- Poster presentation
- Open Access
In vivo free-breathing DTI & IVIM of the whole human heart using a real-time slice-followed SE-EPI navigator-based sequence: a reproducibility study in healthy volunteers
© Moulin et al; licensee BioMed Central Ltd. 2015
- Published: 3 February 2015
- Fractional Anisotropy
- Diffusion Tensor Image
- Mean Diffusivity
- Diffusion Tensor Image Acquisition
- Grappa Factor
In vivo cardiac diffusion using either the Intra-Voxel Incoherent Motion (IVIM) model or the Diffusion Tensor Imaging (DTI) model shows promise to provide new insights into cardiac disease processes. However, due to the combined challenge of respiratory and heart motion [1, 2], currently proposed acquisition methods may not be applicable in patients due to long acquistion time. In this study, we propose to use the motion information provided by a navigator to prospectively update in real time the position of the diffusion weighted slices, offering an efficient free-breathing strategy for rapid and improved cardiac diffusion acquisition using a single-shot spin-Echo EPI sequence.
The proposed technique was performed on 10 volunteers on 1.5T scanner to quantify the reproducibility of the diffusion parameters (FA, MD, f, D and D*). Double oblique short-axis DW images were acquired with a 128 × 80 pixel matrix and rectangular FoV of 350 × 220mm2. Short axis DW-slices (6-mm-thick) were obtained with an in-plane resolution of 2.7 × 2.7mm2 interpolated in-plane to 1.35 x 1.35mm2; the bandwidth was 2442Hz/pixel, and GRAPPA factor 2 was used. Multiple TDs shifted every 10ms were acquired for PCAtMIP reconstruction. DTI acquisitions parameters were: interleaved 10 contiguous slices; TE=45ms; TR= number of slices x heart rate (e.g., 10s for a heart rate equal to 60 bpm); and 12 diffusion directions with a b-value of 350s/mm2 and 10 TDs for a total acquisition time of 22min. The IVIM acquisition parameters were 5 interleaved slices with a gap of 100%; TE=42ms; TR= 5s; 6 diffusion directions with b-values 0, 15, 30, 50, 75, 100, 200, 300, 400s/mm2 and 5 TDs were acquired for total time of 20min. Inter-measurement reproducibility among repeated measures was assessed by the Lin concordance coefficient (LinCC) and the complementary Bland and Altman method with LinCC coefficient ρc, r (a measure of precision) and Cb (a measure of accuracy).
With a 100% breathing cycle scanning efficiency, the slice-following strategy is a powerful head-foot respiratory motion management solution for SE-EPI cardiac diffusion Vascular fraction f and the diffusion coefficients D and D* were determined to be 35.6±11.9x10-3mm2/s for D*, 1.23±0.19x10-3mm2/s for D and 0.115±0.017 for f. From the DTI protocol, the Mean Diffusivity (MD) was 1.57±0.13x10-3mm2/s and the Fractional Anisotropy (FA) 0.35±0.04. MD (ρ c =0.69,r= 0.70,C b =0.99), D (ρ c =0.92, r=0.99, C b =0.93) and f (ρ c =0.69, r=0.75, C b =0.91) was highly reproducible exept for D* (ρ c =-0.214, r=-0.229, C b =0.93) and FA (ρ c =0.075, r=0.12, C b =0.56) but which remained accurate.
The slice-followed SE-EPI cardiac diffusion sequence is a promising solution for clinical implementation, allowing unprecedent acquisition speed that could be tailored to specific needs.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.