Myocardial infarct size and mortality depend on the time of day-a large multicenter study

PLoS One. 2015 Mar 11;10(3):e0119157. doi: 10.1371/journal.pone.0119157. eCollection 2015.

Abstract

Background: Different studies have shown circadian variation of ischemic burden among patients with ST-Elevation Myocardial Infarction (STEMI), but with controversial results. The aim of this study was to analyze circadian variation of myocardial infarction size and in-hospital mortality in a large multicenter registry.

Methods: This retrospective, registry-based study was based on data from AMIS Plus, a large multicenter Swiss registry of patients who suffered myocardial infarction between 1999 and 2013. Peak creatine kinase (CK) was used as a proxy measure for myocardial infarction size. Associations between peak CK, in-hospital mortality, and the time of day at symptom onset were modelled using polynomial-harmonic regression methods.

Results: 6,223 STEMI patients were admitted to 82 acute-care hospitals in Switzerland and treated with primary angioplasty within six hours of symptom onset. Only the 24-hour harmonic was significantly associated with peak CK (p = 0.0001). The maximum average peak CK value (2,315 U/L) was for patients with symptom onset at 23:00, whereas the minimum average (2,017 U/L) was for onset at 11:00. The amplitude of variation was 298 U/L. In addition, no correlation was observed between ischemic time and circadian peak CK variation. Of the 6,223 patients, 223 (3.58%) died during index hospitalization. Remarkably, only the 24-hour harmonic was significantly associated with in-hospital mortality. The risk of death from STEMI was highest for patients with symptom onset at 00:00 and lowest for those with onset at 12:00.

Discussion: As a part of this first large study of STEMI patients treated with primary angioplasty in Swiss hospitals, investigations confirmed a circadian pattern to both peak CK and in-hospital mortality which were independent of total ischemic time. Accordingly, this study proposes that symptom onset time be incorporated as a prognosis factor in patients with myocardial infarction.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circadian Rhythm*
  • Creatine Kinase / metabolism*
  • Hospital Mortality
  • Humans
  • Inpatients
  • Myocardial Infarction / enzymology
  • Myocardial Infarction / mortality*
  • Myocardial Infarction / physiopathology*
  • Prognosis
  • Registries
  • Regression Analysis
  • Retrospective Studies
  • Switzerland / epidemiology
  • Time Factors

Substances

  • Creatine Kinase

Grants and funding

This work was supported by grant from the Faculty of Biology and Medicine of Lausanne, Switzerland [grant for young researcher]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.