msQSM: Morphology-based self-supervised deep learning for quantitative susceptibility mapping

被引:3
|
作者
He, Junjie [1 ,2 ]
Peng, Yunsong [2 ]
Fu, Bangkang [2 ]
Zhu, Yuemin [3 ]
Wang, Lihui [1 ]
Wang, Rongpin [2 ]
机构
[1] Guizhou Univ, Coll Comp Sci & Technol, Engn Res Ctr Text Comp & Cognit Intelligence, Key Lab Intelligent Med Image Anal & Precise Diag, 2870, Huaxi Ave South, Guiyang 550025, Guizhou, Peoples R China
[2] Guizhou Prov Peoples Hosp, Dept Radiol, Int Exemplary Cooperat Base Precis Imaging Diag &, 83 Zhongshan Dong Rd, Guiyang 550002, Guizhou, Peoples R China
[3] Univ Lyon, CREATIS, IRP Metislab, INSA Lyon,CNRS UMR 5220,Inserm U1294, Lyon, France
基金
中国国家自然科学基金;
关键词
Susceptibility quantitative mapping; Self-supervised learning; Arbitrary resolution; Alzheimer's disease; Parkinson's disease; FIELD INHOMOGENEITY; IRON; COSMOS;
D O I
10.1016/j.neuroimage.2023.120181
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative susceptibility mapping (QSM) has been applied to the measurement of iron deposition and the auxil-iary diagnosis of neurodegenerative disease. There still exists a dipole inversion problem in QSM reconstruction. Recently, deep learning approaches have been proposed to resolve this problem. However, most of these ap-proaches are supervised methods that need pairs of the input phase and ground-truth. It remains a challenge to train a model for all resolutions without using the ground-truth and only using one resolution data. To address this, we proposed a self-supervised QSM deep learning method based on morphology. It consists of a morpho-logical QSM builder to decouple the dependency of the QSM on acquisition resolution, and a morphological loss to reduce artifacts effectively and save training time efficiently. The proposed method can reconstruct arbitrary resolution QSM on both human data and animal data, regardless of whether the resolution is higher or lower than that of the training set. Our method outperforms the previous best unsupervised method with a 3.6% higher peak signal-to-noise ratio, 16.2% lower normalized root mean square error, and 22.1% lower high-frequency error norm. The morphological loss reduces training time by 22.1% with respect to the cycle gradient loss used in the previous unsupervised methods. Experimental results show that the proposed method accurately measures QSM with arbitrary resolutions, and achieves state-of-the-art results among unsupervised deep learning meth-ods. Research on applications in neurodegenerative diseases found that our method is robust enough to measure significant increase in striatal magnetic susceptibility in patients during Alzheimer's disease progression, as well as significant increase in substantia nigra susceptibility in Parkinson's disease patients, and can be used as an auxiliary differential diagnosis tool for Alzheimer's disease and Parkinson's disease.
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页数:12
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