WALINET: A water and lipid identification convolutional neural network for nuisance signal removal in   1 H $$ {}^1\mathrm{H} $$ MR spectroscopic imaging

IF 3 3区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Magnetic Resonance in Medicine Pub Date : 2024-12-31 DOI:10.1002/mrm.30402
Paul J. Weiser, Georg Langs, Stanislav Motyka, Wolfgang Bogner, Sébastien Courvoisier, Malte Hoffmann, Antoine Klauser, Ovidiu C. Andronesi
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引用次数: 0

Abstract

Purpose

Proton magnetic resonance spectroscopic imaging ( 1 H $$ {}^1\mathrm{H} $$ -MRSI) provides noninvasive spectral-spatial mapping of metabolism. However, long-standing problems in whole-brain 1 H $$ {}^1\mathrm{H} $$ -MRSI are spectral overlap of metabolite peaks with large lipid signal from scalp, and overwhelming water signal that distorts spectra. Fast and effective methods are needed for high-resolution 1 H $$ {}^1\mathrm{H} $$ -MRSI to accurately remove lipid and water signals while preserving the metabolite signal. The potential of supervised neural networks for this task remains unexplored, despite their success for other MRSI processing.

Methods

We introduce a deep learning method based on a modified Y-NET network for water and lipid removal in whole-brain 1 H $$ {}^1\mathrm{H} $$ -MRSI. The WALINET (WAter and LIpid neural NETwork) was compared with conventional methods such as the state-of-the-art lipid L2 regularization and Hankel–Lanczos singular value decomposition (HLSVD) water suppression. Methods were evaluated on simulated models and in vivo whole-brain MRSI using NMRSE, SNR, CRLB, and FWHM metrics.

Results

WALINET is significantly faster and needs 8s for high-resolution whole-brain MRSI, compared with 42min for conventional HLSVD+L2. WALINET suppresses lipid and water in the brain by 25–45 and 34–53-fold, respectively. WALINET has better performance than HLSVD+L2, providing: (1) more lipid removal with 41% lower NRMSE; (2) better metabolite signal preservation with 71% lower NRMSE in simulated data; 155% higher SNR and 50% lower CRLB in in vivo data. Metabolic maps obtained by WALINET in healthy subjects and patients show better gray-/white-matter contrast with more visible structural details.

Conclusions

WALINET has superior performance for nuisance signal removal and metabolite quantification on whole-brain 1 H $$ {}^1\mathrm{H} $$ -MRSI compared with conventional state-of-the-art techniques. This represents a new application of deep learning for MRSI processing, with potential for automated high-throughput workflow.

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WALINET:一种水和脂质识别卷积神经网络去除1 H $$ {}^1\mathrm{H} $$磁共振光谱成像中的干扰信号。
目的:质子磁共振波谱成像(1h $$ {}^1\mathrm{H} $$ -MRSI)提供代谢的无创光谱空间映射。然而,全脑1 H $$ {}^1\mathrm{H} $$ -MRSI长期存在的问题是代谢产物峰的光谱重叠与来自头皮的大脂质信号,以及压倒性的水信号扭曲了光谱。高分辨率1 H $$ {}^1\mathrm{H} $$ -MRSI需要快速有效的方法来准确去除脂质和水信号,同时保留代谢物信号。监督神经网络在这项任务中的潜力仍未被探索,尽管它们在其他核磁共振成像处理中取得了成功。方法:我们引入了一种基于改进的Y-NET网络的深度学习方法,用于全脑1 H $$ {}^1\mathrm{H} $$ -MRSI中水和脂质的去除。将WALINET(水和脂质神经网络)与最先进的脂质L2正则化和Hankel-Lanczos奇异值分解(HLSVD)水抑制等传统方法进行了比较。采用NMRSE、信噪比、CRLB和FWHM指标在模拟模型和活体全脑mri上对方法进行评估。结果:WALINET的速度明显更快,高分辨率全脑mri仅需8秒,而传统的HLSVD+L2仅需42分钟。WALINET对脑内脂质和水分的抑制作用分别为25-45倍和34-53倍。WALINET的性能优于HLSVD+L2,提供:(1)更多的脂质去除% lower NRMSE; (2) better metabolite signal preservation with 71% lower NRMSE in simulated data; 155% higher SNR and 50% lower CRLB in in vivo data. Metabolic maps obtained by WALINET in healthy subjects and patients show better gray-/white-matter contrast with more visible structural details.Conclusions: WALINET has superior performance for nuisance signal removal and metabolite quantification on whole-brain   1 H $$ {}^1\mathrm{H} $$ -MRSI compared with conventional state-of-the-art techniques. This represents a new application of deep learning for MRSI processing, with potential for automated high-throughput workflow.
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来源期刊
CiteScore
6.70
自引率
24.20%
发文量
376
审稿时长
2-4 weeks
期刊介绍: Magnetic Resonance in Medicine (Magn Reson Med) is an international journal devoted to the publication of original investigations concerned with all aspects of the development and use of nuclear magnetic resonance and electron paramagnetic resonance techniques for medical applications. Reports of original investigations in the areas of mathematics, computing, engineering, physics, biophysics, chemistry, biochemistry, and physiology directly relevant to magnetic resonance will be accepted, as well as methodology-oriented clinical studies.
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