Simultaneous PRFS and T1 quantification using bSSFP for Temperature Monitoring
Mingming Wu1, Matthew Tarasek2, Axel Haase3, and Silke Lechner-Greite4

1IMETUM, Technische Universität München, Garching, Germany, 2GE Global Research, Niskayuna, NY, United States, 3Technische Universität München, Garching, Germany, 4GE Global Research, Garching, Germany

Synopsis

Inversion Recovery prepared bSSFP sequence is used to quantify T1 and PRFS simultaneously based on a phase sensitive bSSFP readout. This technique allows for temperature mapping in both adipose and aqueous tissues at the same time. The feasibility of this method is shown with means of a cooling down experiment of a heterogeneous phantom. B0 drift correction is performed based on neighboring voxels in the fatty tissue.

Purpose

Phase contrast proton resonance frequency shift (PRFS) quantification based on Gradient Echo techniques is the prevailing standard when it comes to MR based temperature monitoring during MR-guided thermal treatments1. In order to quantify temperature changes in adipose tissue, alternative MR properties, such as T1 or T2 relaxation, need to be measured. The presence of a heat applicator like the transducer of a High-Intensity Focused Ultrasound (HIFU) setup, or a radio-frequency (RF) applicator consisting of an array of RF antennas inside the MR scanner usually entails the usage of the body coil, resulting in rather low signal to noise ratio (SNR) values. Balanced steady-state free precession (bSSFP) offers larger SNR values than a Spoiled Gradient Recalled Echo (SPGR) readout. Moreover, inversion recovery (IR) or saturation recovery (SR) prepared bSSFP is widely used for fast T1 mapping2,3,4. In a previous work it has been shown that by choosing an asymmetric relation of echo time (TE) and repetition time (TR) the signal phase becomes sensitive to changes in resonance frequency5. In this work the feasibility and challenges of simultaneous PRFS and T1 mapping using bSSFP are demonstrated with a cooling down experiment of a phantom containing agar and a piece of pork lard.

Methods

The phantom consisted of a piece of pork lard which was put into a glass plunger. A liquid solution of agar (3%) was added to it and solidified thereafter. Two wooden skewers were used for guiding the fluoroptic temperature probes (Luxtron FOT Lab Kit, LumaSense Inc, Santa Clara, CA) (Fig. 1c)).

To investigate both T1 mapping quality and expected phase behavior, Bloch simulations were performed using MATLAB (MathWorks, Natick, MA, USA) (Fig. 2). To retain sufficient effect of the inversion preparation TR should be no longer than 7ms. The shortest possible TE for full k-space sampling was 1.9ms. The frequency shift of 0.009 ppm/°C translates into a shift of 1.2775 Hz/°C at 3 Tesla6. This results in a temperature sensitivity of approximately 0.01 rad/°C in the range of linear phase evolution around the resonance frequency, as shown in the simulation (Fig. 2). MR Imaging was conducted on a GE 3T 750w Scanner (Waukesha, WI, USA). A 12-channel GEM head coil was used during the cooling down experiment. The phantom was placed into a hot water bath before scanning in order to heat up. The phantom was subsequently placed into the scanner such that an axial slice covers both temperature sensors (Fig.1). During cooling down 2D T1 mapping with selective inversion on fat frequency followed by bSSFP readout was done. TE was chosen to be the minimum value for full Fourier sampling, which was 1.9ms for this setting (image resolution 128x96, FOV = 22cm, slice thickness = 4mm, flip angle = 35°). Inversion times were chosen to be 260ms, 310ms, 410ms, 610ms, 860ms and 1210ms. T1 maps were generated using a trust-region curve fitting algorithm implemented in MATLAB (MathWorks, Natick, MA, USA) fitting to the signal equation $$$M(TI_k) = A –B *exp(\frac{-TI_k}{T_1})$$$.

Results

Phase difference calculations were done using the image at the earliest measurement time point, at the hottest temperature, as the reference image. Out of the 6 inversion recovery images the last one (TI=1210ms) was chosen respectively. The phase evolution in a ROI close to the temperature probe (red) does not correspond to the simulated values (blue) for this temperature range (Fig. 3b)). However, it is expected that the well-known B0 drift overlays the temperature induced phase shift. As a correction step, the phase of the pork lard (orange curve in Fig. 3b)) in a small ROI which is close to the agar ROI is traced and subtracted from the phase measured in the agar ROI. The corrected phase curve is now very close to the simulated one (violet curve).

The increase of T1 with temperature correspond to the curve found at 1.5 T7. The T1 values are higher, as expected at 3 T. The mean value inside the ROI (Fig. 4a)) depending on the measured temperature is plotted in Fig. 4b).

Discussion

A rather homogeneous B0 field within the image is assumed in order to be located in the step-by-step linear phase curve. The presence of heat applicators, like ultrasound transducer or RF antennas, introduces B0 inhomogeneity, which will introduce banding artifacts. Phase cycled bSSFP acquisition is a solution in order to overcome these artifacts. In this way, the non-linear phase regions will be covered by a linear curve in the second image.

Conclusion

IR prepared bSSFP is able to resolve PRFS phenomenon, thus enabling temperature quantification in both adipose and aqueous tissues at the same time.

Acknowledgements

This project is part of the BERTI program. BERTI is funded by the European Commission under Grant Agreement Number 605162.

References

1. Gellermann J. et al. Noninvasive Magnetic Resonance Thermography of Soft Tissue Sarcomas During Regional Hyperthermia. Cancer 2006, 107 (6): 1373-1382.

2. Scheffler K. et al. T1 Quantification With Inversion Recovery TrueFISP. MRM 2001, 45:720-723

3. Messroghli D. et al. Modified Look-Locker Inversion Recovery (MOLLI) for High-Resolution T1 Mapping of the Heart. MRM 2004, 52:141-146

4. Chow K. et al. Saturation Recovery Single-Shot Acquisition (SASHA) for Myocardial T1 Mapping. MRM 2014, 71:2082-2095

5. Wu M. et al. Towards accurate temperature mapping in adipose tissue with joint T1 and PRFS using Balanced SSFP. Proc. Intl. Soc. Mag. Reson. Med. 23 (2015) 1653

6. McDannold N. Int J Hyperthermia 2005;21:533–546.

7. Baron P. et al. Measurement of the T1 and T2 temperature dependence of human breast adipose tissue. Proc. Intl. Soc. Mag. Reson. Med. 19 (2011)

Figures

Fig. 1: Axial view of phantom. a) Agar compartment, b) pork lard and c) fluoroptic temprature sensor placement.

Fig. 2: Phase dependency on frequency offset for TE = 1.9ms, flip angle = 35°, T1 = 300ms, T2 = 50ms. Blue arrow indicates fat resonance frequency in relation to water at 3 Tesla.

Fig. 3: a) Region of interest (ROI1): 6 pixels in agar next to temperature probe, ROI2: 6 pixels in fat close to ROI1. b) Blue: expected simulated phase, red: measured phase in agar, orange: measured phase in lard, violet: corrected phase for ROI1 by subtracting phase in ROI2, which represents B0 drift.

Fig. 4: a) ROI in lard for T1 calculation. b) Mean T1 value in ROI around temperature probe inside pork lard depending on measured temperature.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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