Hollis Crowder1, Valentina Mazzoli2, Marianne Black2, Lauren Watkins3, Feliks Kogan2, Brian Hargreaves4, Marc Levenston4, and Garry Gold4
1Mechanical Engineering, Stanford University, Palo Alto, CA, United States, 2Radiology, Stanford University, Palo Alto, CA, United States, 3Bioengineering, Stanford University, Palo Alto, CA, United States, 4Stanford University, Palo Alto, CA, United States
Synopsis
To identify potential changes in cartilage hydration or microstructure
resulting from exercise we compared global and regional T2 relaxation times of
eleven female recreational runners and five controls at baseline, time 0, and
time 60 minutes post-exercise. No significant difference in mean T2 relaxation
times between the runner group and the control group were found at any time
point in either global or regional analysis. Suspected changes in cartilage
hydration or microstructure resulting from biomechanical running forces may not
manifest in such a way that is detectable by global or regional T2 relaxation
analysis compared to controls.
Synopsis
To identify potential changes in cartilage hydration or microstructure
resulting from exercise we compared global and regional T2 relaxation times of
eleven female recreational runners and five controls at baseline, time 0, and
time 60 minutes post-exercise. No significant difference in mean T2 relaxation
times between the runner group and the control group were found at any time
point in either global or regional analysis. Suspected changes in cartilage
hydration or microstructure resulting from biomechanical running forces may not
manifest in such a way that is detectable by global or regional T2 relaxation
analysis compared to controls.Introduction
Osteoarthritis (OA) is a chronic, debilitating disease
characterized by degenerative changes to joint cartilage1. Running-induced
biomechanical stress in the knee may be a risk factor for developing OA2,
and both reductions and increases in global T2 relaxation times have been
observed in knee cartilage of healthy subjects following various lengths of
time running3,4. The goal of this study is to investigate differences
in global and regional analysis of T2 relaxation times at baseline and during post-activity
scans between recreational runners and control subjects using a novel
quantitative double-echo steady-state (qDESS) sequence. In particular, we
analyzed global and regional T2 relaxation time change of pre-and post-exercise/rest
scans.
Methods
Eleven healthy female recreational runners (20 knees,
22-59yo, 9-25 miles/week, 19.5-24.1 BMI) and five healthy female controls (9
knees, 24-54yo, 0 miles/week, 20.0-24.1 BMI) were included in this study.
Subjects were scanned on a 3T MRI scanner (GE Healthcare, Milwaukie, WI) with a
16-channel flex coil on each knee. Image acquisition used a simultaneous
bilateral qDESS sequence5 with parameters: TR=15.5ms, TE1/TE2=5.2/25.8ms,
1.4mm slice thickness, 256x256 matrix (FOV=160x160mm). Subjects were scanned at
baseline and then at five-minute intervals for 60 minutes following either a 40-minute
run (runner group) or 40-minute rest (control group) (Figure 1). Femoral
cartilage of baseline and Time 0 minutes post-activity (Time 0) scans were
manually segmented using the first echo of qDESS8 (Figure 1) and T2
relaxation values were calculated from the qDESS sequences as previously
described6. T2 maps of continuous scans (Time 5 minutes post-activity
to Time 60 minutes post-activity for a total of 13 T2 maps per knee) were
registered to the Time 0 minutes scans (Elastix rigid registration) 7 (Figure 1). Femoral cartilage T2 projections were created by fitting
segmentations of the 3D T2 maps to a cylinder and then radially projecting the
values into angular bins to generate unrolled maps6 (Figure 2).
Outcomes were reported both as global and regional T2
relaxation times. A mixed effects model with Bonferroni post-hoc comparisons was used to test for
differences in mean T2 relaxation times between the two groups at baseline, and
0 and 60 minutes post-activity in each knee for both superficial and deep
cartilage.Results
A representative progression of unrolled femoral cartilage
T2 relaxation maps for a runner at baseline, time 0 minutes, time 5 minutes, …
time 60 minutes is shown in Figure 3. There were no significant differences (P>0.05)
between the mean T2 relaxation time (ms) of the runner group and the control
group in superficial or deep femoral cartilage layers at Baseline, Time 0
minutes post-activity, or Time 60 minutes post-activity (Figure 4). There were
no significant differences (P>0.05) in
mean T2 relaxation time (ms) between the runner group and the control group at
Baseline, Time 0 minutes, or Time 60 minutes (Figure 5) or between the runner
group and the control group in the anterior, central, or posterior regions of
the femoral cartilage (Figure 5).Discussion
Previously,
significant reductions in T2 relaxation time (ms) have been observed between
Baseline and post-run scans of female recreational runners3.
However, when baseline and post-run scans of female recreational runners
compared with baseline and post-rest scans of healthy controls, there were no
significant differences between the runner group and the control group. Conclusion
Any expected changes in water content resulting from
biomechanical forces of running as indicated by changes in global T2 relaxation
times of femoral cartilage in a population of female healthy recreational
runners may not manifest in such a way that is detectable by global or regional
T2 relaxation analysis compared to controls.Acknowledgements
R01 AR065248-01A1, NIH K24-AR062068-07, NIH R01-AR063643-05,
NIH R00 EB022634
and GE HealthcareReferences
[1] Braun, H J, and Gold, G E. Diagnosis of Osteoarthritis:
Imaging. Bone, August, 2012;51(2):278–288. doi: 10.1016/j.bone. 2011.11.019.
[2] Lane NE, Oehlert JW, Bloch DA, Fries JF. The
relationship of running to osteoarthritis of the knee and hip and bone mineral
density of the lumbar spine: a 9
year longitudinal study. J Rheumatol. 1998; 25 (2):334–41.
PMID: 9489830
[3] Crowder H, Mazzoli V, Black M, et al. Short-Term Effects
of Running on T2 Relaxation Times of Femoral Cartilage in Female Runner. ISMRM,
2019.
[4] Chen M, Qiu L, Shen S, Wang F, Zhang J, Zhang C, et al.
(2017) The influences of walking, running and stair activity on knee articular
cartilage: Quantitative MRI using T1 rho and T2 mapping. PLoS ONE 12(11):
e0187008. https://doi.org/ 10.1371/journal.pone.0187008
[5] Kogan F, Levine E, Chaudhari AC, Monu UD, Epperson K, et
al. Simultaneous Bilateral-Knee MR Imaging. Magnetic resonance in medicine,
2018; 80(2):529-
537. https://doi.org/10.1002/mrm.27045
[6] Black M, Daehyun Y, Young K, et al. Detecting Early
Changes in ACL-Reconstructed Knee Cartilage: Cluster Analysis of T2 Relaxation
Times in Superficial and Deep Cartilage and ADC Analysis. ISMRM, 2019.
[7] S. Klein, M. Staring, K. Murphy, M.A. Viergever,
J.P.W. Pluim, "elastix: a toolbox for intensity based medical image
registration," IEEE Transactions on Medical Imaging, vol. 29, no. 1, pp.
196 - 205, January 2010.
[8] Sveinsson B, Chaudhari AC, Gold GE, Hargreaves BA. A
Simple Analytical Method for Estimating T2 in the Knee From DESS. Magnetic
resonance in
medicine, 2017; 38:63-70. doi: 10.1016/j.mri.2016.12.018.