Synopsis
Quantitative MR imaging has the potential to provide information
regarding the biochemical state of tissues and to track biochemical changes
before the onset of morphological changes. However, with current MRI
techniques, it is challenging to obtain signal from tissues with short-T2
relaxation times in the knee, let alone to perform quantitative imaging on
them. Ultrashort echo-time double-echo in steady state (UTEDESS) is a pulse
sequence that offers echo times of 50μs, and high resolution imaging with high SNR
efficiencies. In this study, UTEDESS was also used to measure T2 relaxation
times of the menisci, tendons, and ligaments in human knees. Introduction
MR imaging of connective tissues in the knee such as
the meniscus, ligaments, and tendons is challenging due to their short-T
2
relaxation times. These tissues have been shown to be integral in osteoarthritis
progression [1], which makes it compelling to track their early biochemical
changes before the onset of morphological change. Double-echo in steady state (DESS)
is a 3D pulse sequence that has been used for morphological imaging and T
2 relaxation time measurements
in cartilage [2,3], but the imaging of tissues with short T
2 times is a
challenge. Ultrashort-echo-time DESS (UTEDESS), seen in Fig. 1, is a 3D radial variation
of DESS offering ultrashort echo times, fat-water separation, simultaneous
acquisition of multiple contrast mechanisms, high isotropic resolution, and
excellent SNR efficiency [4]. This study aims to utilize UTEDESS to measure T
2 relaxation
times for the short-T
2 fibrocartilage tissues in the knee, using an improved T
2
fit model.
Methods
The two echoes (S+ and S-) of DESS have been used to
estimate the T2 relaxation times of tissues, assuming relatively high flip
angles [3]. The simple exponential approach in ref. [3] can be improved by
accounting for T1 and the lower flip angles necessary for imaging
short-T2 tissues with short repetition times.
UTEDESS was used to scan 7 healthy volunteers (FOV=16cm,
isotropic resolution=0.63mm, TE/TR=0.4ms/4.8ms, flip angle=10°,
bandwidth=±250kHz, scan time=8:10 minutes, 2x radial undersampling). A Cartesian
DESS sequence (FOV=16cm, resolution=0.63x0.63x3mm, TE/TR=5.1/17.7ms, flip
angle=35°, bandwidth=±31.25kHz, scan time=3:01 minutes) was also used to
calculate T2 in meniscus as a best reference for the UTEDESS T2 maps.
Statistical differences between the two were calculated by a paired Wilcoxon
signed rank test. SNR estimates were calculated using noise from the same
background ROI for both sequences.
T2 maps were generated for manually segmented regions
of the patellar tendon, posterior cruciate ligament (PCL), along with the body,
posterior and anterior horns of the medial and lateral meniscus in single slices.
For the improved T2 fit, T1 for the short-T2 tissues was
approximated at 1s [5] while flip angles of 10° and 35° were used for UTEDESS
and DESS respectively. UTEDESS scans were repeated three times on five
volunteers to assess repeatability and a root-mean-square repeatability coefficient
of variation (rCV) per tissue was calculated.
Results
The T
2 values for the patellar tendon were 9.5±1.5ms (average rCV=2.5%) and
for the PCL were 14.6±1.1ms
(average rCV=2.9%). SNR comparisons amongst UTEDESS and DESS are seen in Fig.
2. Comparisons of the meniscal T
2 values measured with DESS and UTEDESS are
shown in Fig. 3. The repeatability of T
2 measurements with UTEDESS is
seen in the rCV plots in Fig. 4, where the average rCV is 5.1% in the six sub-sections
of the meniscus over three repeated scans. Sample T
2 maps in the lateral
menisci and patellar tendon are shown in Fig. 5.
Discussion
A minimum TE significantly shorter than the expected T2
range is necessary to generate stable and regionally sensitive T2 measurements
in connective tissue [6]. Ideally, a spin-echo sequence would have been used
for validation, but for comparable resolution, it would have a minimum TE=8.5ms.
Cartesian DESS has been demonstrated to offer robust T2 measurements [7], and
offers TE=5.1ms, so it was used as a comparison since it provides higher SNR
than spin-echo in meniscus, which is requisite for accurate T2 exponential
regressions [8]. The background ROI to estimate SNR gave noise estimates
closely matching the noise measured by subtracting two UTEDESS scans, and is
therefore a reasonable comparison metric here.
Despite different scan parameters, the mean meniscal UTEDESS
and DESS T2 relaxation times agreed very well (Fig. 3a), showing no statistical
difference and minimal intra-subject variation (Fig. 3b). The variation of measured
T2 times was minimal over the three repeated scans and the rCV values were
under 10% for all segmented tissues (Fig. 4). However, the meniscal T2 times were
slightly higher than those reported previously [9-11]. Exponential T2 fits can
be overestimated because of biases due to noise, which is an inherent challenge
with short-T2 tissues. Monte-Carlo simulations with UTEDESS showed that
approximately 3ms overestimations are possible due to noise. In addition, magic
angle effects prevalent in the PCL [12] may also have increased the T2 times. In
future work, we plan to characterize the relationship between noise and T2 fits,
as well as to optimize UTEDESS to measure T2 of cartilage.
In conclusion, we have demonstrated rapid T2
relaxation time measurements in connective tissues including meniscus, tendons
and ligaments. Combined with its other features, UTEDESS is a promising whole-joint
method to measure quantitative tissue parameters in short T2 tissues.
Acknowledgements
Research support provided by the NSF DGE-114747, GE
Healthcare, NIH/NIAMS R01 AR063643, NIH/NIAMS K24 AR062068, NIH/NIBIB R01
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