Key result
SASHA and SAPPHIRE yield higher T1 mapping accuracy but lower precision than MOLLI and ShMOLLI.
Why the study?
Do SASHA and SAPPHIRE T1 mapping sequences provide better accuracy, precision, and reproducibility compared to MOLLI and ShMOLLI in phantom and healthy subjects?
Observational (n=7)
Do SASHA and SAPPHIRE T1 mapping sequences provide better accuracy, precision, and reproducibility compared to MOLLI and ShMOLLI in phantom and healthy subjects?
Absolute Event Rate: 13% vs 44%
p-value: p=< .05
SASHA and SAPPHIRE T1 mapping sequences offer higher accuracy but lower precision compared to MOLLI and ShMOLLI, while all sequences demonstrate similar reproducibility.
These results should not yet change T1 mapping sequence selection; leaves open validation in patients.
PURPOSE: To compare accuracy, precision, and reproducibility of four commonly used myocardial T1 mapping sequences: modified Look-Locker inversion recovery (MOLLI), shortened MOLLI (ShMOLLI), saturation recovery single-shot acquisition (SASHA), and saturation pulse prepared heart rate independent inversion recovery (SAPPHIRE). MATERIALS AND METHODS: This HIPAA-compliant study was approved by the institutional review board. All subjects provided written informed consent. Accuracy, precision, and reproducibility of the four T1 mapping sequences were first compared in phantom experiments. In vivo analysis was performed in seven healthy subjects (mean age ± standard deviation, 38 years ± 19; four men, three women) who were imaged twice on two separate days. In vivo reproducibility of native T1 mapping and extracellular volume (ECV) were measured. Differences between the sequences were assessed by using Kruskal-Wallis and Wilcoxon rank sum tests (phantom data) and mixed-effect models (in vivo data). RESULTS: T1 mapping accuracy in phantoms was lower with ShMOLLI (62 msec) and MOLLI (44 msec) than with SASHA (13 msec; P < .05) and SAPPHIRE (12 msec; P < .05). MOLLI had similar precision to ShMOLLI (4.0 msec vs 5.6 msec; P = .07) but higher precision than SAPPHIRE (6.8 msec; P = .002) and SASHA (8.7 msec; P < .001). All sequences had similar reproducibility in phantoms (P = .1). The four sequences had similar in vivo reproducibility for native T1 mapping (∼25-50 msec; P > .05) and ECV quantification (∼0.01-0.02; P > .05). CONCLUSION: SASHA and SAPPHIRE yield higher accuracy, lower precision, and similar reproducibility compared with MOLLI and ShMOLLI for T1 measurement. Different sequences yield different ECV values; however, all sequences have similar reproducibility for ECV quantification.
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Roujol et al. (2014) conducted an observational in Healthy subjects (n=7). SASHA and SAPPHIRE T1 mapping sequences vs. MOLLI and ShMOLLI T1 mapping sequences was evaluated on T1 mapping accuracy in phantoms (error in msec) (p=< .05). SASHA and SAPPHIRE yielded higher accuracy (error 13 and 12 msec vs 44 and 62 msec; P<0.05) but lower precision than MOLLI and ShMOLLI for T1 measurement, with similar reproducibility.
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