High background levels compromise the use of cardiac troponin I RNA detection in peripheral blood as a diagnostic tool in cardiology

Int J Clin Lab Res. 2000;30(1):13-5. doi: 10.1007/s005990070027.

Abstract

The detection of cardiac troponins in peripheral blood as protein markers of myocardial infarction is a new diagnostic tool in the diagnosis of cardiac disease. In order to increase the sensitivity and specificity of this diagnostic approach, a reverse transcription polymerase chain reaction assay has been developed to detect the mRNA encoding cardiac troponin I from myocardial cells hypothetically released from damaged cardiac tissue. The detection is specific for cardiac troponin I mRNA, with no amplification of homologous sequences of other troponin I isoforms, i.e., troponin I from skeletal muscle cells. However, a strong amplification signal for cardiac troponin I mRNA was detected in samples of peripheral blood from healthy human volunteers. In patients with acute myocardial infarction or angina pectoris, the cardiac troponin I mRNA levels were not increased over background levels. In conclusion, a reverse transcription polymerase chain reaction approach based on the amplification of cardiac troponin I mRNA is not feasible in the diagnosis of cardiac diseases.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Angina Pectoris / blood*
  • Angina Pectoris / diagnosis
  • Angina, Unstable / blood
  • Angina, Unstable / diagnosis
  • Base Sequence
  • Biomarkers
  • Feasibility Studies
  • Humans
  • Molecular Sequence Data
  • Myocardial Infarction / blood*
  • Myocardial Infarction / diagnosis
  • Myocardium / metabolism*
  • Polymerase Chain Reaction
  • Predictive Value of Tests
  • Protein Isoforms / genetics*
  • RNA, Messenger / blood*
  • Sequence Alignment
  • Sequence Homology, Nucleic Acid
  • Troponin I / genetics*

Substances

  • Biomarkers
  • Protein Isoforms
  • RNA, Messenger
  • Troponin I