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Cardiac troponin I for the prediction of functional recovery and left ventricular remodelling following primary percutaneous coronary intervention for ST-elevation myocardial infarction
  1. Jonas Hallén1,
  2. Jesper K Jensen2,
  3. Morten W Fagerland3,
  4. Allan S Jaffe4,
  5. Dan Atar1
  1. 1Department of Cardiology, Oslo University Hospital, Aker and Ullevaal and Faculty of Medicine, University of Oslo, Oslo, Norway
  2. 2Department of Cardiology, Odense University Hospital, Odense, Denmark
  3. 3Department of Research Administration, Oslo University Hospital, Ullevaal, Oslo, Norway
  4. 4Cardiovascular Division, Department of Medicine and Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA
  1. Correspondence to Dr Jonas Hallén, Department of Cardiology, Oslo University Hospital, Aker, Trondheimsveien 235, N-0514 Oslo, Norway; jonashallen{at}gmail.com

Abstract

Objective To investigate the ability of cardiac troponin I (cTnI) to predict functional recovery and left ventricular remodelling following primary percutaneous coronary intervention (pPCI) in ST-elevation myocardial infarction (STEMI).

Design Post hoc study extending from randomised controlled trial.

Patients 132 patients with STEMI receiving pPCI.

Main outcome measures Left ventricular ejection fraction (LVEF), end-diastolic and end-systolic volume index (EDVI and ESVI) and changes in these parameters from day 5 to 4 months after the index event.

Methods Cardiac magnetic resonance examination performed at 5 days and 4 months for evaluation of LVEF, EDVI and ESVI. cTnI was sampled at 24 and 48 h.

Results In linear regression models adjusted for early (5 days) assessment of LVEF, ESVI and EDVI, single-point cTnI at either 24 or 48 h were independent and strong predictors of changes in LVEF (p<0.01), EDVI (p<0.01) and ESVI (p<0.01) during the follow-up period. In a logistic regression analysis for prediction of an LVEF below 40% at 4 months, single-point cTnI significantly improved the prognostic strength of the model (area under the curve = 0.94, p<0.01) in comparison with the combination of clinical variables and LVEF at 5 days.

Conclusion Single-point sampling of cTnI after pPCI for STEMI provides important prognostic information on the time-dependent evolution of left ventricular function and volumes.

Trial Reg No The study was part of a randomised controlled trial http://www.clinicaltrials.gov; Unique identifier: NTC00326976.

  • MRI
  • coronary angioplasty (PCI)
  • STEMI
  • stunned myocardium

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Footnotes

  • Funding JH was supported by grants from the South-Eastern Norway Regional Health Authority, Aker University Hospital Research Foundation and Centre for Heart Failure Research, Oslo, Norway.

  • Competing interests ASJ has consulted over time for most of the major diagnostic companies.

  • Patient consent Obtained.

  • Ethics approval This study was conducted with the approval of all local ethics committees.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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