An end-to-end AI-based framework for automated discovery of rapid CEST/MT MRI acquisition protocols and molecular parameter quantification (AutoCEST)

Purpose: To develop an automated machine-learning-based method for the discovery of rapid and quantitative chemical exchange saturation transfer (CEST) MR fingerprinting acquisition and reconstruction protocols. Methods: An MR physics-governed AI system was trained to generate optimized acquisition...

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Bibliographic Details
Main Authors: Farrar, C.T (Author), Perlman, O. (Author), Rosen, M.S (Author), Zaiss, M. (Author), Zhu, B. (Author)
Format: Article
Language:English
Published: John Wiley and Sons Inc 2022
Subjects:
Online Access:View Fulltext in Publisher
LEADER 03462nam a2200445Ia 4500
001 10-1002-mrm-29173
008 220420s2022 CNT 000 0 und d
020 |a 07403194 (ISSN) 
245 1 0 |a An end-to-end AI-based framework for automated discovery of rapid CEST/MT MRI acquisition protocols and molecular parameter quantification (AutoCEST) 
260 0 |b John Wiley and Sons Inc  |c 2022 
300 |a 19 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1002/mrm.29173 
520 3 |a Purpose: To develop an automated machine-learning-based method for the discovery of rapid and quantitative chemical exchange saturation transfer (CEST) MR fingerprinting acquisition and reconstruction protocols. Methods: An MR physics-governed AI system was trained to generate optimized acquisition schedules and the corresponding quantitative reconstruction neural network. The system (termed AutoCEST) is composed of a CEST saturation block, a spin dynamics module, and a deep reconstruction network, all differentiable and jointly connected. The method was validated using a variety of chemical exchange phantoms and in vivo mouse brains at 9.4T. Results: The acquisition times for AutoCEST optimized schedules ranged from 35 to 71 s, with a quantitative image reconstruction time of only 29 ms. The resulting exchangeable proton concentration maps for the phantoms were in good agreement with the known solute concentrations for AutoCEST sequences (mean absolute error = 2.42 mM; Pearson’s (Formula presented.), (Formula presented.)), but not for an unoptimized sequence (mean absolute error = 65.19 mM; Pearson’s (Formula presented.), (Formula presented.)). Similarly, improved exchange rate agreement was observed between AutoCEST and quantification of exchange using saturation power (QUESP) methods (mean absolute error: 35.8 Hz, Pearson’s (Formula presented.), (Formula presented.)) compared to an unoptimized schedule and QUESP (mean absolute error = 58.2 Hz; Pearson’s (Formula presented.), (Formula presented.)). The AutoCEST in vivo mouse brain semi-solid proton volume fractions were lower in the cortex (12.77% ± 0.75%) compared to the white matter (19.80% ± 0.50%), as expected. Conclusion: AutoCEST can automatically generate optimized CEST/MT acquisition protocols that can be rapidly reconstructed into quantitative exchange parameter maps. © 2022 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine. 
650 0 4 |a Acquisition protocols 
650 0 4 |a Automated discovery 
650 0 4 |a Chemical exchange saturation transfer 
650 0 4 |a chemical exchange saturation transfer (CEST) 
650 0 4 |a deep learning 
650 0 4 |a End to end 
650 0 4 |a Errors 
650 0 4 |a Image reconstruction 
650 0 4 |a In-vivo 
650 0 4 |a Magnetic resonance 
650 0 4 |a magnetic resonance fingerprinting (MRF) 
650 0 4 |a magnetization transfer (MT) 
650 0 4 |a Mean absolute error 
650 0 4 |a Mouse brain 
650 0 4 |a optimization 
650 0 4 |a Phantoms 
650 0 4 |a Phantoms 
650 0 4 |a Protocol parameters 
650 0 4 |a quantitative imaging 
650 0 4 |a Saturation power 
650 0 4 |a Spin dynamics 
700 1 0 |a Farrar, C.T.  |e author 
700 1 0 |a Perlman, O.  |e author 
700 1 0 |a Rosen, M.S.  |e author 
700 1 0 |a Zaiss, M.  |e author 
700 1 0 |a Zhu, B.  |e author 
773 |t Magnetic Resonance in Medicine