Vladimir Juras1,2, Laurent Didier3, Vladimir Mlynarik1, Pavol Szomolanyi1, Stefan Zbyn1, Nicole Getzmann3, Joerg Goldhahn3, Stefan Marlovits4, and Siegfried Trattnig1,5
1Department of Biomedical Imaging and Image-Guided Therapy, High Field MR Centre, Medical University of Vienna, Vienna, Austria, 2Department of Imaging Methods, Institute for Measurement Science, Bratislava, Slovakia, 3Novartis Institutes for Biomedical Research, Basel, Switzerland, 4Department of Traumatology, Medical University of Vienna, Vienna, Austria, 5Christian Doppler Laboratory for Clinical Molecular MR Imaging, Vienna, Austria
Synopsis
An assessment
of the reliability of T2 mapping was achieved with a 3D-TESS
sequence in patients with cartilage lesions ICRS Grade I-II. Since low-grade
cartilage lesions are not usually accompanied by collagen matrix remodeling, we
tested the sensitivity of T2 to detect these lesions at 3 and 7T. It
seems that the reproducibility of 3T T2 mapping is higher than that of
7T; however, the sensitivity of T2 mapping for the detection of low-grade
cartilage lesions was greater at the ultra-high field. T2 mapping
could be used in the future as a good alternative to cartilage biopsies in
future clinical trials on new therapies aimed at cartilage regeneration.INTRODUCTION
Cartilage degeneration or defective
repair after an injury is typically associated with changes in the
macromolecular composition and zonal organization of the cartilage. Thus, the
roughening of the articular surface results from cartilage fibrillation, a
process involving denaturation of the collagen fibril structure and
fragmentation of the collagen network. A complex structure such as the articular
cartilage makes any repair of a defect challenging to monitor, and a
non-invasive approach could then be considered as a good alternative approach
to cartilage biopsies. T2 mapping appears to be well adapted for
the evaluation of the collagen network1; however, the application of
this technique to early degeneration has not yet been validated. Here, we show preliminary results
obtained from an observational study with T2
mapping; the aim was to assess the repeatability and sensitivity of T2 at different field strengths to detect low-grade cartilage
lesions.
MATERIALS AND METHODS
Seven patients (mean
age, 50.3/5.4 years; 2 males/5 females) were imaged, who had confirmed
cartilage defect(s) in the knee joint (ICRS Grade I or II) in the femoral
region. Cartilage T2 mapping was acquired for each of these patients
on both a 3T and a 7T whole-body Siemens MR scanner and repeated after eight days
as a follow-up. T2 relaxation times were 0.25x0.25x3.0 mm3
(3T) and 0.37x0.37x3mm3 (7T) using a 3D-Triple Echo Steady State
sequence (3D-TESS)
2 with the following parameters: TR/TE 11.14/5.06
ms; FA 15°; TA 3:48 min. For image analysis, regions
of interest (ROIs) were defined in 2D-TSE (3T) and 3D-DESS (7T) morphological
images in the region suspicious for a cartilage defect and in a region of
normal-appearing cartilage. These ROIs were then transferred to T2
maps (both 3 T and 7 T). All measurements were repeated eight days later as a part
of a test-retest variability assessment. To compare lesions with reference
cartilage, a paired t-test was used. A P-value lower than 0.05 was considered
statistically significant.
RESULTS
The
mean intra-class correlation coefficient was 0.914 for 3T and 0.638 for 7T
(Fig. 1). At 3T, mean T2 was 38.85±8.5ms in lesions, 34.66±4.2ms in non-weight
bearing cartilage, and 31.21±6.8ms in weight-bearing cartilage. At 7T, mean T2 was 28.73±3.2ms in lesion, 23.26±2.1ms in non-weight
bearing cartilage, and 28.1±3.8ms in weight-bearing cartilage. At both
time-points in all subjects, the T2
of the lesions was higher compared to healthy cartilage; however, statistical
significance was recorded only in case of 7T with eight days of follow-up
(p=0.035; Figs. 2 and 3). There was a tendency toward corrupted zonal stratification
in lesions, but this did not reach statistical significance (Fig. 4).
DISCUSSION
Preliminary results of this study showed that collagen
network disorganization can be detected in patients with low-grade lesions, in our
case, at 7T only. However, the T2 values acquired at 3T
seem to be more robust and repeatable. Interestingly, the T2 in
non-weight bearing zones was lower than the T2 in weight bearing zones at 7T. We attributed this to miscalculated pixels,
which appeared mostly on 7T T2 maps (the reason is unknown at the moment). Zonal variation seems to be
promising marker for the detection of low-grade lesions. This study is
continuing, with more subjects (up to 20) and a three-month follow-up, which will
prospectively validate these preliminary results
CONCLUSION
T2 mapping with 3D-TESS enables monitoring of the changes in low-grade
cartilage lesions and prospective follow-up of patients over time. This might
be a valuable marker for monitoring cartilage development after regenerative
therapy, as it may allow differentiation of the early formation of hyaline from
fibrotic cartilage without resorting to serial biopsies.
Acknowledgements
Funding
support provided by Austrian Science Fund (FWF) P 25246 B24References
1.TJ Mosher et al. Cartilage MRI T2 relaxation time mapping: overview and applications, Seminars in Musculoskeletal Radiology 2004; 8(4):355-368
2.Heule R. et al. Triple echo steady-state (TESS) relaxometry, Magnetic Resonance in Medicine 2004; 71(1) 230–237