Serum levels of Adipocyte fatty acid-binding protein are associated with the severity of coronary artery disease in Chinese women

51Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

Background: Adipocyte fatty acid-binding protein (A-FABP) has been described as a novel adipokine, playing an important role in the development of metabolic syndrome, type 2 diabetes and atherosclerosis. In this study, we investigated the relationship between serum levels of A-FABP and the presence and severity of coronary artery disease (CAD) in Chinese subjects. Methodology/Principal Findings: Circulating A-FABP level was determined by ELISA in 341 Chinese subjects (221 men, 120 women) who underwent coronary angiography. A-FABP levels in patients with CAD were significantly higher compared with non-CAD subjects (P = 0.029 in men; P = 0.031 in women). Serum A-FABP increased significantly in multi-vessel diseased patients than in non-CAD subjects (P = 0.011 in men, P = 0.004 in women), and showed an independent correlation with coronary atherosclerosis index (standardized β = 0.173, P = 0.025). In multiple logistic regression analysis, serum A-FABP was an independent risk factor for CAD in women (OR = 5.637, 95%CI: 1.299-24.457, P = 0.021). In addition, amino terminal pro-brain natriuretic peptide (NT-proBNP) was demonstrated to be positively and independently correlated with A-FABP (standardized β = 0.135, P = 0.027). Conclusions/Significance: Serum A-FABP is closely associated with the presence and severity of CAD in Chinese women. © 2011 Bao et al.

Cite

CITATION STYLE

APA

Bao, Y., Lu, Z., Zhou, M., Li, H., Wang, Y., Gao, M., … Jia, W. (2011). Serum levels of Adipocyte fatty acid-binding protein are associated with the severity of coronary artery disease in Chinese women. PLoS ONE, 6(4). https://doi.org/10.1371/journal.pone.0019115

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free