PURPOSE: To validate a new saturation recovery single-shot acquisition (SASHA) pulse sequence for T1 mapping and to compare SASHA T1 values in heart failure patients and healthy controls. THEORY: The SASHA sequence consists of 10 electrocardiogram-triggered single-shot balanced steady-state free precession images in a breath-hold. The first image is acquired without magnetization preparation and the remaining nine images follow saturation pulses with variable saturation recovery times. METHODS: SASHA was validated through Bloch equation simulations, Monte Carlo simulations, and phantom experiments. Pre- and postcontrast myocardial and blood T1 values were measured in 29 healthy volunteers and 7 patients with heart failure. RESULTS: SASHA T1 values had excellent agreement (bias, 5 ± 5 ms) with spin echo experiments in phantoms with a wide range of physiologic T1 and T2 values and its accuracy was independent of flip angle, absolute T1 , T2 , and heart rate. The average baseline myocardial T1 in heart failure patients was higher than in healthy controls (1200 ± 32 vs. 1170 ± 9 ms, P < 0.05) at 1.5T, as was the calculated blood-tissue partition coefficient, λ, (0.42 ± 0.04 vs. 0.38 ± 0.02, P < 0.05), consistent with diffuse myocardial fibrosis. CONCLUSIONS: The SASHA sequence is a simple and fast approach to in vivo T1 mapping with good accuracy in simulations and phantom experiments.
PURPOSE: To validate a new saturation recovery single-shot acquisition (SASHA) pulse sequence for T1 mapping and to compare SASHA T1 values in heart failurepatients and healthy controls. THEORY: The SASHA sequence consists of 10 electrocardiogram-triggered single-shot balanced steady-state free precession images in a breath-hold. The first image is acquired without magnetization preparation and the remaining nine images follow saturation pulses with variable saturation recovery times. METHODS: SASHA was validated through Bloch equation simulations, Monte Carlo simulations, and phantom experiments. Pre- and postcontrast myocardial and blood T1 values were measured in 29 healthy volunteers and 7 patients with heart failure. RESULTS: SASHA T1 values had excellent agreement (bias, 5 ± 5 ms) with spin echo experiments in phantoms with a wide range of physiologic T1 and T2 values and its accuracy was independent of flip angle, absolute T1 , T2 , and heart rate. The average baseline myocardial T1 in heart failurepatients was higher than in healthy controls (1200 ± 32 vs. 1170 ± 9 ms, P < 0.05) at 1.5T, as was the calculated blood-tissue partition coefficient, λ, (0.42 ± 0.04 vs. 0.38 ± 0.02, P < 0.05), consistent with diffuse myocardial fibrosis. CONCLUSIONS: The SASHA sequence is a simple and fast approach to in vivo T1 mapping with good accuracy in simulations and phantom experiments.
Authors: Gabriel C Camargo; Tamara Rothstein; Flavia P Junqueira; Elsa Fernandes; Andreas Greiser; Ralph Strecker; Viviani Pessoa; Ronaldo S L Lima; Ilan Gottlieb Journal: Int J Hematol Date: 2016-02-12 Impact factor: 2.490
Authors: Sebastian Weingärtner; Nadja M Meßner; Frank G Zöllner; Mehmet Akçakaya; Lothar R Schad Journal: Magn Reson Med Date: 2016-09-16 Impact factor: 4.668