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The robustness of T2 value as a trabecular structural index at multiple spatial resolutions of 7 Tesla MRI

Purpose To evaluate the robustness of MR transverse relaxation times of trabecular bone from spin‐echo and gradient‐echo acquisitions at multiple spatial resolutions of 7 T. Methods The effects of MRI resolutions to T2 and T2* of trabecular bone were numerically evaluated by Monte Carlo simulations....

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Bibliographic Details
Published in:Magnetic resonance in medicine 2018-11, Vol.80 (5), p.1949-1961
Main Authors: Lee, D.K., Song, Y.K., Park, B.W., Cho, H.P., Yeom, J.S., Cho, G., Cho, H.
Format: Article
Language:English
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Summary:Purpose To evaluate the robustness of MR transverse relaxation times of trabecular bone from spin‐echo and gradient‐echo acquisitions at multiple spatial resolutions of 7 T. Methods The effects of MRI resolutions to T2 and T2* of trabecular bone were numerically evaluated by Monte Carlo simulations. T2, T2*, and trabecular structural indices from multislice multi‐echo and UTE acquisitions were measured in defatted human distal femoral condyles on a 7 T scanner. Reference structural indices were extracted from high‐resolution microcomputed tomography images. For bovine knee trabecular samples with intact bone marrow, T2 and T2* were measured by degrading spatial resolutions on a 7 T system. Results In the defatted trabecular experiment, both T2 and T2* values showed strong ( |r| > 0.80) correlations with trabecular spacing and number, at a high spatial resolution of 125 µm3. The correlations for MR image‐segmentation‐derived structural indices were significantly degraded ( |r|  0.95 with respect to approximately 0.4 mm3, 11 minutes) and maintained consistent correlations ( |r| > 0.70) with respect to trabecular spacing (turbo spin echo, 22.5 minutes). Conclusion T2 measurements of trabeculae at 7 T are robust with degrading spatial resolution and may be preferable in assessing trabecular spacing index with reduced scan time, when high‐resolution 3D micro‐MRI is difficult to obtain.
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.27202