Key result
Elevated levels of macrophage migration inhibitory factor 24 hours after percutaneous coronary intervention were significantly associated with an increased risk of adverse cardiovascular events at 6 months in patients with ST-segment elevation myocardial infarction.
Why the study?
The study aimed to determine the prognostic role of macrophage migration inhibitory factor (MIF) in the development of STEMI complications within 6 months after the event.
Does the level of macrophage migration inhibitory factor (MIF) predict the development of complications within 6 months in patients with STEMI after successful PCI?
Cohort (n=57)
Yes
Does the level of macrophage migration inhibitory factor (MIF) predict the development of complications within 6 months in patients with STEMI after successful PCI?
Odds Ratio: 1 (95% CI 1.0002–1.0021)
p-value: p=0.022
Early increases in macrophage migration inhibitory factor (MIF) levels, especially when combined with blood glucose, can effectively predict the risk of complications within 6 months after STEMI and successful PCI.
MIF may aid post-PCI STEMI risk stratification; hypothesis-generating and should not yet change practice.
The aim of the study was to determine the prediction role of MIF in development of STEMI complications within 6 months after the event.Materials and methods. The study included 45 people with confirmed myocardial infarction with ST segment elevation (STEMI) and successful restoration of blood flow - TIMI-III. The control group - 12 healthy volunteers. All patients underwent baseline investigation. The level of myocardial damage biomarkers MIF and troponin were determined before percutaneous coronary intervention (PCI), then within 24 hours. The pro-inflammatory CRP biomarker was determined before PCI and 5-7 days after the development of the coronary event. The patient follow-up period was 6 months, during which 8 patients reached the endpoint.Results and discussion. Statistically significant increase of MIF levels in STEMI patients was defined relative to the control group. During the observation period 19% of patients reached the endpoint. The MIFІ level significantly correlated with complications in the acute period of myocardial infarction, the class of acute heart failure according to Killip, with troponin levels, with active smoking, MIFII was correlated with stable angina pectoris before the index event, the size of the left atrium and the mass of the left ventricular myocardium. Assessment of blood glucose in with the MIFII was significant in predicting the development of an adverse outcome, in comparison with a separate biomarker definition, the diagnostic efficiency of the model was 88%.Conclusions. An early increase of MIF level was associated with an adverse course of the disease. Our prognostic model significantly improved the prediction of the risk of complications after STEMI
No takes yet. Share an insight, caveat, or question.
Kopytsya et al. (2019) conducted a cohort in ST-segment elevation myocardial infarction (STEMI) (n=57). Macrophage migration inhibitory factor (MIF) levels vs. Lower MIF levels was evaluated on Combined endpoint of all-cause death, recurrent myocardial infarction, acute stroke, repeat revascularization, or decompensated chronic heart failure at 6 months (OR 1.0, 95% CI 1.0002-1.0021, p=0.022). Elevated levels of macrophage migration inhibitory factor 24 hours after percutaneous coronary intervention were significantly associated with an increased risk of adverse cardiovascular events at 6 months in patients with ST-segment elevation myocardial infarction.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: