Theoretical basis for sodium and potassium MRI of the human heart at 1.5 T.

Journal Article (Journal Article)

Knowledge of the extent and location of viable tissue is important to clinical diagnosis. In principle, sodium (23Na) and potassium (39K) MRI could noninvasively provide information about tissue viability. In practice, imaging of these nuclei is difficult because, compared with water protons (1H), 23Na and 39K have lower MR sensitivities (9.2 and 0.051%, respectively), and lower in vivo concentrations (ca. 1000-fold). On the other hand, the relatively short T1 relaxation times of 23Na and 39K (ca. 30 and 10 ms, respectively) suggest that optimized imaging pulse sequences may in part alleviate the weak signal of these nuclei. In this study, numerical simulations of high-speed imaging sequences were developed and used to maximize 23Na and 39K image signal-to-noise ratio (SNR) per unit time within the constraints of existing gradient hardware. The simulation demonstrated that decreasing receiver bandwidth at the expense of echo time (TE) results in a substantial increase in 23Na and 39K image SNR/time despite the short T2 and T2* of these nuclei. Referenced to the available 1H signal on existing 1.5 T scanners, the simulation suggested that it should be possible to acquire three-dimensional 23Na images of the human heart with 7 x 7 x 7 mm resolution and 39K images with 26 x 26 x 26 mm resolution in 30 min. Experimentally in humans at 1.5 T, three-dimensional 23Na images of the heart were acquired in 15 min with 6 x 6 x 12 mm resolution and signal-to-noise ratios of 11 and 7 in the left ventricular cavity and myocardium, respectively, which is very similar to the predicted result. The results demonstrate that by choosing imaging pulse sequence parameters that fully exploit the short relaxation times of 23Na and 39K, potassium MRI is improved but remains impractical, whereas sodium MRI improves to the point where 23Na imaging of the human heart may be clinically feasible on existing 1.5 T scanners.

Full Text

Duke Authors

Cited Authors

  • Parrish, TB; Fieno, DS; Fitzgerald, SW; Judd, RM

Published Date

  • October 1997

Published In

Volume / Issue

  • 38 / 4

Start / End Page

  • 653 - 661

PubMed ID

  • 9324333

International Standard Serial Number (ISSN)

  • 0740-3194

Digital Object Identifier (DOI)

  • 10.1002/mrm.1910380420


  • eng

Conference Location

  • United States