Florian Wiesinger1,2, Emil Ljungberg2, Mathias Engström3, Sandeep Kaushik1, Tobias Wood2, Steven Williams2, Gareth Barker2, and Ana Beatriz Solana1
1GE Healthcare, Munich, Germany, 2King’s College London, London, United Kingdom, 3GE Healthcare, Stockholm, Sweden
Synopsis
Here we describe a new framework for 3D, high-resolution
Parameter mapping in a Swift and SilenT manner, termed PSST. The method combines T1 and T2 contrast preparation with
segmented, silent, zero TE (ZTE) image encoding and an analytical signal model. Four canonical schemes are presented and demonstrated
in phantom and in-vivo brain experiments.
Introduction
One major thrust in radiology today is image standardization
with rapidly-acquired, quantitative, multi-contrast information. This is critical for multi-center trials, for
the collection of big data and the use of artificial intelligence in evaluating
the data. In the past few years new quantitative,
multi-parametric MR imaging methods have been presented addressing
this need1-4.
Here we present a new framework for Parameter
mapping in a Swift and Silent manner, termed PSST. The method combines T1 and T2 magnetization
preparation, with segmented 3D, fast and silent Zero TE (ZTE)5,6 image
encoding.Methods
Figure 1 illustrates four example implementations (top) and
corresponding signal evolutions (bottom) for the proposed PSST silent parameter
mapping framework. Magnetization
preparation pulses are indicated by blue (T1 inversion recovery preparation),
and red (T2 preparation) lines. The 3D
silent ZTE image encoding segments5,6 (each containing N=256 center-out radial
spokes), indicated in green, are identically repeated for each segment.
The mean longitudinal magnetization averaged over the nth segment (Mz,n) can be stated as the weighted sum of the longitudinal
magnetization immediately preceding this segment (Mprepz,n) and the ZTE steady-state
longitudinal magnetization (Mz,SS) according to:
$$M_{z,n}=M^{prep}_{z,n}f+M_{z,SS}(1-f) \textrm{, with } f=\frac{\beta(1-\beta^N)}{N(1-\beta)} \textrm{, and } \beta=\cos(\alpha)\exp(-\frac{TR}{T1})$$
$$M_{z,SS}=\frac{M_0(1-E1)}{1-E1\cos(\alpha)}, \textrm{with } E1=exp(-\frac{TR}{T1})$$
For small α<<1rad
and short TR<<T1, Mz,SS can be approximated as:
$$M_{z,SS}=\frac{M_0}{1+\frac{T1 \alpha^2}{2 TR}}$$
Apparently, native ZTE (1st column) with very
small α (i.e. α2*T1/(2*TR)<<1)
provides proton density information (M0), which was used as input
for T1 and T2 fitting in the subsequent schemes. T2zz (2nd column, T2 preparation
followed by two ZTE segments) is the fastest scheme providing PD, T1 and T2 maps
using only two ZTE segments. The T1 information
is extracted in a variable flip angle (VFA) sense via the separately acquired
PD information. T1zzz (3rd
column, T1 inversion recovery followed by three ZTE segments) does not include
a T2 sensitizing mechanism and hence only provides PD and T1. T2zT1zzz (4th column, T2
preparation followed by one ZTE segment followed by T1 inversion recovery
followed by two ZTE segments) is a hybrid of the previous schemes and provides
PD, T1 and T2 information.
Corresponding signal evolutions are plotted for gray
matter (GM), white matter (WM) and cerebrospinal fluid (CSF). The considered PSST schemes demonstrate
stronger signal dispersion for T1 than T2 differences. Accordingly, T2 maps are slightly smoothed by
a Gaussian filter with 0.65 voxels full-width-half-maximum.
The PSST silent parameter mapping framework was implemented on
a GE 3T MR750w scanner using an 8-channel brain coil (GE Healthcare, Chicago,
IL), tested and optimized using a quantitative phantom (Eurospin, UK) and, finally,
demonstrated in healthy volunteer brain scans.
