Literature DB >> 31131500

Flexible and efficient optimization of quantitative sequences using automatic differentiation of Bloch simulations.

Philip K Lee1,2, Lauren E Watkins1,3, Timothy I Anderson2, Guido Buonincontri4,5, Brian A Hargreaves1,2,3.   

Abstract

PURPOSE: To investigate a computationally efficient method for optimizing the Cramér-Rao Lower Bound (CRLB) of quantitative sequences without using approximations or an analytical expression of the signal.
METHODS: Automatic differentiation was applied to Bloch simulations and used to optimize several quantitative sequences without the need for approximations or an analytical expression. The results were validated with in vivo measurements and comparisons to prior art. Multi-echo spin echo and DESPO T 1 were used as benchmarks to verify the CRLB implementation. The CRLB of the Magnetic Resonance Fingerprinting (MRF) sequence, which has a complicated analytical formulation, was also optimized using automatic differentiation.
RESULTS: The sequence parameters obtained for multi-echo spin echo and DESPO T 1 matched results obtained using conventional methods. In vivo, MRF scans demonstrate that the CRLB optimization obtained with automatic differentiation can improve performance in presence of white noise. For MRF, the CRLB optimization converges in 1.1 CPU hours for N TR = 400 and has O ( N TR ) asymptotic runtime scaling for the calculation of the CRLB objective and gradient.
CONCLUSIONS: Automatic differentiation can be used to optimize the CRLB of quantitative sequences without using approximations or analytical expressions. For MRF, the runtime is computationally efficient and can be used to investigate confounding factors as well as MRF sequences with a greater number of repetitions.
© 2019 International Society for Magnetic Resonance in Medicine.

Entities:  

Keywords:  Cramér-Rao lower bound; automatic differentiation; magnetic resonance fingerprinting; optimal experiment design; quantitative imaging

Mesh:

Year:  2019        PMID: 31131500      PMCID: PMC8057531          DOI: 10.1002/mrm.27832

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


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