31P nuclear magnetic resonance spectroscopy: a noninvasive tool to monitor metabolic abnormalities in left ventricular hypertrophy in human

Am J Cardiol. 1999 Jun 17;83(12A):19H-24H. doi: 10.1016/s0002-9149(99)00252-0.

Abstract

31p nuclear magnetic resonance (NMR) spectroscopy represents a unique instrument to noninvasively monitor myocardial metabolism in humans. The technique has been used to study the metabolism in myocardial hypertrophy in humans with hypertension, aortic stenosis, aortic incompetence, mitral regurgitation, and hypertrophic cardiomyopathy, as well as after maintenance dialysis or long-term physical exercise in elite cyclists. A primary aim is the determination of the phosphocreatine (PCr)/adenosine triphosphate (ATP) ratio, which reflects the energetic state of the myocardium. Recent investigations take advantage of proton decoupling in 31p NMR spectroscopy, which, besides the PCr/ATP ratio, also allows the determination of the inorganic phosphate/ PCr and the phosphomonoester/PCr ratios as additional indicators for alterations in myocardial metabolism. Abnormal myocardial metabolism was found in humans with aortic stenosis, mitral regurgitation, hypertrophic cardiomyopathy, and in patients who undergo maintenance dialysis. A trend toward a lower PCr/ATP ratio was reported in hypertension and aortic incompetence patients. Several studies have revealed a dependence of the metabolic abnormalities on the degree of heart failure, and one study claimed that a correlation with the extent of hypertrophy exists. No metabolic abnormalities were found in elite cyclists.

Publication types

  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Energy Metabolism*
  • Humans
  • Hypertrophy, Left Ventricular / metabolism*
  • Magnetic Resonance Spectroscopy*
  • Myocardium / metabolism*
  • Phosphates / metabolism
  • Phosphoric Monoester Hydrolases / metabolism
  • Phosphorus Isotopes
  • Reproducibility of Results

Substances

  • Phosphates
  • Phosphorus Isotopes
  • Adenosine Triphosphate
  • Phosphoric Monoester Hydrolases