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Plasma B-type natriuretic peptide as a marker of myocardial asynchrony
Katarzyna Ciuraszkiewicz1, Marianna Janion, Dariusz Dudek
1Swietokrzyskie Centrum Kardiologii, Akademia Swietokrzyska, Kielce, Poland.
Insights
Plasma B-type natriuretic peptide (BNP) levels in heart attack patients with intraventricular conduction defects (IVCD) are influenced by left ventricular (LV) asynchrony, especially with preserved LV systolic function.
Area of Science:
- Cardiology
- Biomarkers
- Echocardiography
Background:
- Myocardial infarction (MI) can lead to intraventricular conduction defects (IVCD).
- Myocardial asynchrony is a potential complication in post-MI patients with IVCD.
- B-type natriuretic peptide (BNP) is a biomarker used in heart failure assessment.
Purpose of the Study:
- To evaluate asynchrony parameters in post-MI patients with IVCD.
- To define the relationship between plasma BNP levels and echocardiographic measures of asynchrony.
Main Methods:
- 158 patients 6 months post-MI were studied (126 with IVCD, 32 without).
- Plasma BNP levels were measured using an immunoenzymatic method.
- Left ventricular (LV) function and asynchrony were assessed via echocardiography.
Main Results:
- Patients with post-MI IVCD exhibited significantly higher interventricular asynchrony and BNP levels compared to those without IVCD.
- In patients with preserved LV ejection fraction (EF) > or =50%, interventricular asynchrony and intraventricular delay significantly impacted BNP levels.
- In patients with reduced LV EF <50%, BNP levels correlated with the magnitude of EF.
Conclusions:
- Plasma BNP levels 6 months post-MI are influenced by LV asynchrony in addition to LV function.
- BNP may serve as a marker of LV asynchrony in post-MI patients with IVCD and preserved LV systolic function.
Objectives:
Myocardial asynchrony in postinfarction patients with intraventricular conduction defects (IVCD) may influence plasma levels of B-type natriuretic peptide (BNP). The aim of the study is to evaluate asynchrony parameters in postinfarction patients with IVCD and to define the relationship between plasma levels of BNP and echocardiographic parameters of asynchrony.
Methods:
The study included 158 patients 6 months after myocardial infarction (MI): 126 patients with IVCD and 32 patients without IVCD. Plasma levels of BNP were measured using an immunoenzymatic method. Left ventricular (LV) function was evaluated in echocardiography.
Results:
In patients with post-MI IVCD, the mean plasma level of BNP was 280.2 +/- 340.2 versus 181.7 +/- 270.4 pg/ml (p < 0.001) and they had significantly higher parameters of interventricular asynchrony as compared with subjects without postinfarction IVCD. Multifactorial regression analysis showed that in patients with an ejection fraction (EF) > or =50%, interventricular asynchrony and intraventricular delay significantly influenced the BNP level. In patients with an EF <50%, BNP levels were correlated with the magnitude of the EF.
Conclusion:
Plasma levels of BNP 6 months after MI depend not only on parameters of LV function but also on LV asynchrony and may serve as its marker in patients with IVCD and preserved LV systolic function.
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