TY - JOUR
T1 - The effect of gradient nonlinearities on fiber orientation estimates from spherical deconvolution of diffusion magnetic resonance imaging data
AU - Guo, Fenghua
AU - de Luca, Alberto
AU - Parker, Greg
AU - Jones, Derek K
AU - Viergever, Max A
AU - Leemans, Alexander
AU - Tax, Chantal M W
N1 - Funding Information:
China Scholarship Council; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; NIH Institutes and Centers; Wolfson Foundation; EPSRC, Grant/Award Number: EP/M029778/1; Wellcome Trust Strategic Award, Grant/Award Number: 104943/Z/14/Z; Wellcome Trust Investigator Award, Grant/Award Number: 096646/Z/11/Z; Sir Henry Wellcome Fellowship, Grant/Award Number: 215944/Z/19/Z; Dutch Research Council; Veni, Grant/Award Number: 17331; Rubicon, Grant/Award Number: 680‐50‐1527 Funding information
Funding Information:
The research of F. G was supported by China Scholarship Council (CSC). The research of A. L was supported by VIDI Grant 639.072.411 from the Netherlands Organization for Scientific Research (NWO). C. M. W. T. was supported by a Rubicon grant (680-50-1527) and a Veni grant (17331) from the Dutch Research Council (NWO), and a Sir Henry Wellcome Fellowship (215944/Z/19/Z). D. K. J. and C. M. W. T. were supported by a Wellcome Trust Investigator Award (096646/Z/11/Z), and D. K. J. by a Wellcome Trust Strategic Award (104943/Z/14/Z). Part of the Data were acquired at the UK National Facility for in vivo MR Imaging of Human Tissue Microstructure located in CUBRIC funded by the EPSRC (grant EP/M029778/1), and the Wolfson Foundation. The authors acknowledge the 2017 and 2018 MICCAI Computational Diffusion MRI committees (Francesco Grussu, Enrico Kaden, Lipeng Ning, Jelle Veraart, Elisenda Bonet-Carne, and Farshid Sepehrband) and CUBRIC, Cardiff University (Derek Jones, Umesh Rudrapatna, John Evans, Greg Parker, Slawomir Kusmia, Cyril Charron, and David Linden). Part of the data were provided by the Human Connectome Project, WU-Minn Consortium (principal investigators: David van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University.
Funding Information:
The research of F. G was supported by China Scholarship Council (CSC). The research of A. L was supported by VIDI Grant 639.072.411 from the Netherlands Organization for Scientific Research (NWO). C. M. W. T. was supported by a Rubicon grant (680‐50‐1527) and a Veni grant (17331) from the Dutch Research Council (NWO), and a Sir Henry Wellcome Fellowship (215944/Z/19/Z). D. K. J. and C. M. W. T. were supported by a Wellcome Trust Investigator Award (096646/Z/11/Z), and D. K. J. by a Wellcome Trust Strategic Award (104943/Z/14/Z). Part of the Data were acquired at the UK National Facility for in vivo MR Imaging of Human Tissue Microstructure located in CUBRIC funded by the EPSRC (grant EP/M029778/1), and the Wolfson Foundation. The authors acknowledge the 2017 and 2018 MICCAI Computational Diffusion MRI committees (Francesco Grussu, Enrico Kaden, Lipeng Ning, Jelle Veraart, Elisenda Bonet‐Carne, and Farshid Sepehrband) and CUBRIC, Cardiff University (Derek Jones, Umesh Rudrapatna, John Evans, Greg Parker, Slawomir Kusmia, Cyril Charron, and David Linden). Part of the data were provided by the Human Connectome Project, WU‐Minn Consortium (principal investigators: David van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University.
Publisher Copyright:
© 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
PY - 2021/2/1
Y1 - 2021/2/1
N2 - Gradient nonlinearities in magnetic resonance imaging (MRI) cause spatially varying mismatches between the imposed and the effective gradients and can cause significant biases in rotationally invariant diffusion MRI measures derived from, for example, diffusion tensor imaging. The estimation of the orientational organization of fibrous tissue, which is nowadays frequently performed with spherical deconvolution techniques ideally using higher diffusion weightings, can likewise be biased by gradient nonlinearities. We explore the sensitivity of two established spherical deconvolution approaches to gradient nonlinearities, namely constrained spherical deconvolution (CSD) and damped Richardson-Lucy (dRL). Additionally, we propose an extension of dRL to take into account gradient imperfections, without the need of data interpolation. Simulations show that using the effective b-matrix can improve dRL fiber orientation estimation and reduces angular deviations, while CSD can be more robust to gradient nonlinearity depending on the implementation. Angular errors depend on a complex interplay of many factors, including the direction and magnitude of gradient deviations, underlying microstructure, SNR, anisotropy of the effective response function, and diffusion weighting. Notably, angular deviations can also be observed at lower b-values in contrast to the perhaps common assumption that only high b-value data are affected. In in vivo Human Connectome Project data and acquisitions from an ultrastrong gradient (300 mT/m) scanner, angular differences are observed between applying and not applying the effective gradients in dRL estimation. As even small angular differences can lead to error propagation during tractography and as such impact connectivity analyses, incorporating gradient deviations into the estimation of fiber orientations should make such analyses more reliable.
AB - Gradient nonlinearities in magnetic resonance imaging (MRI) cause spatially varying mismatches between the imposed and the effective gradients and can cause significant biases in rotationally invariant diffusion MRI measures derived from, for example, diffusion tensor imaging. The estimation of the orientational organization of fibrous tissue, which is nowadays frequently performed with spherical deconvolution techniques ideally using higher diffusion weightings, can likewise be biased by gradient nonlinearities. We explore the sensitivity of two established spherical deconvolution approaches to gradient nonlinearities, namely constrained spherical deconvolution (CSD) and damped Richardson-Lucy (dRL). Additionally, we propose an extension of dRL to take into account gradient imperfections, without the need of data interpolation. Simulations show that using the effective b-matrix can improve dRL fiber orientation estimation and reduces angular deviations, while CSD can be more robust to gradient nonlinearity depending on the implementation. Angular errors depend on a complex interplay of many factors, including the direction and magnitude of gradient deviations, underlying microstructure, SNR, anisotropy of the effective response function, and diffusion weighting. Notably, angular deviations can also be observed at lower b-values in contrast to the perhaps common assumption that only high b-value data are affected. In in vivo Human Connectome Project data and acquisitions from an ultrastrong gradient (300 mT/m) scanner, angular differences are observed between applying and not applying the effective gradients in dRL estimation. As even small angular differences can lead to error propagation during tractography and as such impact connectivity analyses, incorporating gradient deviations into the estimation of fiber orientations should make such analyses more reliable.
KW - connectivity matrices
KW - constrained spherical deconvolution
KW - damped Richardson-Lucy
KW - diffusion MRI
KW - fiber orientation distribution
KW - gradient nonlinearity
KW - spherical deconvolution
UR - http://www.scopus.com/inward/record.url?scp=85092196263&partnerID=8YFLogxK
U2 - 10.1002/hbm.25228
DO - 10.1002/hbm.25228
M3 - Article
C2 - 33035372
SN - 1065-9471
VL - 42
SP - 367
EP - 383
JO - Human Brain Mapping
JF - Human Brain Mapping
IS - 2
ER -