Abstract

Purpose of this work was to assess feasibility of cardiac diffusion tensor imaging (cDTI) at 7 T in a set of healthy, unfixed, porcine hearts using various parallel imaging acceleration factors and to compare SNR and derived cDTI metrics to a reference measured at 3 T. Magnetic resonance imaging was performed on 7T and 3T whole body systems using a spin echo diffusion encoding sequence with echo planar imaging readout. Five reference (b = 0 s/mm2) images and 30 diffusion directions (b = 700 s/mm2) were acquired at both 7 T and 3 T using a GRAPPA acceleration factor R = 1. Scans at 7 T were repeated using R = 2, R = 3, and R = 4. SNR evaluation was based on 30 reference (b = 0 s/mm2) images of 30 slices of the left ventricle and cardiac DTI metrics were compared within AHA segmentation. The number of hearts scanned at 7 T and 3 T was n = 11. No statistically significant differences were found for evaluated helix angle, secondary eigenvector angle, fractional anisotropy and apparent diffusion coefficient at the different field strengths, given sufficiently high SNR and geometrically undistorted images. R≥3 was needed to reduce susceptibility induced geometric distortions to an acceptable amount. On average SNR in myocardium of the left ventricle was increased from 29±3 to 44±6 in the reference image (b = 0 s/mm2) when switching from 3 T to 7 T. Our study demonstrates that high resolution, ex vivo cDTI is feasible at 7 T using commercial hardware.

Highlights

  • Mechanical [1] and electrical [2] properties of the heart are linked to the myocardial microarchitecture, which exhibits alterations in a broad range of cardiovascular pathologies

  • Our results demonstrate that cardiac DTI (cDTI) in unfixed porcine hearts at 7 T is feasible and can lead to improved SNR in DTI acquisitions of myocardial tissue

  • Comparison to a reference data set of the same hearts measured at 3 T shows that essential DTI features such as helix angle (HA), |E2A|, fractional anisotropy (FA), and apparent diffusion coefficient (ADC), do not significantly change with B0 field strength, given sufficiently high SNR and geometrically undistorted images

Read more

Summary

Introduction

Mechanical [1] and electrical [2] properties of the heart are linked to the myocardial microarchitecture, which exhibits alterations in a broad range of cardiovascular pathologies. In the past years cardiac diffusion imaging, especially cardiac DTI (cDTI), has been established as a nondestructive and non-invasive method for analysis of the microstructure of myocardial tissue. Spin echo based cardiac diffusion MRI at 7T and branching myocytes have been described in ex vivo studies and shown to have high consistency to histological correlation, enabling this method to expand our knowledge of the microstructural basis and progression of cardiovascular diseases. While technical and methodical advances in cDTI gave rise to in vivo applications [10,11,12,13], scan time remains a limiting factor for both angular and spatial resolution. Ex vivo studies, where scan times are unrestricted and no motion and flow factors exist, remain an important research and validation tool in cDTI applications [18,19,20,21]

Objectives
Methods
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call