Rong Lu1, Tian Xia2, Xiao'ao Xue2, Weijun Tang1, Qing Li3, Caixia Fu4, Ying-Hua Chu3, Esther Raithel5, Tobias Kober6,7,8, Tom Hibert6,7,8, and Tingfang Hwang1
1Radiology, Huashan Hospital, Fudan University, Shanghai, China, 2Sports Medicine, Huashan Hospital, Fudan University, Shanghai, China, 3MR Research Collaboration, Siemens Healthineers Ltd., Shanghai, China, 4Application Developments, Siemens Shenzhen Magnetic Resonance Ltd., 518057 Shenzhen, China, Shanghai, China, 5Siemens Healthineers AG, Forchheim, Berlin, Germany, 6LTS5, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland, 7Department of Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland, 8Advanced Clinical Imaging Technology, Siemens Healthineers International AG, Lausanne, Switzerland
Synopsis
Keywords: Cartilage, MSK
Motivation: The study validated a non-invasive quantitative MR imaging for evaluating cartilage prognostic status after anterior cruciate ligament reconstruction (ACLR) as a technique against arthroscopic and histological measures.
Goal(s): To find the non-invasive biomarkers that can guide treatments and limit post-traumatic osteoarthritis (PTOA) in ACLR patients via quantitative cartilage morphometry analysis and biochemical assessments using GRAPPATINI T2 mapping.
Approach: This was a retrospective cohort study with level II evidence.
Results: Most knee cartilage subregions were thicker, larger in volume, and had higher T2 values in ACLR patients than in healthy controls. Partial cartilage parameters were significantly correlated with clinical scores.
Impact: Quantitative
MRI parameters of cartilage could significantly advance non-invasive diagnosis,
prognostication, and personalized management of cartilage degeneration.
Introduction
Anterior cruciate ligament (ACL) injuries
often lead to post-traumatic osteoarthritis (PTOA), causing long-term pain and
disability. Up to 87% of patients develop PTOA after ACL rupture [1-2]. As
cartilage degeneration is a hallmark of PTOA [3-4], early detection of
cartilage changes after ACL reconstruction (ACLR) could enable better
prognostication and treatment to prevent progression to severe osteoarthritis
(OA).
An accelerated T2 mapping MRI technique called GRAPPATINI
has been proposed [5] and applied for knee cartilage [6]. In this study, we applied
GRAPPATINI in ACLR patients to quantitatively assess their cartilage matrix
composition changes. The morphological properties including cartilage thickness
and volume were efficiently analyzed via a semi-automated segmentation software.
By comparing ACLR patients to healthy controls, we determined the ability of
these imaging biomarkers to detect subtle structural and biochemical cartilage
changes at 6 months after ACLR. Clinical outcome scores were also analyzed.Method
Twenty-five patients with ACLR and twenty-five
propensity-matched individuals without ACLR were enrolled. Each participant’s
operated knee joint was scanned via MRI using a 3 T MRI scanner (MAGNETOM
Prisma, Siemens
Healthineers AG, Erlangen,
Germany) with a 15-channel Tx/Rx knee coil. Participants were required to rest
in a sitting position for 30 minutes before knee joint MRI to ensure that the
cartilage was stable during the scan. Table 1a shows the demographic data
of participants in the normal control (NC) and ACLR groups. Table 1b shows
the MRI sequences and parameters. The morphological imaging included coronal,
axial, sagittal fat-sat, proton-density-weighted (PDWI) and axial T1WI
sequences. The research application GRAPPATNI T2 mapping sequence was performed
in sagittal orientation to quantitatively analyze the knee joint cartilage and
the T2 maps were generated inline. The post-processing research application
(MRChondralHealth v2.1.0, Siemens Healthineers AG, Forchheim, Germany) was used
for segmentation of the cartilage [7]. Patients with ACLR underwent clinical
scoring, including the Tegner, Lysholm, 2000 International Knee Documentation
Committee, and MOCART 2.0 scales. The tibiofemoral and patellofemoral cartilage
in the knee joint were divided into 21 subregions according to anatomical
structure to measure their thickness and volume. Each cartilage subregion was
further divided into three layers according to thickness to measure the T2
values. Either the Student’s t-test or the nonparametric Mann-Whitney U test
was used to analyze the differences in cartilage subregional thickness, volume,
and T2 values between groups. Pearson correlation analysis was used to test the
correlations between cartilage parameters and clinical scales.Results
1. Segmentation:
Automated
segmentation with manual correction was much
faster than fully manual segmentation (~8min vs 1 hour per case) (Fig. 1).
2. Structural Changes:
Cartilage was thicker in ACLR group
compared to controls in 14 subregions, mainly in patellofemoral and medial
tibiofemoral areas. Cartilage volume was larger in ACLR group in femur, tibia,
patella, and 19 subregions (Table 2a-b).
3. Biochemical Changes
T2 values were significantly higher in the ACLR group in
40/84 subregions, indicating cartilage matrix changes. Differences were most
significant in superficial and deep layers. Higher T2 values suggest collagen
disruption and increased hydration (Table 3).
4. Correlations:
The thickness of several subregions
correlated positively with clinical scores. The volume of femoral, tibial, and
patellar subregions correlated with clinical scores. Higher T2 values
correlated negatively with clinical scores in some subregions. Some subregions
showed correlations between T2 values and thickness/volume. (Fig. 2).Discussion
GRAPPATINI T2 mapping allowed accelerated
quantification of cartilage collagen organization and hydration through T2 relaxation
times. Meanwhile, the automated segmentation technique enabled expedited
analysis of morphological properties including cartilage thickness and volume.
At 6 months post-surgery, significant increases were
observed in both T2 values and thickness/volume across many cartilage
subregions. Elevated T2 measures indicated alterations in collagen
matrix and hydration, reflecting early degenerative processes. Conversely,
greater thickness and volume may have resulted from initial reparative cell
proliferation and matrix synthesis. Changes were most prominent in the
superficial and deep layers.
Counterintuitively, some subregions
exhibited reduced T2 values, which may be attributed to increased collagen
production temporarily improving cartilage integrity. However, few correlations
occurred between structural and compositional metrics.Conclusion
This
preliminary study introduced an innovative MRI analysis pipeline to efficiently
provide quantitative structural and functional biomarkers of cartilage health
after ACLR. Broader implementation and validation of this methodology in
sizable ACLR cohorts will now help establish its utility for sensitive
diagnosis, monitoring, and guided treatment of PTOA.Acknowledgements
The MRI sequence and software for this study were supported by Siemens Healthcare AG.References
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