Abstract
BackgroundMany widely used myocardial T1 mapping sequences use breath-hold acquisitions that limit the precision of calculated T1 maps. The SAturation-recovery single-SHot Acquisition (SASHA) sequence has high accuracy with robustness against systematic confounders, but has poorer precision compared to the commonly used MOdified Look-Locker Inversion recovery (MOLLI) sequence. We propose a novel method for generating high-contrast SASHA images to enable a robust image registration approach to free-breathing T1 mapping with high accuracy and precision.MethodsHigh-contrast (HC) images were acquired in addition to primary variable flip angle (VFA) SASHA images by collecting an additional 15 k-space lines and sharing k-space data with the primary image. The number of free-breathing images and their saturation recovery times were optimized through numerical simulations. Accuracy and precision of T1 maps using the proposed SASHA-HC sequence was compared in 10 volunteers at 1.5 T to MOLLI, a breath-hold SASHA-VFA sequence, and free-breathing SASHA-VFA data processed using conventional navigator gating and standard image registration. Free-breathing T1 maps from 15 patients and 10 volunteers were graded by blinded observers for sharpness and artifacts.ResultsDifference images calculated by subtracting HC and primary SASHA images had greater tissue-blood contrast than the primary images alone, with a 3× improvement for 700 ms TS saturation recovery images and a 6× increase in tissue-blood contrast for non-saturated images. Myocardial T1s calculated in volunteers with free-breathing SASHA-HC were similar to standard breath-hold SASHA-VFA (1156.1 ± 28.1 ms vs 1149.4 ± 26.5 ms, p >0.05). The standard deviation of myocardial T1 values using a 108 s free-breathing SASHA-HC (36.2 ± 3.1 ms) was 50 % lower (p <0.01) than breath-hold SASHA-VFA (72.7 ± 8.0 ms) and 34 % lower (p <0.01) than breath-hold MOLLI (54.7 ± 5.9 ms). T1 map quality scores in volunteers were higher with SASHA-HC (4.7 ± 0.3 out of 5) than navigator gating (3.6 ± 0.4, p <0.01) or normal registration (3.7 ± 0.4, p <0.01). SASHA-HC T1 maps had comparable precision to breath-hold MOLLI using a retrospectively down-sampled 30 s free-breathing acquisition and 30 % higher precision with a 60 s acquisition.ConclusionsHigh-contrast SASHA images enable a robust image registration approach to free-breathing T1 mapping. Free-breathing SASHA-HC provides accurate T1 maps with higher precision than MOLLI in acquisitions longer than 30 s.Electronic supplementary materialThe online version of this article (doi:10.1186/s12968-016-0267-9) contains supplementary material, which is available to authorized users.
Highlights
Many widely used myocardial T1 mapping sequences use breath-hold acquisitions that limit the precision of calculated T1 maps
Saturation-recovery based sequence such SAturation-recovery single-SHot Acquisition (SASHA) [21], Saturation Method using Adaptive Recovery Times (SMART1Map) [22], and SAturation Pulse Prepared Heart rate independent Inversion-REcovery sequence (SAPPHIRE) [23] are more robust to these confounders, but their adoption has been limited by poorer precision which results from reduced dynamic range and signalto-noise compared to the inversion-recovery based MOdified Look-Locker Inversion recovery (MOLLI) sequence [20, 24]
We propose to enable free-breathing saturation recovery single-shot acquisition (SASHA) T1 mapping using image registration by acquiring additional secondary images with higher tissue-blood contrast to improve registration performance
Summary
Many widely used myocardial T1 mapping sequences use breath-hold acquisitions that limit the precision of calculated T1 maps. The SAturation-recovery single-SHot Acquisition (SASHA) sequence has high accuracy with robustness against systematic confounders, but has poorer precision compared to the commonly used MOdified Look-Locker Inversion recovery (MOLLI) sequence. While the MOdified Look-Locker Inversion recovery (MOLLI) technique [15, 16] has gained widespread adoption, it is sensitive to factors such as T2 [17], magnetization transfer [18], and off-resonance [19], and changes in any of these confounders result in changes in measured T1 values [20]. Saturation-recovery based sequence such SAturation-recovery single-SHot Acquisition (SASHA) [21], Saturation Method using Adaptive Recovery Times (SMART1Map) [22], and SAturation Pulse Prepared Heart rate independent Inversion-REcovery sequence (SAPPHIRE) [23] are more robust to these confounders, but their adoption has been limited by poorer precision which results from reduced dynamic range and signalto-noise compared to the inversion-recovery based MOLLI sequence [20, 24]. Higher precision techniques with less variability are needed to reliably detect subtle T1 changes in individual patients and to better identify focal T1 abnormalities
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