Bilateral kidney sodium-MRI: Enabling accurate quantification of renal sodium concentration through a two-element phased array system

J Magn Reson Imaging. 2013 Sep;38(3):564-72. doi: 10.1002/jmri.24024. Epub 2013 Feb 6.

Abstract

Purpose: To develop a sodium-MRI ((23) Na-MRI) method for bilateral renal sodium concentration (RSC) measurements in rat kidneys at 9.4 Tesla (T).

Materials and methods: To simultaneously achieve high B1 -field homogeneity and high receive sensitivity a dual resonator system composed of a double-tuned linearly polarized (1) H/(23) Na volume resonator and a newly developed two-element (23) Na receive array was used. In conjunction with three-dimensional (3D) ultra-short Time-to-Echo sequence a quantification accuracy of ± 10% was achieved for a nominal spatial resolution of (1 × 1 × 4) mm(3) in 10 min acquisition time. The technique was applied to study the RSC in six kidneys before and after furosemide-induced diuresis.

Results: The loop diuretic agent induced an increase of cortical RSC by 22% from 86 ± 16 mM to 105 ± 18 mM (P = 0.02), whereas the RSC in the inner medulla decreased by 38% from 213 ± 24 mM to 132 ± 25 mM (P = 0.8×10(-4) ). The RSC changes measured in this study agreed well with the qualitative sodium signal intensity variations reported elsewhere.

Conclusion: Furosemide-induced diuresis has been investigated accurately with herein presented quantitative (23) Na-MRI technique. In the future, RSC quantification could allow for defining pathological and nonpathological RSC ranges to assess sodium concentration changes, e.g., induced by drugs.

Keywords: diuresis; dual resonator system; furosemide; kidney; quantification of sodium concentration; renal 23Na-MRI.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / analysis
  • Diuretics / pharmacology
  • Equipment Design
  • Equipment Failure Analysis
  • Female
  • Furosemide / pharmacology*
  • Kidney / anatomy & histology
  • Kidney / drug effects
  • Kidney / metabolism*
  • Kidney Function Tests / instrumentation*
  • Magnetic Resonance Imaging / instrumentation*
  • Molecular Imaging / instrumentation*
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Sodium / pharmacokinetics*
  • Tissue Distribution

Substances

  • Biomarkers
  • Diuretics
  • Furosemide
  • Sodium