Grading knee cartilage degeneration and meniscal injury with combined ACS-accelerated T1ρ and T2 mapping.
Authors
Affiliations (9)
Affiliations (9)
- Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
- Hubei Provincial Clinical Research Center for Precision Radiology & Interventional Medicine, Wuhan, 430022, China.
- Hubei Key Laboratory of Molecular Imaging, Wuhan, 430022, China.
- Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. [email protected].
- Hubei Provincial Clinical Research Center for Precision Radiology & Interventional Medicine, Wuhan, 430022, China. [email protected].
- Hubei Key Laboratory of Molecular Imaging, Wuhan, 430022, China. [email protected].
- Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. [email protected].
- Hubei Provincial Clinical Research Center for Precision Radiology & Interventional Medicine, Wuhan, 430022, China. [email protected].
- Hubei Key Laboratory of Molecular Imaging, Wuhan, 430022, China. [email protected].
Abstract
To evaluate the diagnostic performance of artificial intelligence-compressed sensing (ACS)-accelerated T1ρ mapping combined with conventional T2 mapping for quantitative differentiation of articular cartilage degeneration and meniscal injury severity in knee osteoarthritis (KOA). We prospectively enrolled 56 KOA patients and 30 age-matched healthy volunteers between August 2025 and February 2026. All underwent 3T knee MRI using ACS T1ρ and conventional T2 mapping. Relaxation times were quantified in predefined cartilage and meniscal regions. Cartilage degeneration was classified by Kellgren-Lawrence (K-L) grade: 0 (normal), I-II (mild), and III-IV (severe). Meniscal injury was graded using the Stoller system: 0 (normal), I-II (mild), and III (severe). Group and subgroup comparisons used appropriate statistical tests. T1ρ and T2 values were significantly elevated in KOA versus controls across all regions (P < 0.05). Within KOA, relaxation times differed significantly between mild and severe subgroups (P < 0.05). For cartilage degeneration, AUCs were 0.948 (95% CI: 0.889-1.000) for ACS T1ρ, 0.867 (95% CI: 0.760-0.975) for T2, and 0.964 (95% CI: 0.922-1.000) for the combined model. For meniscal injury, AUCs were 0.851 (95% CI: 0.779-0.922) for ACS T1ρ, 0.802 (95% CI: 0.720-0.885) for T2, and 0.855 (95% CI: 0.784-0.926) for the combined approach. Integrating ACS T1ρ and T2 mapping enables precise, quantitative stratification of cartilage and meniscal pathology across KOA severity levels, offering comprehensive biochemical assessment prior to morphological changes and highlighting its potential for early intervention and stage-based management.