Multiparametric Free-Breathing 3D Whole-Heart Cardiac MR for Anatomical Bright- and Black-Blood Imaging With

Ivan Kokhanovskyi1,2,3,4, Carlos Castillo-Passi3,4,5,6, Michael G Crabb3

  • 1Institute of Diagnostic and Interventional Radiology, School of Medicine and Health, Technische Universität München, Munich, Germany.

NMR in Biomedicine
|May 30, 2026
PubMed

Insights

This study introduces a new low-field MRI technique for comprehensive cardiac assessment, offering high-quality bright- and black-blood imaging and tissue quantification in a single scan. This advance improves accessibility and cost-effectiveness for cardiovascular imaging.

Area of Science:

  • Cardiovascular Magnetic Resonance Imaging
  • Low-Field MRI Technology
  • Quantitative Tissue Characterization

Background:

  • Low-field MRI offers increased accessibility, reduced cost, and improved safety compared to high-field systems.
  • Simultaneous high-resolution bright- and black-blood imaging with quantitative T1/T2 mapping is needed for comprehensive cardiac assessment.
  • Current methods often require multiple scans, limiting efficiency and increasing patient burden.

Purpose of the Study:

  • To develop a novel free-breathing, motion-compensated 3D multi-contrast cardiac MR sequence for simultaneous cardiovascular anatomy and myocardial tissue quantification.
  • To achieve this in a single scan at 0.55 Tesla, aiming for a simple, one-click acquisition.
  • To evaluate the sequence's performance in phantom and in vivo studies against established methods.

Main Methods:

  • A novel 3D multi-contrast sequence using a variable flip angle bSSFP spiral-like readout with 2D image-based navigation for motion correction.
  • Acquisition of six interleaved contrasts for simultaneous bright-blood, black-blood imaging, and joint T1/T2 mapping.
  • Reconstruction via non-rigid motion-corrected iterative SENSE followed by patch-based low-rank denoising.

Main Results:

  • The sequence achieved acquisition, reconstruction, and mapping in approximately 31 minutes.
  • Phantom studies showed small biases in T1 (6.3-23.5 ms) and T2 (0.8-7.3 ms) compared to reference methods.
  • In vivo studies demonstrated statistically similar T1 (648±26 ms) and T2 (56.9±3.2 ms) values compared to established 2D techniques (p > 0.6).

Conclusions:

  • The developed 3D sequence provides high image quality and accurate quantitative mapping at low-field strength.
  • It enables simultaneous comprehensive cardiac assessment, including anatomy and tissue characterization, in a single scan.
  • This technique holds promise for resource-limited settings, enhancing cardiovascular MRI accessibility and efficiency.