Jithsa R. Monte1, Melissa T. Hooijmans1, Martijn Froeling2, Jos Oudeman2, Johannes L. Tol1, Mario Maas1, Gustav J. Strijkers1, and Aart J. Nederveen1
1Radiology & Nuclear Medicine, Academic Medical Center, Amsterdam, Netherlands, 2University Medical Center Utrecht, Utrecht, Netherlands
Synopsis
Muscle
injuries are diagnosed using T2-weighted scans, but these techniques lack
specificity for assessing tissue repair. DTI seems more suitable for this
purpose, but reproducibility data is lacking. Therefore, the aim of this study
was to determine the reproducibility of DTI, expressed as the within subject CV
per DTI parameter in the hamstrings of healthy athletes.
The wsCV
values reported here for DTI parameters are superior or similar to previously
reported wsCV. In conclusion, our protocol allows us to perform DTI on both
upper legs simultaneously with an overall high SNR and high reproducibility.
Introduction
Muscle injuries
comprise a large percentage of sports related injuries and are conventionally
assessed using T2-weighted MR scans. However, current T2-weighted imaging
techniques lack specificity for assessing tissue repair and predicting return
to play1,2. Diffusion Tensor imaging (DTI) can
probe muscle fiber micro-anatomy and has shown to be sensitive to muscle
changes that remained undetected on conventional T2-weighted MRI3. Therefore DTI is suggested as an
advanced diagnostic tool for assessing hamstring injuries. If both upper legs
are scanned simultaneously in muscle injury studies, the muscles in the
uninjured leg can function as a control. However, reaching sufficient
data-quality in both legs using a bilateral protocol is challenging due to B0
and B1+ field inhomogeneities4. As a result, most DTI studies in
the upper legs obtain data from only one leg. In addition, reference values for
the reproducibility of DTI parameter measurements in the hamstrings of healthy
athletes are lacking. Therefore, the aim
of this study was to determine the reproducibility of DTI parameters in the
hamstrings of both legs in healthy athletes over a period of 2 weeks.Methods
This study
was approved by the local IRB and written informed consent was provided. DTI
datasets (See Fig. 1) were acquired in
the upper legs of 10 healthy athletes (9 males-1 female, age range: 22-40, mean
age: 28.2, sports activity: 3x/week). Scans were acquired at 2 time points, 2
weeks apart (day 1 and day 14). A 3T MRI system was used (Ingenia; Philips
Healthcare, Best, the Netherlands). Acquisition parameters are listed in Table 1.
DTI datasets
were processed using DTITools for Wolfram Mathematica (github.com/mfroeling/DTITools).
The DTI data was denoised, registered and corrected for eddy currents and
subject motion. A iterative weighted linear least squares (iWLLS)
approach
was used for the estimation of λ1, λ2 and λ3 from
which Mean diffusivity (MD) and fractional anisotropy (FA) were calculated. The
SNR per muscle was calculated in order to assess DTI quality using a noise map
and the b = 0 s/mm2 data. ROIs
were manually drawn for the Biceps femoris, Semimembranosus and Semitendinosus
muscles in the right and left legs. DTI parameters and SNR are reported per
time point per hamstring muscle as the mean value over the 20 middle slices.
Muscles with SNR<20 at b = 0 s/mm2 were excluded from the
analysis. The statistical analyses comprised one sample T-tests, Bland-Altman
plots and within subject coefficient of variation (wsCV). Results
10 data points were
excluded from analysis because the SNR was below 20. The Bland Altman plots
showed good reproducibility for all DTI parameters (See Figure 2). The within subject Coefficient of Variation (wsCV)
varied between 4.1% and 6.5% for λ1, 3.6% and 6.5% for λ2,
4.1% and 7.2% for λ3, 3.0% and 6.4% for MD and between 8.5% and
13.7% for FA (See Table 2). The wsCV values were similar
for the left and right leg and no left-right bias was detected for λ1,
λ2, λ3, MD, and FA. (one sample T-tests: MD: p=0.549, FA:
p=0.012, λ1: p=0.450, λ2: p=0.404 and λ3: p=0.037).
Figure 3 shows an underestimation of
MD in the lower SNR range. There seems to be no overestimation of FA in the
lower SNR range.Discussion
Our
protocol allows us to perform DTI on both upper legs simultaneously with an
overall high SNR (See Figures 1 and 3) and
high reproducibility for all DTI parameters.
This is demonstrated
by the comparable range in wsCV values between the left and right leg. The range
of reported wsCV values for FA match the values previously reported in the
forearm at 3.0T and the human calf at 1.5T5,6. The wsCV values for λ1,
λ2, λ3 and MD are superior to previously reported wsCV,
which suggests a higher DTI quality compared to previous studies. There are no
DTI reproducibility studies of the upper legs reported in literature for
comparison.Conclusion
Taken
together, these results show that our DTI protocol and post-processing is
robust in both legs and therefore could be applied to assess whether small
changes in DTI parameters due to muscle injury can be detected.Acknowledgements
This project was supported by the ZonMW Sportinnovator grant.References
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