Recent advances in metabolic imaging

J Nucl Cardiol. 2013 Dec;20(6):1147-72. doi: 10.1007/s12350-013-9786-z.

Abstract

Abnormalities in myocardial substrate metabolism play a central role in the manifestations of most forms of cardiac disease such as ischemic heart disease, heart failure, hypertensive heart disease, and the cardiomyopathy due to either obesity or diabetes mellitus. Their importance is exemplified by both the development of numerous imaging tools designed to detect the specific metabolic perturbations or signatures related to these different diseases, and the vigorous efforts in drug discovery/development targeting various aspects of myocardial metabolism. Since the prior review in 2005, we have gained new insights into how perturbations in myocardial metabolism contribute to various forms of cardiac disease. For example, the application of advanced molecular biologic techniques and the development of elegant genetic models have highlighted the pleiotropic actions of cellular metabolism on energy transfer, signal transduction, cardiac growth, gene expression, and viability. In parallel, there have been significant advances in instrumentation, radiopharmaceutical design, and small animal imaging, which now permit a near completion of the translational pathway linking in-vitro measurements of metabolism with the human condition. In this review, most of the key advances in metabolic imaging will be described, their contribution to cardiovascular research highlighted, and potential new clinical applications proposed.

Publication types

  • Review

MeSH terms

  • Cardiovascular Diseases / diagnosis*
  • Fatty Acids / metabolism
  • Humans
  • Insulin Resistance
  • Magnetic Resonance Imaging
  • Magnetic Resonance Spectroscopy
  • Myocardial Ischemia / diagnostic imaging
  • Myocardium / metabolism*
  • Nitric Oxide Synthase Type II / analysis
  • Oxygen Consumption
  • PPAR alpha / analysis
  • Positron-Emission Tomography
  • Tomography, Emission-Computed, Single-Photon

Substances

  • Fatty Acids
  • PPAR alpha
  • Nitric Oxide Synthase Type II