Quantitative susceptibility and T1[formula omitted] mapping of knee articular cartilage at 3T

Abstract

T1ρ and Quantitative Susceptibility Mapping (QSM) are evolving as substrates for quantifying the progressive nature of knee osteoarthritis. ObjectiveTo evaluate the effects of spin lock time combinations on depth-dependent T1ρ estimation, in adjunct to QSM, and characterize the degree of shared variance in QSM and T1ρ for the quantitative measurement of articular cartilage. DesignTwenty healthy participants (10 ​M/10F, 22.2 ​± ​3.4 years) underwent bilateral knee MRI using T1ρ MAPPS sequences with varying TSLs ([0–120] ms), along with a 3D spoiled gradient echo for QSM. Five total TSL combinations were used for T1ρ computation, and direct depth-based comparison. Depth-wide variance was assessed in comparison to QSM as a basis to assess for depth-specific variation in T1ρ computations across healthy cartilage. ResultsLonger T1ρ relaxation times were observed for TSL combinations with higher spin lock times. Depth-specific differences were documented for both QSM and T1ρ, with most change found at ∼60% depth of the cartilage, relative to the surface. Direct squared linear correlation revealed that most T1ρ TSL combinations can explain over 30% of the variability in QSM, suggesting inherent shared sensitivity to cartilage microstructure. ConclusionsT1ρ mapping is subjective to the spin lock time combinations used for computation of relaxation times. When paired with QSM, both similarities and differences in signal sensitivity may be complementary to capture depth-wide changes in articular cartilage.