 2D low-resolution single-shot timeseries DW-SSFP data acquired in the human brain in three healthy volunteers, with a tensor reconstructed from the motion-corrected experimental DW-SSFP data. ResultsThe proposed EPG-motion framework gives excellent agreement to complementary Monte Carlo simulations, demonstrating that diffusion coefficient estimation is robust over a range of motion and SNR regimes. Tensor estimates from the motion-corrected experimental DW-SSFP data give good visual agreement to complementary diffusion-weighted spin-echo (DW-SE) data acquired in the same subject, considerably reducing orientation-dependent motion-induced biases. ConclusionTemporal information capturing the evolution of the DW-SSFP signal can be used to retrospectively (1) estimate subject motion and (2) reconstruct motion-corrected DW-SSFP data. Open-source software is provided, facilitating future investigations into the impact of subject-motion on DW-SSFP acquisitions.

neuroscience↗

SNR-Efficient Whole-Brain Pseudo-Continuous Arterial Spin Labeling Perfusion Imaging at 7 Tesla

PurposeTo optimize pseudo-continuous arterial spin labeling (PCASL) parameters to maximize SNR efficiency for RF power constrained whole brain perfusion imaging at 7 T. MethodsWe used Bloch simulations of pulsatile laminar flow to optimize the PCASL parameters for maximum SNR efficiency, balancing labeling efficiency and total RF power. The optimization included adjusting the inter-RF pulse spacing (TRPCASL), mean B1+ (B1 ave), slice-selective gradient amplitude (Gmax), and mean gradient amplitude (Gave). In vivo data were acquired from four volunteers at 7 T to validate the optimized parameters. Dynamic B0-shimming and flip angle adjustments were utilized to avoid needing to make the PCASL parameters robust to B0/B1+ variations. ResultsThe optimized PCASL parameters achieved a significant (3.1x) reduction in RF power while maintaining high labeling efficiency. This allowed for longer label durations and minimized deadtime, and resulted in a 126% improvement in SNR efficiency in vivo compared to a previously proposed protocol. Additionally, the static tissue response was improved, reducing the required distance between labeling plane and imaging volume. ConclusionThese optimized PCASL parameters provide a robust and efficient approach for whole brain perfusion imaging at 7 T, with significant improvements in SNR efficiency and reduced SAR burden.

neuroscience↗