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Author Spotlight: Exploring the Relationship Between Lipotoxicity and HFpEF
Published on: March 29, 2024
Lipoprotein-Associated Phospholipase A2 Correlates with Reduced Left Ventricle Ejection Fraction in Hemodialysis
Chen Jun-Feng1, Jin Xiao-Ping2, Zhang Juan2
1Department of Nephrology, Shidong Hospital, University of Shanghai for Science and Technology, Shanghai, China.
Insights
Lipoprotein-associated phospholipase A2 (Lp-PLA2) levels are linked to reduced left ventricular ejection fraction (LVEF) in hemodialysis patients. Higher Lp-PLA2 may indicate impaired heart function in this population.
Area of Science:
- Cardiology
- Nephrology
- Biomarkers
Background:
- Reduced left ventricular ejection fraction (LVEF) is prevalent in hemodialysis (HD) patients.
- Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a key factor in cardiovascular events.
Purpose of the Study:
- To investigate the association between Lp-PLA2 and LVEF in HD patients.
- To determine if Lp-PLA2 can serve as a marker for reduced LVEF in this cohort.
Main Methods:
- Fifty-seven HD patients with coronary heart disease were analyzed.
- Blood samples were collected pre- and post-dialysis.
- Patients were grouped by preserved versus reduced LVEF for comparison.
Main Results:
- Higher levels of Lp-PLA2 and C-reactive protein (CRP) were found in patients with reduced LVEF (P ≤ .001).
- Both Lp-PLA2 and CRP showed a negative correlation with LVEF.
- Lp-PLA2 was independently associated with LVEF in multivariate analysis.
Conclusions:
- Lp-PLA2 levels correlate with LVEF in HD patients.
- Lp-PLA2 may aid in evaluating and managing chronic heart failure with reduced LVEF in HD patients for risk stratification.
Objective:
Reduced left ventricular ejection fraction (LVEF) is common in hemodialysis (HD) patients. Lipoprotein-associated phospholipase A2 (Lp-PLA2) is considered an important determinant of cardiovascular events. The aim of the study was to evaluate the relationship between Lp-PLA2 and LVEF in HD patients.
Methods:
Fifty-seven HD patients with coronary heart disease were enrolled. Predialysis and postdialysis venous whole blood samples were collected. The patients were divided into preserved and reduced LVEF groups. The relationship between Lp-PLA2 and LVEF was assessed.
Results:
A significant difference in C-reactive protein (CRP) and Lp-PLA2 was observed, with higher levels noted in patients with reduced LVEF (P ≤ .001). Both Lp-PLA2 and CRP were negatively correlated with LVEF in the HD patients. Only Lp-PLA2 remained associated with LVEF in multiple regression analysis.
Conclusion:
Lipoprotein-associated phospholipase A2 levels are associated with LVEF and could potentially be used to evaluate chronic heart failure with reduced LVEF in HD patients for risk stratification management.
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