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IR TrueFISP with a golden-ratio-based radial readout: Fast quantification of T1, T2, and proton density

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Ehses,  P
Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Citation

Ehses, P., Seiberlich, N., Ma, D., Breuer, F., Jakob, P., Griswold, M., et al. (2013). IR TrueFISP with a golden-ratio-based radial readout: Fast quantification of T1, T2, and proton density. Magnetic Resonance in Medicine, 69(1), 71-81. doi:10.1002/mrm.24225.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0013-B51A-8
Abstract
A promising approach for the simultaneous quantification of relative proton density (M0), T1, and T2 is the inversion-recovery TrueFISP sequence, consisting of an inversion pulse followed by a series of balanced steady-state free precession acquisitions. Parameters can then be obtained from a mono-exponential fit to the series of images. However, a segmented acquisition is usually necessary, which increases the total acquisition time considerably. The goal of this study is to obtain M0, T1, and T2 maps using a single-shot acquisition, with T1 and T2 measurements in brain that are consistent with the published literature, with a 20-fold speed improvement over the segmented approach, and at a clinically relevant spatial resolution. To this end, a single-shot inversion-recovery TrueFISP sequence was combined with a radial view-sharing technique. The parameters M0, T1, and T2 were then obtained on a pixel-wise basis from a three fit parameter to the signal evolution. The accuracy of this method for quantifying these parameters is demonstrated in vivo. In addition, further corrections to the quantification necessary owing to other experimental factors, namely magnetization transfer and imperfect slice profiles, were developed. Including additional scans necessary for these corrections in the measurement protocol, the required scan time is increased from approximately 6 to 18-28 s per slice.