HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Metabolic rates of ATP transfer through creatine kinase (CK Flux) predict clinical heart failure events and death.

Abstract
Morbidity and mortality from heart failure (HF) are high, and current risk stratification approaches for predicting HF progression are imperfect. Adenosine triphosphate (ATP) is required for normal cardiac contraction, and abnormalities in creatine kinase (CK) energy metabolism, the primary myocardial energy reserve reaction, have been observed in experimental and clinical HF. However, the prognostic value of abnormalities in ATP production rates through CK in human HF has not been investigated. Fifty-eight HF patients with nonischemic cardiomyopathy underwent ³¹P magnetic resonance spectroscopy (MRS) to quantify cardiac high-energy phosphates and the rate of ATP synthesis through CK (CK flux) and were prospectively followed for a median of 4.7 years. Multiple-event analysis (MEA) was performed for HF-related events including all-cause and cardiac death, HF hospitalization, cardiac transplantation, and ventricular-assist device placement. Among baseline demographic, clinical, and metabolic parameters, MEA identified four independent predictors of HF events: New York Heart Association (NYHA) class, left ventricular ejection fraction (LVEF), African-American race, and CK flux. Reduced myocardial CK flux was a significant predictor of HF outcomes, even after correction for NYHA class, LVEF, and race. For each increase in CK flux of 1 μmol g⁻¹ s⁻¹, risk of HF-related composite outcomes decreased by 32 to 39%. These findings suggest that reduced CK flux may be a potential HF treatment target. Newer imaging strategies, including noninvasive ³¹P MRS that detect altered ATP kinetics, could thus complement risk stratification in HF and add value in conditions involving other tissues with high energy demands, including skeletal muscle and brain.
AuthorsPaul A Bottomley, Gurusher S Panjrath, Shenghan Lai, Glenn A Hirsch, Katherine Wu, Samer S Najjar, Angela Steinberg, Gary Gerstenblith, Robert G Weiss
JournalScience translational medicine (Sci Transl Med) Vol. 5 Issue 215 Pg. 215re3 (Dec 11 2013) ISSN: 1946-6242 [Electronic] United States
PMID24337482 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Adenosine Triphosphate
  • Creatine Kinase
Topics
  • Adenosine Triphosphate (metabolism)
  • Adult
  • Cardiomyopathies (enzymology, mortality)
  • Case-Control Studies
  • Creatine Kinase (metabolism)
  • Disease Progression
  • Female
  • Heart (physiopathology)
  • Heart Failure (enzymology, mortality)
  • Humans
  • Magnetic Resonance Spectroscopy
  • Male
  • Middle Aged
  • Myocardium (enzymology)
  • Prospective Studies
  • Risk
  • Treatment Outcome
  • Ventricular Dysfunction, Left (physiopathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: