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A novel generalized modeling of modified Look-Locker inversion recovery (MOLLI) signal to allow a shorter breath-hold and accurate T1 mapping
Seonghwan Yee1 and Seonghwan Yee2
1CU Anschutz medical, Aurora, CO, United States, 2Radiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States

Synopsis

A novel generalized modeling method is presented here for the MOLLI signal. When compared with the conventional 3-parameter exponential modeling, this new modeling demonstrates the better accuracy, particularly with the larger T1 values in the case of using enhanced acquisition timing scheme (e.g. 4s(1s)3s(1s)2s). The fact that this novel modeling method does not require full recovery of longitudinal magnetization in successive inversion pulses strongly suggests the possibility of further reducing the total MOLLI scan time to the level a few seconds less than 10 s, which would be much beneficial for those patients who have difficulty in holding the breath.

Introduction

The modified Look-Locker inversion recovery (MOLLI) technique (1,2) is a T1 mapping technique widely used for cardiac applications. Its utility has also been extended to other organs, such as liver. However, when used in the organs (including the heart) sensitive to the respiratory motion, it requires a good breath-hold from patients for the accurate T1 quantification. Although the current total acquisition time of approximately 10~12 s is a reasonable breath-hold period for most patients, further reduction of total acquisition time—even if only a few seconds—would be crucial for some patients including pediatrics. With the current MOLLI signal modeling, the limiting factor for the time reduction is the use of the 3 parameter exponential modeling, which assumes the full recovery of longitudinal magnetization before the next inversion pulse. In this study, a new MOLLI signal modeling method without any restriction on the interval between inversion pulses is presented, and its validity is confirmed by applying it to the phantom-based MOLLI signals acquired with different acquisition timing schemes.

Methods

The conventional MOLLI signal modeling is based on the 3-parameter exponential modeling (Eq. [1] in Fig. 1), and the T1 is determined by the Eq. [2] in Fig. 1 (1,3). Here, $$M0-wave$$ and $$T1-wave$$ are used to represent, respectively, the equilibrium magnetization and T1 under the steady-state acquisition condition. The conventional MOLLI modeling can easily be derived when alpha=beta , as shown in the figure. The new modeling method is developed on a more realistic MOLLI acquisition case that is depicted in Fig. 2, where Eq. [3] shows the new modeling to describe the MOLLI signals acquired with the j-th TI (time after inversion) window after the i-th inversion pulse. With the new modeling, the unknown constants to determine would be 4-parameters (M-wave,T1-wave , alpha, and beta), but could be reduced to 3-parameters if, as conventionally assumed, alpha=beta . MRI measurements were done with a T1 phantom (consisting of 12 vials with different T1 values in the range from 200 ms to 2000 ms) in a clinical 1.5T MRI system (Philips, Netherlands). The MOLLI sequence (TR=1.9ms, TE=0.85ms, ETL=92) was run with a native (5s-3s-3s) or enhanced (4s-1s-3s-1s-2s) timing scheme. The reference T1 values of the phantom were also obtained by repeating an inversion recovery (IR)-based fast spin echo sequence (TR=6s, TE=19ms, ETL=11) while the inversion time was varied from 50ms to 5000ms. MOLLI signals were processed with a MATLAB routine developed according to the conventional modeling and the novel modeling presented here.

Results

The T1 map of the T1 phantom used in this study was automatically generated by the MRI system, and is shown in Fig. 3. The vials were numbered from 1 to 12 in the order of their T1 values. The values of all vials from this map were equivalent to the conventionally obtained T1 values from the author’s MATLAB processing routine. The MOLLI signal changes of all vials for the enhanced timing scheme are shown in Fig. 4(a), where deviations from the traditional IR curve are shown toward the larger T1 vials. An example data set from vial 11 was processed by the conventional curve fitting, in Fig. 4(b), and by the novel 3-parameter curve fitting, in Fig. 4(c). The novel modeling strategy produced accurate T1 result and much better curve fitting. The discrepancy of measured T1 by the conventional MOLLI processing, especially in the case of the enhanced scheme, was much reduced by the new modeling approach, as shown in Fig. 5.

Discussion

As typically seen with the large T1 value in the case of the enhanced timing scheme, the deviations of measured signal from the traditional IR is due to the insufficient recovery before next inversion pulse. The new MOLLI processing strategy does not require full recovery of longitudinal magnetization before each inversion pulse, and any interval between inversion pulses is acceptable. As a result, the generally inserted resting period will be unnecessary. The improved T1 accuracy and MOLLI signal fitting in the case of enhanced timing scheme in this study suggests that the new modeling can be utilized to design a new acquisition timing scheme for a much shorter total acquisition time. Proposing specific shorter acquisition timing schemes will be in the topic of another study.

Conclusion

A new MOLLI signal processing strategy introduced here strongly suggests a possibility to design an improved acquisition timing scheme to further reduce the total MOLLI scan time (e.g. a few seconds less than 10 sec) by further reducing the interval between successive inversion pulses.

Acknowledgements

No acknowledgement found.

References

1. Messroghli DR, Radjenovic A, Kozerke S, Higgins DM, Sivananthan MU, Ridgway JP. Modified Look-Locker inversion recovery (MOLLI) for high-resolution T1 mapping of the heart. Magn Reson Med 2004;52(1):141-146.

2. Kellman P, Hansen MS. T1-mapping in the heart: accuracy and precision. J Cardiovasc Magn Reson 2014;16:2.

3. Deichmann R, Haase A. Quantification of T1 values by SNAPSHOT-FLASH NMR imaging. J Magn Reson 1992;96:608-612.

Figures

The conventional MOLLI signal modeling based on the 3-parameter exponential modeling, Eq. [1], which, when A & B are determined, can produce T1 by Eq. [2]. Here, M0-wave and T1-wave are used to represent, respectively, the equilibrium magnetization and T1 under the steady-state acquisition condition following the inversion of the fully recovered magnetization. Derivations of Eqs. [1] & [2] under the steady-state acquisition condition are shown in this figure.

The real MOLLI acquisition is performed as shown here, having the interval of free T1 recovery between steady-state acquisition windows. This interval is “free” because it is not affected by the application of B1 excitation. When each step in the MOLLI acquisition scheme is carefully solved as illustrated here (the detail is beyond the scope of this abstract), the Eq. [3] can be derived to describe general relationship of the MOLLI signals in the arbitrary inversion routine. Unlike the conventional method, the interval between successive inversion pulses is much flexible.

A T1 map of the T1-phantom used in this study. This map was generated by the MRI scanner automatically at the conclusion of the MOLLI scan. The phantom consisted of 12 vials of different T1 values. The vials were numbered here from 1 to 12 in the order of their T1 values. The T1 values of all vials ranged approximately from 200 ms to 2000 ms. As confirmed later by the author’s own processing software, the scanner-generated T1 map was based on the conventional 3-parameter exponential modeling strategy.

MOLLI signal changes, in (a), acquired from the T1 phantom in the case of using the MOLLI acquisition timing scheme typically utilized in the cardiac T1 mapping after injection of the contrast agent. The curve fitting based on the conventional method is demonstrated in (b). For the same data set, the novel modeling was applied as shown in (c). The plots of the fit curves and the R-square values in (b) & (c) demonstrate the superiority of the novel approach. The accuracy was also better in (c) as the reference T1 for this case was 1794.73 ms.

Comparisons between the conventional and novel modeling approaches for the MOLLI signals. The native and enhanced MOLLI acquisition timing schemes are shown in (a) and (b), respectively. The conventional method produce noticeable errors in the larger T1 values particularly with the enhanced MOLLI acquisition scheme. As shown here, the novel approach can recover the underestimation of the T1 values obtained by the conventional method, particularly in the larger T1 values with the enhanced acquisition scheme.

Proc. Intl. Soc. Mag. Reson. Med. 28 (2020)
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