Cargando…
Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping
Quantitative susceptibility mapping (QSM) aims to evaluate the distribution of magnetic susceptibility from magnetic resonance phase measurements by solving the ill-conditioned dipole inversion problem. Removing the artifacts and preserving the anisotropy of tissue susceptibility simultaneously is s...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888664/ https://www.ncbi.nlm.nih.gov/pubmed/35250469 http://dx.doi.org/10.3389/fnins.2022.837721 |
_version_ | 1784661210246938624 |
---|---|
author | He, Junjie Wang, Lihui Cao, Ying Wang, Rongpin Zhu, Yuemin |
author_facet | He, Junjie Wang, Lihui Cao, Ying Wang, Rongpin Zhu, Yuemin |
author_sort | He, Junjie |
collection | PubMed |
description | Quantitative susceptibility mapping (QSM) aims to evaluate the distribution of magnetic susceptibility from magnetic resonance phase measurements by solving the ill-conditioned dipole inversion problem. Removing the artifacts and preserving the anisotropy of tissue susceptibility simultaneously is still a challenge in QSM. To deal with this issue, a novel k-QSM network is proposed to resolve dipole inversion issues in QSM reconstruction. The k-QSM network converts the results obtained by truncated k-space division (TKD) into the Fourier domain as inputs. After passing through several convolutional and residual blocks, the ill-posed signals of TKD are corrected by making the network output close to the calculation of susceptibility through multiple orientation sampling (COSMOS)-labeled QSM. To evaluate the superiority of k-QSM, comparisons with several state-of-the-art methods are performed in terms of QSM artifacts removing, anisotropy preserving, generalization ability, and clinical applications. Compared to existing methods, the k-QSM achieves a 22.31% lower normalized root mean square error, 10.30% higher peak signal-to-noise ratio (PSNR), 33.10% lower high-frequency error norm, and 1.06% higher structural similarity. In addition, the orientation-dependent susceptibility variation obtained by k-QSM is significant, verifying that k-QSM has the ability to preserve susceptibility anisotropy. When the trained models are tested on the dataset from different centers, our k-QSM shows a strong generalization ability with the highest PSNR. Moreover, by comparing the susceptibility maps between healthy controls and drug addicts with different methods, we found the proposed k-QSM is more sensitive to the susceptibility abnormality in the patients. The proposed k-QSM method learns less—only to fix the ill-posed signals of TKD, but infers more—both COSMOS-like and anisotropy-preserving QSM results. Its generalization ability and great sensitivity to susceptibility changes can make it a potential method for distinguishing some diseases. |
format | Online Article Text |
id | pubmed-8888664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88886642022-03-03 Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping He, Junjie Wang, Lihui Cao, Ying Wang, Rongpin Zhu, Yuemin Front Neurosci Neuroscience Quantitative susceptibility mapping (QSM) aims to evaluate the distribution of magnetic susceptibility from magnetic resonance phase measurements by solving the ill-conditioned dipole inversion problem. Removing the artifacts and preserving the anisotropy of tissue susceptibility simultaneously is still a challenge in QSM. To deal with this issue, a novel k-QSM network is proposed to resolve dipole inversion issues in QSM reconstruction. The k-QSM network converts the results obtained by truncated k-space division (TKD) into the Fourier domain as inputs. After passing through several convolutional and residual blocks, the ill-posed signals of TKD are corrected by making the network output close to the calculation of susceptibility through multiple orientation sampling (COSMOS)-labeled QSM. To evaluate the superiority of k-QSM, comparisons with several state-of-the-art methods are performed in terms of QSM artifacts removing, anisotropy preserving, generalization ability, and clinical applications. Compared to existing methods, the k-QSM achieves a 22.31% lower normalized root mean square error, 10.30% higher peak signal-to-noise ratio (PSNR), 33.10% lower high-frequency error norm, and 1.06% higher structural similarity. In addition, the orientation-dependent susceptibility variation obtained by k-QSM is significant, verifying that k-QSM has the ability to preserve susceptibility anisotropy. When the trained models are tested on the dataset from different centers, our k-QSM shows a strong generalization ability with the highest PSNR. Moreover, by comparing the susceptibility maps between healthy controls and drug addicts with different methods, we found the proposed k-QSM is more sensitive to the susceptibility abnormality in the patients. The proposed k-QSM method learns less—only to fix the ill-posed signals of TKD, but infers more—both COSMOS-like and anisotropy-preserving QSM results. Its generalization ability and great sensitivity to susceptibility changes can make it a potential method for distinguishing some diseases. Frontiers Media S.A. 2022-02-16 /pmc/articles/PMC8888664/ /pubmed/35250469 http://dx.doi.org/10.3389/fnins.2022.837721 Text en Copyright © 2022 He, Wang, Cao, Wang and Zhu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience He, Junjie Wang, Lihui Cao, Ying Wang, Rongpin Zhu, Yuemin Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping |
title | Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping |
title_full | Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping |
title_fullStr | Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping |
title_full_unstemmed | Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping |
title_short | Learn Less, Infer More: Learning in the Fourier Domain for Quantitative Susceptibility Mapping |
title_sort | learn less, infer more: learning in the fourier domain for quantitative susceptibility mapping |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888664/ https://www.ncbi.nlm.nih.gov/pubmed/35250469 http://dx.doi.org/10.3389/fnins.2022.837721 |
work_keys_str_mv | AT hejunjie learnlessinfermorelearninginthefourierdomainforquantitativesusceptibilitymapping AT wanglihui learnlessinfermorelearninginthefourierdomainforquantitativesusceptibilitymapping AT caoying learnlessinfermorelearninginthefourierdomainforquantitativesusceptibilitymapping AT wangrongpin learnlessinfermorelearninginthefourierdomainforquantitativesusceptibilitymapping AT zhuyuemin learnlessinfermorelearninginthefourierdomainforquantitativesusceptibilitymapping |