Magnetic resonance fingerprinting (MRF) is a useful tool for simultaneously obtaining multiple tissue-specific parameters in an efficient imaging experiment. This technique uses transient state acquisitions with pseudo-random acquisition parameters. However, specific schedules may be better suited for certain parameter ranges or sampling patterns. This work aims to introduce a framework for pulse sequence optimization, including aliasing and noise in our estimates, individually or jointly optimizing for T1 and T2 relaxation times. We demonstrated the schedules created by our algorithm using MRI acquisitions on a healthy volunteer. The design framework could improve the efficiency and accuracy of T1 and T2 acquisitions.
Introduction
New methods based on transient-state imaging, including magnetic resonance fingerprinting1 (MRF), have several advantages as they efficiently sample the MR signal and produce quantitative estimates. Despite several accounts looking into optimising such acquisitions2,3,4,5,6, the choice of the parameters of transient-state sequences remains an open problem as the degrees of freedom to design the sequence are nearly unlimited. Here, we propose a framework to optimise T1 and T2 parameters based on Bayesian optimisation algorithms, including aliasing and noise in our estimates. As a demonstration of our framework, we used it to optimally select the varied sequence parameters in an MR Fingerprinting experiment.Our optimisation method was based on a Bayesian optimisation algorithm (BO)7,9. We performed a simulation of an SSFP MRF8 signal evolutions with the Extended Phase Graph (EPG) formalism12. To work on a realistic dataset, we used the 100th slice of a numerical phantom brain from the Brainweb database11, where we also included under-sampling artefacts by applying forward and backward non-uniform Fourier transform13 for each frame. Complex white Gaussian noise was added to the raw k-space data. The overall errors of the quantitative maps was used as the cost function (l2 norm of the difference between maps), excluding the background values. We first individually optimised T1 and T2 estimations; then, we optimised for the two parameters simultaneously. In the latter case, we used the sum of the overall errors of T1 and T2 maps as a cost function. We considered three ways of generating the function consisting of m excitations for FA or TR sequences, where the schedule length m was one of the input parameters of our optimisation model:
The optimised schedules were evaluated in vivo on the brain of a volunteer, using a GE Hdxt 1.5T scanner equipped with an 8ch receive coil (Milwakee, US).
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