Abstract

Cardiac diffusion tensor imaging (DTI) is an emerging technique for the in vivo characterisation of myocardial microstructure, and there is a growing need for its validation and standardisation. We sought to establish the accuracy, precision, repeatability and reproducibility of state‐of‐the‐art pulse sequences for cardiac DTI among 10 centres internationally. Phantoms comprising 0%–20% polyvinylpyrrolidone (PVP) were scanned with DTI using a product pulsed gradient spin echo (PGSE; N = 10 sites) sequence, and a custom motion‐compensated spin echo (SE; N = 5) or stimulated echo acquisition mode (STEAM; N = 5) sequence suitable for cardiac DTI in vivo. A second identical scan was performed 1–9 days later, and the data were analysed centrally. The average mean diffusivities (MDs) in 0% PVP were (1.124, 1.130, 1.113) x 10−3 mm2/s for PGSE, SE and STEAM, respectively, and accurate to within 1.5% of reference data from the literature. The coefficients of variation in MDs across sites were 2.6%, 3.1% and 2.1% for PGSE, SE and STEAM, respectively, and were similar to previous studies using only PGSE. Reproducibility in MD was excellent, with mean differences in PGSE, SE and STEAM of (0.3 ± 2.3, 0.24 ± 0.95, 0.52 ± 0.58) x 10−5 mm2/s (mean ± 1.96 SD). We show that custom sequences for cardiac DTI provide accurate, precise, repeatable and reproducible measurements. Further work in anisotropic and/or deforming phantoms is warranted.

Highlights

  • Cardiac diffusion tensor imaging (DTI) is an emerging technique for the in vivo characterisation of myocardial microstructure, and there is a growing need for its validation and standardisation

  • One reported more than two-fold higher signal-to-noise ratio (SNR) efficiency in M2SE compared to STEAM19, while the other, performed on a system with standard clinical gradients, observed that stimulated echo acquisition mode (STEAM) was more robust over a range of cardiac phases20

  • We focus on mean diffusivity (MD); corresponding fractional anisotropy (FA) measurements may be found in Supporting Information

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Summary

Introduction

Cardiac diffusion tensor imaging (DTI) is an emerging technique for the in vivo characterisation of myocardial microstructure, and there is a growing need for its validation and standardisation. Diffusion tensor imaging (DTI) is an emerging non-invasive and contrast agent-free method for the characterisation of cardiac microstructure. It provides measurements, such as mean diffusivity (MD) and fractional anisotropy (FA), that are sensitive to the diffusion of water molecules, and local tissue structure. The second method is based on spin echo (SE) with motion-compensated diffusion gradient waveforms. One reported more than two-fold higher signal-to-noise ratio (SNR) efficiency in M2SE compared to STEAM19, while the other, performed on a system with standard clinical gradients, observed that STEAM was more robust over a range of cardiac phases

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