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Optimization of quasi-diffusion magnetic resonance imaging for quantitative accuracy and time-efficient acquisition. | LitMetric

Optimization of quasi-diffusion magnetic resonance imaging for quantitative accuracy and time-efficient acquisition.

Magn Reson Med

Neurosciences Research Section, Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom.

Published: December 2022

AI Article Synopsis

  • Quasi-diffusion MRI (QDI) is a new technique that estimates diffusion coefficients and characterizes diffusion signal decay in the brain, focusing on optimizing b-value selection for quick clinical imaging.
  • Research involved testing various multi-b-value datasets and analyzing how changes in maximum b-value and noise affect imaging results in healthy volunteers.
  • The study found that optimizing the number of b-value shells enhanced the accuracy and reliability of QDI measurements, successfully balancing speed and detail for practical brain imaging applications.

Article Abstract

Purpose: Quasi-diffusion MRI (QDI) is a novel quantitative technique based on the continuous time random walk model of diffusion dynamics. QDI provides estimates of the diffusion coefficient, in mm  s and a fractional exponent, , defining the non-Gaussianity of the diffusion signal decay. Here, the b-value selection for rapid clinical acquisition of QDI tensor imaging (QDTI) data is optimized.

Methods: Clinically appropriate QDTI acquisitions were optimized in healthy volunteers with respect to a multi-b-value reference (MbR) dataset comprising 29 diffusion-sensitized images arrayed between and 5000 s mm . The effects of varying maximum b-value ( ), number of b-value shells, and the effects of Rician noise were investigated.

Results: QDTI measures showed dependence, most significantly for in white matter, which monotonically decreased with higher leading to improved tissue contrast. Optimized 2 b-value shell acquisitions showed small systematic differences in QDTI measures relative to MbR values, with overestimation of and underestimation of in white matter, and overestimation of and anisotropies in gray and white matter. Additional shells improved the accuracy, precision, and reliability of QDTI estimates with 3 and 4 shells at  s mm , and 4 b-value shells at  s mm , providing minimal bias in and compared to the MbR.

Conclusion: A highly detailed optimization of non-Gaussian dMRI for in vivo brain imaging was performed. QDI provided robust parameterization of non-Gaussian diffusion signal decay in clinically feasible imaging times with high reliability, accuracy, and precision of QDTI measures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804504PMC
http://dx.doi.org/10.1002/mrm.29420DOI Listing

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