Cell free DNA detected by a novel method in acute ST-elevation myocardial infarction patients

Avi Shimony1, Doron Zahger, Harel Gilutz

  • 1Department of Cardiology, Soroka University Medical Center, Ben Gurion University of the Negev, Beer Sheva, Israel. ashimony@bgu.ac.il;

Acute Cardiac Care
|August 18, 2010
PubMed

Insights

Circulating cell-free DNA (CFD) levels are elevated in ST-elevation myocardial infarction (STEMI) patients. This novel assay shows CFD correlates with cardiac necrosis markers but not ventricular function, warranting further study.

Area of Science:

  • Cardiology
  • Biochemistry
  • Molecular Diagnostics

Background:

  • Elevated circulating cell-free DNA (CFD) indicates poor prognosis in various diseases.
  • Data on CFD in acute myocardial infarction (MI) is limited, with existing detection methods being cumbersome.
  • A novel, rapid fluorometric assay for CFD detection was investigated.

Purpose of the Study:

  • To evaluate a novel method for detecting CFD in ST-elevation myocardial infarction (STEMI) patients.
  • To assess the correlation between CFD levels and established markers of myocardial necrosis.
  • To examine the relationship between CFD and ventricular function.

Main Methods:

  • Serum CFD, troponin-T, and creatine kinase (CK) were measured in 16 STEMI patients and 47 controls.
  • CFD was quantified using a novel rapid fluorometric assay.
  • Ejection fraction (EF) was assessed via echocardiography.

Main Results:

  • Peak CFD levels were significantly higher in STEMI patients versus controls (P=0.001).
  • Peak CFD levels correlated strongly with peak CK (R=0.79) and troponin-T (R=0.65) levels.
  • A trend suggested an association between peak CFD and lower ejection fraction (P=0.075).

Conclusions:

  • The novel CFD assay effectively correlates with myocardial necrosis markers in STEMI.
  • CFD levels did not significantly correlate with ejection fraction in this study.
  • Further research is needed to understand CFD kinetics and prognostic value post-STEMI.
Abstract

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