Lipoprotein-Associated Phospholipase A2 Correlates with Reduced Left Ventricle Ejection Fraction in Hemodialysis Patients

Author:

Jun-Feng Chen1,Xiao-Ping Jin2,Juan Zhang2,Man-Li Yang2,Fan Liu3,Peng Fu1,Qi-Shun Wu4,Yang Shu5,Bo-Lin Si4,Yu-Wen Hu6,Liang Chen2

Affiliation:

1. Department of Nephrology, Shidong Hospital, University of Shanghai for Science and Technology , Shanghai , China

2. Department of Cardiology, Nanjing First Hospital, Nanjing Medical University , Nanjing , China

3. Department of Nephrology, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine , Nanjing , China

4. Department of Nephrology, Affiliated Hospital of Jiangsu University, Jiangsu University , Zhenjiang , China

5. Department of Central Lab, Affiliated Hospital of Jiangsu University, Jiangsu University , Zhenjiang , China

6. Department of Laboratory Medicine, Affiliated Hospital of Jiangsu University, Jiangsu University , Zhenjiang , China

Abstract

Abstract 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.

Funder

Medical Science and Technology Development Foundation

Nanjing Department of Health

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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