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Myeloperoxidase in the diagnosis of acute coronary syndromes: The importance of spectrum

  • W. Frank Peacock
  • , John Nagurney
  • , Robert Birkhahn
  • , Adam Singer
  • , Nathan Shapiro
  • , Judd Hollander
  • , Ted Glynn
  • , Richard Nowak
  • , Basmah Safdar
  • , Chadwick Miller
  • , Mary Peberdy
  • , Francis Counselman
  • , Abhinav Chandra
  • , Joshua Kosowsky
  • , James Neuenschwander
  • , Jon Schrock
  • , Stephen Plantholt
  • , Elizabeth Lewandrowski
  • , Vance Wong
  • , Ken Kupfer
  • Deborah Diercks
  • Cleveland Clinic Foundation
  • Massachusetts General Hospital
  • NewYork-Presbyterian Brooklyn Methodist Hospital
  • Beth Israel Deaconess Medical Center
  • University of Pennsylvania
  • Ingham Regional Medical Center
  • Henry Ford Health System
  • Yale University
  • Wake Forest University
  • Virginia Commonwealth University
  • Eastern Virginia Medical School
  • Duke University
  • Brigham and Women’s Hospital
  • Ohio State University
  • Case Western Reserve University
  • St. Agnes Hospital
  • Alere San Diego, Inc.
  • University of California at Davis

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Background: Myeloperoxidase (MPO) is proposed for risk stratification in patients with suspected acute coronary syndromes (ACSs). We determined if MPO has diagnostic value in patients being evaluated for ACS. Method: MIDAS was an 18-center prospective study enrolling suspected ACS emergency department patients who presented <8 hours after symptom onset and in whom serial cardiac markers and objective cardiac perfusion testing were planned. Blinded MPO (Biosite, Inc, San Diego, CA) and troponin I (Triage Cardio 3; Biosite, Inc) were drawn at arrival, and Troponin I (TnI) was measured at 90, 180, and 360 minutes. Final diagnoses were adjudicated by the local investigator blinded to study assay. Results: Of 1,018 patients, 54% were male, 26% black, with a mean age of 58 ± 13 years. Diagnoses were ACS in 288 (23%) and noncardiac chest pain (NCCP) in 788 (77%). Of patients with ACS, 94 (9.2%) had a myocardial infarction (MI) at presentation (69 non-ST-elevation MI, 25 ST-elevation MI), and 136 had unstable angina. Using a cutpoint of 210 ng/mL to provide 90% specificity, MPO had a sensitivity of 0.18; negative predictive value, 0.69; positive predictive value, 0.47; negative likelihood ratio, 0.91; and a positive likelihood ratio of 1.83 to differentiate ACS and NCCP. Because of the large overlap of quartiles, MPO was not clinically useful to predict serial TnI changes. The C statistics ± 95% CI for MPO differentiating ACS from NCCP and for AMI versus NCCP were 0.629 ± 0.04 and 0.666 ± 0.06, respectively. Conclusions: Myeloperoxidase has insufficient accuracy for decision making in patients with suspected ACS.

Original languageEnglish
Pages (from-to)893-899
Number of pages7
JournalAmerican Heart Journal
Volume162
Issue number5
DOIs
StatePublished - Nov 2011

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