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Bicomponent Mapping of Cortical Bone Using a New Interleaved UTE Imaging Sequence
- Shin, Soo Hyun;
- Athertya, Jiyo S;
- Suprana, Arya;
- Lo, James;
- Wang, Jiaji;
- Moazamian, Dina;
- Chapelin, Fanny;
- Ma, Yajun
Published Web Location
https://doi.org/10.1002/mrm.70245Abstract
PURPOSE: Ultrashort echo time (UTE) MRI enables direct imaging of cortical bone and quantification of its water compartments via bicomponent T2* modeling. However, conventional approaches require multiple separate dual-echo scans due to limitations in gradient power. This approach is prone to inter-scan inconsistencies such as motion and signal drift, which degrade fitting accuracy. This study proposes an interleaved dual-echo acquisition sequence that acquires multiple echo time (TE) images in a single scan to improve bicomponent T2* quantification in cortical bone. METHODS: The proposed UTE sequence utilizes interleaved dual-echo acquisitions with flexible TE spacings. This sequence was tested on five healthy subjects' tibial midshafts and compared to conventional separate dual-echo scans with and without image registration. Bicomponent T2* modeling was performed, and fitting accuracy was evaluated using normalized-root-mean-squared error (NRMSE). Three subjects were scanned three times to evaluate the scan repeatability. RESULTS: The interleaved method significantly reduced NRMSE (3.2% ± 2.3% vs. 6.2% ± 3.1%, p = 0.0231) and yielded lower and more stable T2* (T2s*; 0.50 ± 0.10 ms vs. 0.76 ± 0.13 ms, p < 0.0001) and fraction (Fs; 78.2 ± 5.1 vs. 84.2% ± 7.1%, p = 0.0006) of short T2 components compared to separate scans without registration. Image registration had a minimal improvement on mapping results for separate scans. Parameter maps from the interleaved scans confirmed more homogeneous distributions of T2s* and Fs with lower fitting errors. The much lower coefficients of variance of the interleaved scans demonstrated improved repeatability compared with separate scans. CONCLUSION: The proposed interleaved UTE dual-echo sequence improves the robustness of bicomponent T2* mapping of the cortical bone by reducing inter-scan inconsistencies.
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