Key result
Saturation-recovery T1-mapping at 3T yielded significantly higher native T1-times (SAPPHIRE: 1578 ms, SASHA: 1523 ms) compared with MOLLI (1181 ms, p<0.001), demonstrating higher accuracy but slightly lower precision.
Why the study?
Does saturation-recovery T1-mapping at 3T improve accuracy and precision compared to MOLLI in healthy myocardium?
Cross-Sectional (n=20)
Single-blind
Randomized scan order
No
Does saturation-recovery T1-mapping at 3T improve accuracy and precision compared to MOLLI in healthy myocardium?
Absolute Event Rate: 1578% vs 1181%
p-value: p=<0.001
Saturation-recovery T1-mapping at 3T provides higher accuracy and comparable observer variability to MOLLI, establishing reliable reference values for native T1 and ECV in healthy myocardium.
May support saturation-recovery T1-mapping for accurate healthy reference values at 3T; leaves open clinical impact versus MOLLI.
Myocardial T 1 -mapping recently emerged as a promising quantitative method for non-invasive tissue characterization in numerous cardiomyopathies. Commonly performed with an inversion-recovery (IR) magnetization preparation at 1.5T, the application at 3T has gained due to increased quantification precision. Alternatively, saturation-recovery (SR) T 1 -mapping has recently been introduced at 1.5T for improved accuracy. Thus, the purpose of this study is to investigate the robustness and precision of SR T 1 -mapping at 3T and to establish accurate reference values for native T 1 -times and extracellular volume fraction (ECV) of healthy myocardium. Balanced Steady-State Free-Precession (bSSFP) Saturation-Pulse Prepared Heart-rate independent Inversion-REcovery (SAPPHIRE) and Saturation-recovery Single-SHot Acquisition (SASHA) T 1 -mapping were compared with the Modified Look-Locker inversion recovery (MOLLI) sequence at 3T. Accuracy and precision were studied in phantom. Native and post-contrast T 1 -times and regional ECV were determined in 20 healthy subjects (10 men, 27 ± 5 years). Subjective image quality, susceptibility artifact rating, in-vivo precision and reproducibility were analyzed. SR T 1 -mapping showed <4 % deviation from the spin-echo reference in phantom in the range of T 1 = 100–2300 ms. The average quality and artifact scores of the T 1 -mapping methods were: MOLLI:3.4/3.6, SAPPHIRE:3.1/3.4, SASHA:2.9/3.2; (1: poor - 4: excellent/1: strong - 4: none). SAPPHIRE and SASHA yielded significantly higher T 1 -times (SAPPHIRE: 1578 ± 42 ms, SASHA: 1523 ± 46 ms), in-vivo T 1 -time variation (SAPPHIRE: 60.1 ± 8.7 ms, SASHA: 70.0 ± 9.3 ms) and lower ECV-values (SAPPHIRE: 0.20 ± 0.02, SASHA: 0.21 ± 0.03) compared with MOLLI (T 1 : 1181 ± 47 ms, ECV: 0.26 ± 0.03, Precision: 53.7 ± 8.1 ms). No significant difference was found in the inter-subject variability of T 1 -times or ECV-values (T 1 : p = 0.90, ECV: p = 0.78), the observer agreement (inter: p > 0.19; intra: p > 0.09) or consistency (inter: p > 0.07; intra: p > 0.17) between the three methods. Saturation-recovery T 1 -mapping at 3T yields higher accuracy, comparable inter-subject, inter- and intra-observer variability and less than 30 % precision-loss compared to MOLLI.
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Weingärtner et al. (2016) conducted a cross-sectional in Healthy (n=20). Saturation-recovery T1-mapping (SAPPHIRE and SASHA) vs. MOLLI T1-mapping was evaluated on Native T1-times (p=<0.001). Saturation-recovery T1-mapping at 3T yielded significantly higher native T1-times (SAPPHIRE: 1578 ms, SASHA: 1523 ms) compared with MOLLI (1181 ms, p<0.001), demonstrating higher accuracy but slightly lower precision.
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