Development of T1 mapping in the myocardium in recent years has demonstrated that the technique can add information to inform the diagnosis or management of patients in a number of pathologies. Sequences have been developed to enable T1 mapping of the myocardium within a single breath-hold and the limitations of these sequences have been well characterized. Recent studies have investigated myocardial T1 mapping in iron overload patients using variants of the MOLLI sequence. These studies have concluded that T1 mapping could be more sensitive and reproducible than T2* mapping for the measurement of iron overload in the myocardium. The current study aims to determine the optimal T1 mapping sequence for iron overload. Simulations, phantom studies and in-vivo studies were carried out to investigate MOLLI and SASHA sequences used for T1 mapping of low T1 and T2 tissues (comparable to iron overload in the myocardium).
Background
Methods
Simulations were performed in Matlab (Mathworks, Natick, MA) using Bloch equations. Modulation of longitudinal and transverse magnetisation was simulated using parameters and timings of the MOLLI and Saturation recovery single‐shot acquisition6 (SASHA) sequences. Simulations were performed with T1 and T2 values characteristic of the healthy, moderately iron-loaded and severely iron-loaded myocardium to demonstrate the effect of read-out and short T1/T2 times on measured T1.
A T1 mapping and Extracellular Volume (ECV) Standardisation in CMR (T1MES) phantom7, containing vials with a range of T1 and T2 values comparable to pathologically shortened and lengthened pre and post-contrast blood and myocardium, was scanned on a 1.5T Philips Ingenia with a 32-channel body coil and a simulated heart-rate of 60 bpm. A standard clinical multi-echo TFE T2* mapping sequence, a SASHA) sequence and two MOLLI 5(3)3 sequences (identical except for flip angle: 35° and 50°) were acquired.
MOLLI, SASHA and T2* mapping sequences with the same parameters as for the phantom, were acquired in a mid short-axis left ventricular slice in 7 healthy volunteers and included in routine clinical scans for 10 patients with known or suspected cardiac iron-overload. Each sequence was repeated 3 times in the healthy volunteers to give an estimate of reproducibility.
ROIs were drawn in the centre of the phantom and the septal myocardium for phantom and in-vivo images, respectively. The mean ROI signal intensities were fitted to recovery and decay curves for each sequence using Osirix (Pixmeo, Switzerland) plugins.
Simulations demonstrated that for MOLLI sequences the signal at maximum TI has a non-linear dependence on T2, suggesting that for very low T2 values the T1 error may become significant, unlike the SASHA sequence which shows a less complex dependence on T2.
Phantom measurements with the SASHA sequence demonstrated a high absolute accuracy (mean absolute error, 1%) and no significant bias towards under- or over-estimation. A larger absolute error was observed with the MOLLI sequence (mean, 7%), with a bias towards underestimation at T1 values >400ms (mean error, -5%).
Inter-study reproducibility, assessed in healthy volunteers, was found to be comparable between T1 mapping sequences (CoV = 1-2.1%), as was inter-subject variation (CoV = 2.6-3.8%).
The number of patients with a low T1, assessed as significantly lower (p<0.05) than healthy volunteer measurements was identical for SASHA and MOLLI sequences (4/10 patients).
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