Both T1 and T2 magnetization
preparation modules, are using wide-band, adiabatic RF pulses to improve
robustness against B1 inhomogeneity and off-resonance. Scan parameters are listed in the respective
figure captions. Online image reconstruction
was implemented using the Orchestra SDK (GE Healthcare, Chicago, IL) including 3D
Kaiser-Bessel gridding7 and optional total-generalized-variation (TGV)
regularization8. Quantitative T1 and T2
parameter maps were calculated via least-squares dictionary matching of the M0
normalized signals (i.e. Mt,i/M0) using a precalculated
dictionary containing 500*500 (T1,T2) sampling points. The pre-acquired M0 information
improves the conditioning of the fitting and allows differentiating signals
also based on magnitude differences (vs. cross-correlation based dictionary
matching exploiting shape differences only).Results and Discussion
Figure 2 illustrates in-vivo parameter maps of the four
tested PPST schemes using a high resolution 1mm protocol. Native ZTE (left) provides PD information,
which was then used as prior knowledge for the subsequent schemes. T2zz and T2zT1zzz both provide T1 and T2
information, while T1zzz only captures T1 information.
Figure 3 evaluates accuracy, precision and reproducibility using
a quantitative phantom consisting of 11 tubes of known T1 and T2 relaxation
times. The measured T1 and T2 values appear
slightly biased but highly precise in terms of standard deviation. The T2xx scheme (blue dashed
line) appears significantly different; presumably because of its VFA
nature. After an approximate flip angle
correction (i.e. FA~0.88*FAnominal) obtained T1 and T2 values converge
towards the other schemes. Reproducibility
was tested for T2zT1zz and found excellent (i.e. five repetitions with separate
prescan adjustments in between).
Figure 4 demonstrates sub-millimeter PSST results for T2zT1zzz acquired in 11:13, showing PD, T1 and T2 parameter maps together with derived
synthetic T1-FLAIR and T2-FLAIR images. The acoustic noise was measured inside the magnet bore using a dedicated microphone setup and found to be within 5dB(A) to ambient noise for all tested PSST schemes.Conclusion
The presented PSST method allows parameter
mapping in a swift and silent manner. T1
and T2 signal dispersion is accomplished in a controlled manner via discrete magnetization preparation
pulses and steady-state signal weighting. Four canonical PPST schemes are demonstrated for parameter mapping plus synthetic MR contrast generation at different resolutions.References
- Blystad, I., Warntjes, J. B. M., Smedby, O., Landtblom, A. M., Lundberg, P., & Larsson, E. M. (2012). Synthetic MRI of the brain in a clinical setting. Acta radiologica, 53(10), 1158-1163.
- Kvernby, S., Warntjes, M. J. B., Haraldsson, H., Carlhäll, C. J., Engvall, J., & Ebbers, T. (2014). Simultaneous three-dimensional myocardial T1 and T2 mapping in one breath hold with 3D-QALAS. Journal of Cardiovascular Magnetic Resonance, 16(1), 102.
- Ma, D., Gulani, V., Seiberlich, N., Liu, K., Sunshine, J. L., Duerk, J. L., & Griswold, M. A. (2013). Magnetic resonance fingerprinting. Nature, 495(7440), 187.
- Gómez, P. A., Molina-Romero, M., Buonincontri, G., Menzel, M. I., & Menze, B. H. (2019). Designing contrasts for rapid, simultaneous parameter quantification and flow visualization with quantitative transient-state imaging. Scientific reports, 9(1), 8468.
- Madio, D. P., & Lowe, I. J. (1995). Ultra‐fast imaging using low flip angles and FIDs. Magnetic resonance in medicine, 34(4), 525-529.
- Wiesinger, F., Sacolick, L. I., Menini, A., Kaushik, S. S., Ahn, S., Veit‐Haibach, P., ... & Shanbhag, D. D. (2016). Zero TE MR bone imaging in the head. Magnetic resonance in medicine, 75(1), 107-114.
- Beatty, P. J., Nishimura, D. G., & Pauly, J. M. (2005). Rapid gridding reconstruction with a minimal oversampling ratio. IEEE transactions on medical imaging, 24(6), 799-808.
- Knoll, F., Bredies, K., Pock, T., & Stollberger, R. (2011). Second order total generalized variation (TGV) for MRI. Magnetic resonance in medicine, 65(2), 480-491.