Cardiac DTI using short-axis PROPELLER: A feasibility study

Magn Reson Med. 2024 Jun;91(6):2546-2558. doi: 10.1002/mrm.30020. Epub 2024 Feb 20.

Abstract

Purpose: We aimed to develop a free-breathing (FB) cardiac DTI (cDTI) method based on short-axis PROPELLER (SAP) and M2 motion compensated spin-echo EPI (SAP-M2-EPI) to mitigate geometric distortion and eliminate aliasing in acquired diffusion-weighted (DW) images, particularly in patients with a higher body mass index (BMI).

Theory and methods: The study involved 10 healthy volunteers whose BMI values fell into specific categories: BMI <25 (4 volunteers), 25< BMI <28 (5 volunteers), and BMI >30 (1 volunteer). We compared DTI parameters, including fractional anisotropy (FA), mean diffusivity (MD), and helix angle transmurality (HAT), between SAP-M2-EPI and M2-ssEPI. To evaluate the performance of SAP-M2-EPI in reducing geometric distortions in the left ventricle (LV) compared to CINE and M2-ssEPI, we utilized the DICE similarity coefficient (DSC) and assessed misregistration area.

Results: In all volunteers, SAP-M2-EPI yielded high-quality LV DWIs without aliasing, demonstrating significantly reduced geometric distortion (with an average DSC of 0.92 and average misregistration area of 90 mm2) and diminished signal loss due to bulk motion when compared to M2-ssEPI. DTI parameter maps exhibited consistent patterns across slices without motion related artifacts.

Conclusion: SAP-M2-EPI facilitates free-breathing cDTI of the entire LV, effectively eliminating aliasing and minimizing geometric distortion compared to M2-ssEPI. Furthermore, it preserves accurate quantification of myocardial microstructure.

Keywords: PROPELLER MRI; cardiac magnetic resonance; diffusion tensor MRI; distortion correction; free‐breathing; myocardium.

MeSH terms

  • Diffusion Magnetic Resonance Imaging* / methods
  • Diffusion Tensor Imaging* / methods
  • Echo-Planar Imaging / methods
  • Feasibility Studies
  • Heart / diagnostic imaging
  • Heart Ventricles / diagnostic imaging
  • Humans