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Updated: Jan 24, 2026

Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Circulating lectin pathway proteins do not predict short-term cardiac outcomes after myocardial infarction
C B Holt1,2,3, J A Østergaard1,4, S Thiel2
1Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark.
Insights
Plasma levels of lectin pathway proteins and soluble membrane attack complex do not predict short-term cardiac outcomes after myocardial infarction (MI). C-reactive protein (CRP) showed a negative correlation with left ventricular ejection fraction (LVEF).
Area of Science:
- Cardiology
- Immunology
- Biochemistry
Background:
- Coronary artery disease remains a leading global cause of death, with myocardial infarction (MI) and stroke being primary contributors.
- Inflammation, particularly the complement system, plays a role in the pathogenesis of reperfusion injury following MI.
- New therapeutic strategies targeting inflammation are crucial for managing MI patients.
Purpose of the Study:
- To investigate the association between plasma levels of lectin pathway proteins and myocardial endpoints (left ventricular ejection fraction and infarct size) in ST-elevation myocardial infarction (STEMI) patients.
- To determine if lectin pathway proteins or soluble membrane attack complex (sMAC) can predict short-term cardiac outcomes after STEMI.
Main Methods:
- Plasma samples were collected from 73 STEMI patients post-percutaneous coronary intervention.
- Lectin pathway proteins (mannan-binding lectin, H-ficolin, L-ficolin, M-ficolin), sMAC, and C-reactive protein (CRP) were quantified using immunofluorometric assays.
- Left ventricular ejection fraction (LVEF) and infarct size were assessed via cardiac magnetic resonance imaging 6-9 days post-MI.
Main Results:
- C-reactive protein (CRP) showed a significant negative correlation with LVEF (regression coefficient = -0.17, P = 0.01).
- No significant correlations were found between plasma levels of lectin pathway proteins or sMAC and LVEF or infarct size.
- Plasma levels of these complement components did not differ between patients with LVEF <50% and those with LVEF ≥50%.
Conclusions:
- Pattern-recognition molecules of the lectin complement pathway and sMAC do not serve as predictors of short-term cardiac outcomes in patients with ST-elevation myocardial infarction.
- While CRP correlates with cardiac function post-MI, the lectin pathway does not appear to influence short-term myocardial recovery in this cohort.
Abstract:
Despite improvements in treatment, coronary artery disease is still responsible for one-third of all deaths globally, due predominantly to myocardial infarction (MI) and stroke. There is an important potential in developing new strategies for treatment of patients with these conditions. Inflammation, and in particular the actions of the complement system, has emerged as part of the pathogenesis in reperfusion injury in patients with MI. To further qualify this, we examined the association between the plasma levels of lectin pathway proteins and myocardial end-points, left ventricular ejection fraction (LVEF) and infarct size in a cohort of patients with ST-elevation myocardial infarction (STEMI). A blood sample was drawn the day after percutaneous coronary intervention from 73 patients with STEMI. The primary end-points, LVEF and infarct size, were measured with magnetic resonance imaging 6-9 days after the infarct. Complement pattern-recognition molecules of the lectin pathway (mannan-binding lectin, H-ficolin, L-ficolin and M-ficolin) were analysed along with soluble membrane attack complex (sMAC) and C-reactive protein (CRP) in plasma with immunofluorometric assays <50%. CRP correlated negatively with LVEF, regression coefficient = -0·17 (P = 0·01). None of the lectin pathway proteins correlated to LVEF or infarct size, nor did soluble membrane attack complex (sMAC). There were no differences in plasma levels of these complement proteins when comparing patients with ejection fraction <50% to patients with ejection fraction <50%. Pattern-recognition molecules of the lectin pathway and sMAC do not predict short-term cardiac outcomes after MI.
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