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In vivo demonstration of microscopic anisotropy in the human kidney using multidimensional diffusion MRI

Nery, F; Szczepankiewicz, F; Kerkelä, L; Hall, MG; Kaden, E; Gordon, I; Thomas, DL; (2019) In vivo demonstration of microscopic anisotropy in the human kidney using multidimensional diffusion MRI. Magnetic Resonance in Medicine , 82 (6) pp. 2160-2168. 10.1002/mrm.27869. Green open access

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Abstract

Purpose To demonstrate the feasibility of multidimensional diffusion MRI to probe and quantify microscopic fractional anisotropy (µFA) in human kidneys in vivo. Methods Linear tensor encoded (LTE) and spherical tensor encoded (STE) renal diffusion MRI scans were performed in 10 healthy volunteers. Respiratory triggering and image registration were used to minimize motion artefacts during the acquisition. Kidney cortex–medulla were semi‐automatically segmented based on fractional anisotropy (FA) values. A model‐free analysis of LTE and STE signal dependence on b‐value in the renal cortex and medulla was performed. Subsequently, µFA was estimated using a single‐shell approach. Finally, a comparison of conventional FA and µFA is shown. Results The hallmark effect of µFA (divergence of LTE and STE signal with increasing b‐value) was observed in all subjects. A statistically significant difference between LTE and STE signal was found in the cortex and medulla, starting from b = 750 s/mm2 and b = 500 s/mm2, respectively. This difference was maximal at the highest b‐value sampled (b = 1000 s/mm2) which suggests that relatively high b‐values are required for µFA mapping in the kidney compared to conventional FA. Cortical and medullary µFA were, respectively, 0.53 ± 0.09 and 0.65 ± 0.05, both respectively higher than conventional FA (0.19 ± 0.02 and 0.40 ± 0.02). Conclusion The feasibility of combining LTE and STE diffusion MRI to probe and quantify µFA in human kidneys is demonstrated for the first time. By doing so, we show that novel microstructure information—not accessible by conventional diffusion encoding—can be probed by multidimensional diffusion MRI. We also identify relevant technical limitations that warrant further development of the technique for body MRI.

Type: Article
Title: In vivo demonstration of microscopic anisotropy in the human kidney using multidimensional diffusion MRI
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/mrm.27869
Publisher version: https://doi.org/10.1002/mrm.27869
Language: English
Additional information: This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. https://creativecommons.org/licenses/by-nc/4.0/
Keywords: diffusion, fractional anisotropy, kidney, microscopic anisotropy, spherical tensor encoding, tensor‐valued diffusion encoding
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Brain Repair and Rehabilitation
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Developmental Neurosciences Dept
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science > Dept of Computer Science
URI: https://discovery.ucl.ac.uk/id/eprint/10077101
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