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Updated: Jul 31, 2025

Quantitative Magnetic Resonance Imaging of Skeletal Muscle Disease
Published on: December 18, 2016
Field inhomogeneity correction for qDESS mapping: application to rapid bilateral knee imaging
Marco Barbieri1, Lauren E Watkins1,2, Valentina Mazzoli1
1Department of Radiology, Stanford University, Stanford, CA, USA.
Purpose:
mapping is a powerful tool for studying osteoarthritis (OA) changes and bilateral imaging may be useful in investigating the role of between-knee asymmetry in OA onset and progression. The quantitative double-echo in steady-state (qDESS) can provide fast simultaneous bilateral knee and high-resolution morphometry for cartilage and meniscus. The qDESS uses an analytical signal model to compute relaxometry maps, which require knowledge of the flip angle (FA). In the presence of inhomogeneities, inconsistencies between the nominal and actual FA can affect the accuracy of measurements. We propose a pixel-wise correction method for qDESS < mapping exploiting an auxiliary map to compute the actual FA used in the model.
Methods:
The technique was validated in a phantom and in vivo with simultaneous bilateral knee imaging. measurements of femoral cartilage (FC) of both knees of six healthy participants were repeated longitudinally to investigate the association between variation and .
Results:
The results showed that applying the correction mitigated variations that were driven by inhomogeneities. Specifically, left-right symmetry increased following the correction (= 0.74 > = 0.69). Without the correction, values showed a linear dependence with . The linear coefficient decreased using the correction (from 24.3 ± 1.6 ms to 4.1 ± 1.8) and the correlation was not statistically significant after the application of the Bonferroni correction (p value > 0.01).
Conclusion:
The study showed that correction could mitigate variations driven by the sensitivity of the qDESS mapping method to , therefore, increasing the sensitivity to detect real biological changes. The proposed method may improve the robustness of bilateral qDESS mapping, allowing for an accurate and more efficient evaluation of OA pathways and pathophysiology through longitudinal and cross-sectional studies.

