Qiyong Ai1, Ann D. King1, Huimin Zhang1, and Weitian Chen1
1The Chinese University of Hong Kong, Hong Kong, Hong Kong
Synopsis
T1rho imaging is a new MRI sequence for cancer
evaluation but the repeatability of this sequence in the head and neck region is
unknown. T1rho imaging of the head and neck was performed three times
comprising an initial scan (scan 1) followed by a scan 30 minutes (scan 2) and
14 days (scan 3) later. The repeatability, agreement and variance for the parotid
gland, palatine tonsil and tongue were assessed by comparing scan 1 and 2 and comparing
scan 1 and 3. Results suggested that T1rho imaging
could be a reliable sequence for use in the head and neck.
PURPOSE
The
spin-lattice relaxation time in the rotating frame, known as T1rho, is
sensitive to biological processes associated with alterations in the
macromolecular content of tissues. It does not require the injection of an
intravenous contrast agent. T1rho imaging is therefore a potential new MRI sequence for cancer evaluation. In
the head and neck region it may also have an advantage over diffusion weighted imaging
because there is less distortion
from B0 field inhomogeneities 1,2.
The repeatability of T1rho imaging has been shown
to be reliable in tissues such as the liver and cartilage 3-7. However, T1rho imaging is still a new MRI
sequence in the head and neck and the repeatability for this region is unknown.
The purpose of this study is to evaluate whether quantitative T1rho imaging has
reliable repeatability for studying tissues in the head and neck.MATERIALS AND METHODS
This prospective study was performed with local
institutional board approval and written informed consent was obtained from 10
healthy volunteers (median age: 27 years, range: 24-31 years). T1rho imaging of
the head and neck was performed on a Philips Achieva TX 3.0T
scanner (Philips Healthcare) and was performed three times in all volunteers.
The first two scans (scan 1 and scan 2) were performed with a time interval of
30 minutes and the third scan was performed 14 days after the initial scan
(scan 3). T1rho imaging was performed using adiabatic continuous wave constant
amplitude spin-lock approach [1] followed with a single shot turbo spin echo
acquisition. The imaging parameters were: repetition time/echo time 2500/15 msec; field
of view, 230 mm × 216 mm; resolution, 1.2 mm × 1.2 mm; slice
thickness, 5 mm; number of slices, 9; sensitivity encoding factor, 2; frequency of spin-lock, 400Hz; and time of spin
lock, 0, 10, 30, 55, and 90 msec. At each pixel, the image intensity was fitted to
the relaxation model $$y=A\exp{\left(-\frac{\text{TSL}}{\text{T1rho}}\right)}+B$$ to calculate the T1rho value.Pixels
with extreme T1rho values (< 15 msec or > 200 msec) were excluded.
The
left parotid gland, left palatine tonsil, and the tongue were manually contoured.
The repeatability of the intra-session scans (scan 1 vs scan 2) and inter-session
scans (scan 1 vs scan 3) for parotid gland, palatine tonsil and tongue were
evaluated by using Bland-Altman plot and the limits of agreement calculated. Intra-class
coefficient (ICC), within-subject coefficient of variance (wCV), and repeatability
coefficient (RC) were also calculated to assess the repeatability of T1rho
imaging for each of the three tissues. RESULTS
The
mean ± standard deviation of T1rho values for the normal tissues on the three
scans are shown in Table 1. The Bland-Altman plots, showing differences of
T1rho values between intra and inter sessions for each tissue, are shown in
Figure 1a-f. The ICCs, wCVs and RCs comparing intra-session scan and
inter-session scan for each tissue are shown in Table 2. Intra-session ICCs
were high (0.91 – 0.98) and the wCVs were between 1.55% to 3.92% for all
tissues. Inter-session ICCs remained high (0.86 – 0.90) and wCVs were between
2.10% to 3.30% for all tissues. The greatest T1rho RC for all sessions and all
tissues was 4.45 msec. DISCUSSION
Distribution
of plots in the Bland-Altman graphs indicated T1rho values for normal tissues
in the head and neck were considered to be in agreement and interchangeable for
scans repeated intra-session and inter-session. Furthermore, intra-session T1rho
values in each of the three normal tissues showed good repeatability with excellent
agreements (ICCs > 0.9) and low wCVs (1.55% to 3.92%) with only a slight
reduction in the inter-session repeatability. Our results suggest repeatability
of T1rho imaging in the head and neck may be similar to or better than that in
liver and cartilage [3–7].
Results from this study are encouraging because repeatability of quantitative T1rho
imaging will be important in head and neck cancer research aiming to characterise
tumours, predict treatment response and assess intra-treatment changes.CONCLUSION
T1rho
imaging is a repeatable MRI sequence that can be used in head and neck research.Acknowledgements
No acknowledgement found.References
1. Jiang B,
Chen W. On-resonance and off-resonance continuous wave constant amplitude
spin-lock and T1ρ quantification in the presence of B1 and B0 inhomogeneities.
NMR in Biomedicine 2018;31(7):e3928.
2. Chen W.
Artifacts correction for T1rho imaging with constant amplitude spin-lock.
Journal of Magnetic Resonance 2017;274:13–23.
3. Mosher TJ,
Zhang Z, Reddy R, et al. Knee articular
cartilage damage in osteoarthritis: Analysis of MR image biomarker
reproducibility in ACRIN-PA 4001 multicenter trial. Radiology 2011;258:832–42.
4. Li X, Wyatt C,
Rivoire J, et al. Simultaneous Acquisition of T1ρ
and T2 Quantification in Knee Cartilage: Repeatability and Diurnal Variation.
Journal of Magnetic Resonance Imaging 2014;39:1287–93.
5. Wáng YXJ, Deng
M, Lo GG, et al. Breath-hold black-blood T1rho mapping
improves liver T1rho quantification in healthy volunteers. Acta Radiologica
2018;59:257–65.
6. Nemeth A, Di
Marco L, Boutitie F, et al. Reproducibility of
in vivo magnetic resonance imaging T 1 rho and T 2 relaxation time measurements
of hip cartilage at 3.0T in healthy volunteers. Journal of Magnetic Resonance
Imaging 2018;47:1022–33.
7. Sharafi A, Xia
D, Chang G, et al. Biexponential T1ρ Relaxation Mapping of Human Knee
Cartilage in-vivo at 3T. NMR in Biomedicine 2017;30:e3760.