Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection

Purpose To enable fast reconstruction of quantitative susceptibility maps with total variation penalty and automatic regularization parameter selection. Methods ℓ[subscript 1]-Regularized susceptibility mapping is accelerated by variable splitting, which allows closed-form evaluation of each iter...

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Main Authors: Bilgic, Berkin, Fan, Audrey P., Polimeni, Jonathan R., Cauley, Stephen F., Bianciardi, Marta, Adalsteinsson, Elfar, Setsompop, Kawin, Wald, Lawrence
Other Authors: Harvard University--MIT Division of Health Sciences and Technology
Format: Article
Language:en_US
Published: Wiley Blackwell 2015
Online Access:http://hdl.handle.net/1721.1/99688
https://orcid.org/0000-0002-7637-2914
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author Bilgic, Berkin
Fan, Audrey P.
Polimeni, Jonathan R.
Cauley, Stephen F.
Bianciardi, Marta
Adalsteinsson, Elfar
Setsompop, Kawin
Wald, Lawrence
author2 Harvard University--MIT Division of Health Sciences and Technology
author_facet Harvard University--MIT Division of Health Sciences and Technology
Bilgic, Berkin
Fan, Audrey P.
Polimeni, Jonathan R.
Cauley, Stephen F.
Bianciardi, Marta
Adalsteinsson, Elfar
Setsompop, Kawin
Wald, Lawrence
author_sort Bilgic, Berkin
collection MIT
description Purpose To enable fast reconstruction of quantitative susceptibility maps with total variation penalty and automatic regularization parameter selection. Methods ℓ[subscript 1]-Regularized susceptibility mapping is accelerated by variable splitting, which allows closed-form evaluation of each iteration of the algorithm by soft thresholding and fast Fourier transforms. This fast algorithm also renders automatic regularization parameter estimation practical. A weighting mask derived from the magnitude signal can be incorporated to allow edge-aware regularization. Results Compared with the nonlinear conjugate gradient (CG) solver, the proposed method is 20 times faster. A complete pipeline including Laplacian phase unwrapping, background phase removal with SHARP filtering, and ℓ[subscript 1]-regularized dipole inversion at 0.6 mm isotropic resolution is completed in 1.2 min using MATLAB on a standard workstation compared with 22 min using the CG solver. This fast reconstruction allows estimation of regularization parameters with the L-curve method in 13 min, which would have taken 4 h with the CG algorithm. The proposed method also permits magnitude-weighted regularization, which prevents smoothing across edges identified on the magnitude signal. This more complicated optimization problem is solved 5 times faster than the nonlinear CG approach. Utility of the proposed method is also demonstrated in functional blood oxygen level–dependent susceptibility mapping, where processing of the massive time series dataset would otherwise be prohibitive with the CG solver. Conclusion Online reconstruction of regularized susceptibility maps may become feasible with the proposed dipole inversion.
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spelling mit-1721.1/996882022-10-01T20:54:32Z Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection Bilgic, Berkin Fan, Audrey P. Polimeni, Jonathan R. Cauley, Stephen F. Bianciardi, Marta Adalsteinsson, Elfar Setsompop, Kawin Wald, Lawrence Harvard University--MIT Division of Health Sciences and Technology Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Fan, Audrey P. Adalsteinsson, Elfar Wald, Lawrence Purpose To enable fast reconstruction of quantitative susceptibility maps with total variation penalty and automatic regularization parameter selection. Methods ℓ[subscript 1]-Regularized susceptibility mapping is accelerated by variable splitting, which allows closed-form evaluation of each iteration of the algorithm by soft thresholding and fast Fourier transforms. This fast algorithm also renders automatic regularization parameter estimation practical. A weighting mask derived from the magnitude signal can be incorporated to allow edge-aware regularization. Results Compared with the nonlinear conjugate gradient (CG) solver, the proposed method is 20 times faster. A complete pipeline including Laplacian phase unwrapping, background phase removal with SHARP filtering, and ℓ[subscript 1]-regularized dipole inversion at 0.6 mm isotropic resolution is completed in 1.2 min using MATLAB on a standard workstation compared with 22 min using the CG solver. This fast reconstruction allows estimation of regularization parameters with the L-curve method in 13 min, which would have taken 4 h with the CG algorithm. The proposed method also permits magnitude-weighted regularization, which prevents smoothing across edges identified on the magnitude signal. This more complicated optimization problem is solved 5 times faster than the nonlinear CG approach. Utility of the proposed method is also demonstrated in functional blood oxygen level–dependent susceptibility mapping, where processing of the massive time series dataset would otherwise be prohibitive with the CG solver. Conclusion Online reconstruction of regularized susceptibility maps may become feasible with the proposed dipole inversion. 2015-11-03T18:22:03Z 2015-11-03T18:22:03Z 2013-11 2013-10 Article http://purl.org/eprint/type/JournalArticle 07403194 1522-2594 http://hdl.handle.net/1721.1/99688 Bilgic, Berkin, Audrey P. Fan, Jonathan R. Polimeni, Stephen F. Cauley, Marta Bianciardi, Elfar Adalsteinsson, Lawrence L. Wald, and Kawin Setsompop. “Fast Quantitative Susceptibility Mapping with L1-Regularization and Automatic Parameter Selection.” Magn. Reson. Med. 72, no. 5 (November 20, 2013): 1444–1459. https://orcid.org/0000-0002-7637-2914 en_US http://dx.doi.org/10.1002/mrm.25029 Magnetic Resonance in Medicine Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf Wiley Blackwell PMC
spellingShingle Bilgic, Berkin
Fan, Audrey P.
Polimeni, Jonathan R.
Cauley, Stephen F.
Bianciardi, Marta
Adalsteinsson, Elfar
Setsompop, Kawin
Wald, Lawrence
Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection
title Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection
title_full Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection
title_fullStr Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection
title_full_unstemmed Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection
title_short Fast quantitative susceptibility mapping with L1-regularization and automatic parameter selection
title_sort fast quantitative susceptibility mapping with l1 regularization and automatic parameter selection
url http://hdl.handle.net/1721.1/99688
https://orcid.org/0000-0002-7637-2914
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