Purpose To optimize signal-to-noise ratio (SNR) in fast spin echo (rapid acquisition with relaxation enhancement [RARE]) sequences and to improve sensitivity in 19F magnetic resonance imaging (MRI) on a 7T preclinical MRI system, based on a previous experimental evaluation of T 1 and T2 actual relaxation times. Materials and Methods Relative SNR changes were theoretically calculated at given relaxation times (T1, T2) and mapped in RARE parameter space (TR, number of echoes, flip back pulse), at fixed acquisition times. T1 and T 2 of KPF6 phantom samples (solution, agar mixtures, ex vivo perfused brain) were measured and experimental SNR values were compared with simulations, at optimal and suboptimal RARE parameter values. Results The optimized setting largely depended on T1, T2 times and the use of flip back pulse improved SNR up to 30% in case of low T 1/T2 ratios. Relaxation times in different conditions showed negligible changes in T1 (below 14%) and more evident changes in T2 (-95% from water solution to ex vivo brain). Experimental data confirmed theoretical forecasts, within an error margin always below 4.1% at SNR losses of ∼20% and below 8.8% at SNR losses of ∼40%. The optimized settings permitted a detection threshold at a concentration of 0.5 mM, corresponding to 6.22 × 1016 fluorine atoms per voxel. Conclusion Optimal settings according to measured relaxation times can significantly improve the sensitivity threshold in 19F MRI studies. They were provided in a wide range of (T1, T2) values and experimentally validated showing good agreement.

Mastropietro, A., DE BERNARDI, E., Breschi, G., Zucca, I., Cametti, M., Soffientini, C., et al. (2014). Optimization of rapid acquisition with relaxation enhancement (RARE) pulse sequence parameters for 19F-MRI studies. JOURNAL OF MAGNETIC RESONANCE IMAGING, 40(1), 162-170 [10.1002/jmri.24347].

Optimization of rapid acquisition with relaxation enhancement (RARE) pulse sequence parameters for 19F-MRI studies

DE BERNARDI, ELISABETTA;
2014

Abstract

Purpose To optimize signal-to-noise ratio (SNR) in fast spin echo (rapid acquisition with relaxation enhancement [RARE]) sequences and to improve sensitivity in 19F magnetic resonance imaging (MRI) on a 7T preclinical MRI system, based on a previous experimental evaluation of T 1 and T2 actual relaxation times. Materials and Methods Relative SNR changes were theoretically calculated at given relaxation times (T1, T2) and mapped in RARE parameter space (TR, number of echoes, flip back pulse), at fixed acquisition times. T1 and T 2 of KPF6 phantom samples (solution, agar mixtures, ex vivo perfused brain) were measured and experimental SNR values were compared with simulations, at optimal and suboptimal RARE parameter values. Results The optimized setting largely depended on T1, T2 times and the use of flip back pulse improved SNR up to 30% in case of low T 1/T2 ratios. Relaxation times in different conditions showed negligible changes in T1 (below 14%) and more evident changes in T2 (-95% from water solution to ex vivo brain). Experimental data confirmed theoretical forecasts, within an error margin always below 4.1% at SNR losses of ∼20% and below 8.8% at SNR losses of ∼40%. The optimized settings permitted a detection threshold at a concentration of 0.5 mM, corresponding to 6.22 × 1016 fluorine atoms per voxel. Conclusion Optimal settings according to measured relaxation times can significantly improve the sensitivity threshold in 19F MRI studies. They were provided in a wide range of (T1, T2) values and experimentally validated showing good agreement.
Articolo in rivista - Articolo scientifico
19F MRI; molecular imaging; fast spin echo; RARE; pulse sequence optimization; sensitivity threshold
English
13-nov-2013
2014
40
1
162
170
none
Mastropietro, A., DE BERNARDI, E., Breschi, G., Zucca, I., Cametti, M., Soffientini, C., et al. (2014). Optimization of rapid acquisition with relaxation enhancement (RARE) pulse sequence parameters for 19F-MRI studies. JOURNAL OF MAGNETIC RESONANCE IMAGING, 40(1), 162-170 [10.1002/jmri.24347].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/48987
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