Magnetic resonance fingerprinting is a methodology for the quantitative estimation of the relaxation times T1,2. An important challenge is to make estimation robust to inhomogeneities of the main magnetic field B0. Free precession sequences with smoothly varying parameters, such as balanced hybrid-state free precession (bHSFP) sequence, can be optimized for T1,2-encoding performance. Previously, magnetic field deviations were assumed to be determined by a separate experiment. Here we develop a numerically optimized bHSFP sequence that takes into account variations in B0 with the aim of mitigating bias due to B0 inhomogeneities. Our numerical results indicate that this approach yields accurate T1,2 estimates when B0 inhomogeneities are unknown.
Introduction
In magnetic resonance fingerprinting (MRF) [1], the relaxation times T1 and T2 are determined quantitatively by matching the evolution of magnetization signal to a precomputed dictionary of patterns or "fingerprints" of tissues. However, inhomogeneities of the magnetic fields corrupt these estimates, producing for example so-called banding artifacts in the case of sequences with balanced gradient moments [1],[2]. The purpose of this work is to develop a numerically optimized fingerprinting sequence based on the hybrid state framework [2,3] that incorporates B0 estimation and mitigates bias due to B0 inhomogeneities. In particular, the approach succeeds in suppressing banding artifacts.The Cramer-Rao bound [5],[6] is a lower bound on the error of any unbiased estimator of a parameter of interest. It is, therefore, a useful proxy for the sensitivity of the data with respect to the parameter, which can be minimized to optimize the measurements [7],[8],[9]. Here we follow such an approach to search for an efficient balanced hybrid-state free precession (bHSFP) sequence with anti-periodic boundary conditions (defined by $$$r(0)=-r(T_C)$$$, where $$$T_C$$$ is the duration of one cycle of the pulse sequence [2]). We use the relative Cramer-Rao bound ($$$rCRB$$$), normalized by the duration of the experiment, as figure of merit and assume that the signal depends on unknown $$$\Delta B_0$$$ variation parameters (as well as the magnetization and the relaxation times). We optimize an $$$\alpha$$$ pattern using the Broyden-Fletcher-Goldfarb-Shanno algorithm. In the most general approach, one would optimize $$$\phi^{nom}$$$ along with the flip angle pattern. However, we found this approach to show poor convergence behavior. Instead, we implicitly enforce equivalent encoding at all $$$\Delta B_0$$$ offsets (within the limits of the RF-hardware) by sweeping through $$$\gamma\Delta B_0 T_R \in [0, 2\pi]$$$ while repeating the same $$$\alpha$$$ pattern. For consistency with hybrid state conditions [2], the changes in the flip angles in consecutive RF pulses $$$\Delta \alpha$$$ were constrained by
$$| \Delta \alpha | \leq \max \left \{\sin^2 \frac {\alpha}{2} - \frac {5}{2} \left(1 - \sqrt E_2 \right)^2,0 \right \} \label {eq:dalphaconstr} $$
where $$$E_2 = \exp (-T_R/T_2)$$$.
Results and Discussion
The optimized bHSFP sequences exhibit smooth $$$\vartheta$$$ and $$$\alpha$$$ patterns (Figure 1), and the $$$\vartheta$$$ pattern is similar to one found when neglecting field inhomogeneities ($$$\Delta B_0 = 0$$$) [2],[3]. Also when plotting the optimized $$$rCRB$$$ as a function of $$$T_C$$$ (Figure 2), we observe that the optimal duration $$$T_C = 3.8$$$ s is also comparable to the ones found in literature for the idealized case. Lastly, Figure 3 indicates that the sequences optimized for unknown $$$B_0$$$ have similar $$$rCRB$$$ as the sequences optimized for known $$$B_0$$$ variations. (Using the latter sequence in a setting when $$$B_0$$$ variations are unknown would have resulted, however, in a significantly higher $$$rCRB$$$.) Moreover, the horizontal lines disappear in Figure 3, which indicates that $$$T_1$$$ and $$$T_2$$$ can be estimated without banding artifacts.Conclusion and Outlook
Our results indicate that incorporating $$$B_0$$$ variations while designing bHSFP sequences for magnetic resonance fingerprinting is a promising avenue to achieve robust estimates of $$$T_1$$$ and $$$T_2$$$ in the presence of $$$B_0$$$ inhomogeneities. Future work will include validation on phantom and in vivo scans. In addition, we will extend our methodology to account for variations in the RF field $$$B_1$$$.[1] Dan Ma, Vikas Gulani, Nicole Seiberlich, Kecheng Liu, Jeffrey L. Sunshine, Jeffrey L. Duerk, and Mark A. Griswold. Magnetic resonance fingerprinting. Nature, 495(7440):187–192, 2013.
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