Joanna Langner1, Feliks Kogan1, Bryan Haddock2, and Garry Gold1
1Radiology, Stanford University, Stanford, CA, United States, 2Nuclear Medicine, Copenhagen University Hospital, Copenhagen, Denmark
Synopsis
Increased joint loading is
a known risk factor for progression of osteoarthritis (OA) of the knee.
However, the acute effects of exercise and joint loading are still poorly
understood. Quantitative MRI measures, such as T2 relaxation times, provide an
opportunity to objectively study how exercise affects cartilage matrix
organization and hydration. In this work, we evaluate the feasibility of
measuring acute changes in T2 relaxation times immediately after exercise, in
both knees simultaneously.
INTRODUCTION
Osteoarthritis (OA) is a
widely pervasive chronic degenerative disease of the joint that has a large
physical and financial impact on society, yet remains poorly understood1.
While increased loading is a risk factor for progression of OA of the knee
joint, the short-term effects of exercise are still poorly understood2. MRI
provides a non-invasive way to acquire high-resolution images of the joint.
Further, quantitative measures, such as T2 relaxation times, can provide
objective information regarding changes in cartilage matrix organization and
hydration3. However, studies looking at the effects of exercise on cartilage
T2 relaxation times are often limited by low resolution or SNR as well as analysis
of a single knee or a long duration between the exercise protocol and image
acquisition2,4. The goal of this study was to evaluate the feasibility of
measuring acute changes in T2 relaxation times immediately after exercise, in
both knees simultaneously. METHODS
11 healthy volunteers were
recruited and imaged on a 3.0T scanner (GE Healthcare) with university IRB
approval. Simultaneous bilateral knee imaging was performed before and within
10 minutes after exercise with two 16-channel flexible phased-array extremity
coils (NeoCoil, Pewaukee,WI)5 on both knees (Figure 1). The exercise protocol
had subjects use their right leg to step up onto a 25 cm high stool and then
hop down, landing on a straight left leg, 100 times immediately prior to
imaging (Figure 1b). Images were acquired with a bilateral quantitative
double-echo steady-state (qDESS) sequence (TR/TE1/TE2: 24.6/5.8/43.4 ms, FOV:
16.0 cm, matrix size: 320 x 320, slice thickness: 1.5 mm, number of slices:
220). T2 relaxation time mapping was performed by fitting the two qDESS images
to previously described signal models6. Cartilage in the knee was divided
into eight compartments for segmentation (patellar, trochlear, lateral/medial
central femoral, lateral/medial posterior femoral, and lateral/medial tibial
cartilage). The mean T2 relaxation time from each compartment was calculated
before and after exercise. Differences in cartilage T2 relaxation time before
and after exercise were compared across knees as well as against a null
hypothesis of no change using a Wilcoxon-rank-sum test. RESULTS
Figure 2 shows
representative T2 relaxation time maps before and after exercise, acquired in both
knees simultaneously. The mean changes in T2 relaxation times observed in the
right and left knees were small. In both knees the patellar and trochlear
cartilage showed a slight decrease in T2 relaxation times after exercise, while
all other compartments exhibited a small increase in T2 values after exercise
(Figure 3). In
comparing T2 variations following exercise, the medial femoral and tibial cartilage in the left
leg (landing leg) show the most consistent trend of increasing T2 values
following exercise (p=0.06 in all three compartments). However, none of the
compartmental changes were significant against the null hypothesis of no
change. In comparisons between the two leg exercises, the landing leg (left
leg) showed, on average, larger increases in T2 relaxation times after exercise
compared to the stepping leg (right leg), however these differences were not
statistically significant. DISCUSSION
This study shows the
feasibility of T2 mapping in both knees simultaneously within 10 minutes of an
exercise paradigm. T2 relaxation time mapping provides an objective measure of
how exercise affects cartilage hydration and macromolecule organization. While
we observed a small mean increase in T2 values after exercise, the results were
not statistically significant. This is likely driven by both a small sample
size (N=11) as well as the use of healthy volunteers where proper cartilage
function is expected. Future studies in an OA population may provide important
information about how exercise and knee loading affect proper cartilage
mechanics. It should also be noted that simultaneous bilateral knee imaging in
this study allowed us to analyze two different types of mild exercise, stepping
up and jumping down. More strenuous exercise may have larger and varying
effects on cartilage T2 values and exercise protocols can be tailored to
examine various aspects of joint loading. Further, bilateral imaging allows the
possibility of performing exercise in a single knee and using the contralateral
knee as a control. Analyzing the impact of exercise and loading on the knee
joint could give important insight about the breakdown of proper knee function
and early signs of osteoarthritis.CONCLUSION
We demonstrated in healthy
volunteers the feasibility of cartilage T2 relaxation time mapping, in both
knees simultaneously, within 10 minutes of an exercise paradigm. This may allow
us to study how exercise and joint loading affect proper cartilage mechanics. Acknowledgements
Acknowledgements: This work was funded by GE Healthcare and National Institute
of Health (NIH) grants K99EB022634, R01EB002524, R01AR0063643, and
K24AR062068.References
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