Dantian Zhu1, Yijie Fang1, Wenhao Wu1, Wenjun Yu1, Wei Li1, Yajun Ma2, and Shaolin Li1
1Department of Radiology, Fifth Affiliated Hospital, SUN Yat-Sen University, Zhuhai, China, 2Department of Radiology, University of California, San Diego, CA, United States
Synopsis
Long-distance
running is a common cause of Achilles tendinopathy. A fast, reliable, and non-invasive magnetic resonance imaging (MRI) technique
to track the early changes in
tendon is of critical importance for effective clinical intervention and
evaluation that can prevent the progression of Achilles tendinopathy. This study aims to evaluate UTE-T2* in the detection of changes in the Achilles tendons of amateur marathon runners before and after long-distance
running.
INTRODUCTION
The Achilles tendon demonstrates low or no signal when
imaged using conventional clinical MRI sequences due to its short transverse
relaxation time[1]. Consequently, Achilles tendon diseases can only be
diagnosed with clinical sequences when morphological changes produce an
increased signal (e.g. rupture, thickening). Quantitative assessment of the
affected biochemical components in tendon could therefore be a potentially
useful tool that facilitates more effective and time-sensitive interventions to
combat the progression of Achilles tendinopathy. This study aims to explore the
value of component Analysis UTE-T2∗ technology on detecting structure changes and dynamic quantitatively
monitoring of amateur marathon athletes' Achilles tendon before and after the
marathon.METHODS
29 amateur
marathon runners were prospectively recruited. The component analysis UTE-T2∗ sequence scans were performed at three
different time points for each subject: (1) pre-race, (2) 48 hours post-race,
and (3) a month post-race. Morphological observation of the Achilles tendon was
performed in different TE sequences. Based on the sagittal position, two
radiologists independently delineated the ROIs in the Achilles tendon and
measured the 3 sub-segments of the Achilles tendon (muscle-tendon junction,
middle, and insertion) and the entire Achilles tendon to obtain T2∗m、T2∗S, T2∗L, and Fraction values.Two-way mixed intraclass
correlation coefficient (ICC) was used to assess the measurement reliability between the two raters. The UTE-T2∗m, T2∗S, T2∗L, and Fraction values of Achilles tendon at three time points were
compared by Friedman M test, the values with statistical differences were
compared by the corrected Bonferroni method. Wilcoxon rank-sum test was used to
compare the difference before and after running with different running postures.RESULTS
The two radiologists had good consistency in measuring
the T2∗m, T2∗S, T2∗L and Fraction values of the Achilles tendon, and the ICC values were
0.957, 0.941, 0.828, and 0.937. In the sequence of short TE (TE≤0.6 ms), the diffuse high signal area appears scattered in
the dotted low signal area(figure 1).The T2∗m, T2∗S and T2∗L values of all areas of the Achilles tendon increased to varying
degrees at 48 hours after marathon exercise, and showed a decreasing trend
after a month of exercise(figure 2&3). Where T2∗s was significantly higher in the Achilles tendon as a whole, in the
muscle-tendon junction and middle segment at 48 h post-race compared to
pre-race, all P < 0.05.DISCUSSION
In this study, we investigated the feasibility of
using quantitative UTE- T2* imaging to assess changes in the Achilles tendon of
29 amateur marathon runners before and after long-distance running. The
Achilles tendon showed high signal intensity on the TE ≤ 0.6ms sequence of UTE,
which could show the scattered spot-like low signal intensity in the diseased
Achilles tendon, which is superior to traditional magnetic resonance imaging. In
this study, it was found that there were varying degrees of increase after
marathon, and gradually returned to the pre-race state after exercise
recovery for more than one month. The difference of T2*s was statistically
significant, which was more sensitive to reflect the biochemical changes of
Achilles tendon before and after exercise than the single-component analysis of
UTE and T2 *L of two components. The early stage of Achilles tendinopathy can be characterized
by the upregulation of large proteoglycans, and an increase of inbound water[3].
When the structure of collagen fiber network was destroyed, the surface area of
exposed collagen fibers expanded, the short T2 water bound to collagen
increased relatively, so the short components of UTE-T2 fibers reflected the
changes of Achilles tendon in the early stage. The changes of tendon connection
segment and middle part of Achilles tendon are more obvious than that of
insertion segment of Achilles tendon. The middle part of the Achilles tendon is
of special interest because this region is relatively low in blood supply. As a
result, tendon diffuse swelling, edema, tenderness, or rupture are not only
more likely to occur in this region, but injuries are relatively slower to
repair than other areas in the tendon[4, 5].CONCLUSION
The Bi-component Analysis UTE-T2∗ technology
is superior to single component analysis in monitoring the dynamic changes of
Achilles tendon before and after exercise, and T2∗S is more sensitive to
subtle changes in chemical composition of Achilles tendon.Acknowledgements
No acknowledgement found.References
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