Volume 84, Issue 4 pp. 1724-1733
RAPID COMMUNICATION

Accelerating GluCEST imaging using deep learning for B0 correction

Yiran Li

Yiran Li

Department of Electrical and Computer Engineering, Temple University, Philadelphia, Pennsylvania, USA

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Danfeng Xie

Danfeng Xie

Department of Electrical and Computer Engineering, Temple University, Philadelphia, Pennsylvania, USA

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Abigail Cember

Abigail Cember

Department of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Ravi Prakash Reddy Nanga

Ravi Prakash Reddy Nanga

Department of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Hanlu Yang

Hanlu Yang

Department of Electrical and Computer Engineering, Temple University, Philadelphia, Pennsylvania, USA

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Dushyant Kumar

Dushyant Kumar

Department of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Hari Hariharan

Hari Hariharan

Department of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Li Bai

Li Bai

Department of Electrical and Computer Engineering, Temple University, Philadelphia, Pennsylvania, USA

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John A. Detre

John A. Detre

Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Ravinder Reddy

Ravinder Reddy

Department of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Ze Wang

Corresponding Author

Ze Wang

Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA

Correspondence

Ze Wang, Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Email: [email protected]

Twitter: @zewang79875503

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First published: 17 April 2020
Citations: 31

Abstract

Purpose

Glutamate weighted Chemical Exchange Saturation Transfer (GluCEST) MRI is a noninvasive technique for mapping parenchymal glutamate in the brain. Because of the sensitivity to field (B0) inhomogeneity, the total acquisition time is prolonged due to the repeated image acquisitions at several saturation offset frequencies, which can cause practical issues such as increased sensitivity to patient motions. Because GluCEST signal is derived from the small z-spectrum difference, it often has a low signal-to-noise-ratio (SNR). We proposed a novel deep learning (DL)-based algorithm armed with wide activation neural network blocks to address both issues.

Methods

B0 correction based on reduced saturation offset acquisitions was performed for the positive and negative sides of the z-spectrum separately. For each side, a separate deep residual network was trained to learn the nonlinear mapping from few CEST-weighted images acquired at different ppm values to the one at 3 ppm (where GluCEST peaks) in the same side of the z-spectrum.

Results

All DL-based methods outperformed the “traditional” method visually and quantitatively. The wide activation blocks-based method showed the highest performance in terms of Structural Similarity Index (SSIM) and peak signal-to-noise ratio (PSNR), which were 0.84 and 25dB respectively. SNR increases in regions of interest were over 8dB.

Conclusion

We demonstrated that the new DL-based method can reduce the entire GluCEST imaging time by ˜50% and yield higher SNR than current state-of-the-art.

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