Role of lipoprotein-associated phospholipase A2 in atherosclerosis and its potential as a therapeutic target

61Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Despite substantial progress in preventing adverse cardiovascular events with current therapeutic strategies, there remains an extensive residual risk of clinical events, particularly in high-risk patients. Because of the evidence implicating inflammation in the pathogenesis of atherosclerosis, identifying and targeting inflammatory pathways could help further reduce cardiovascular risk. There has been controversy regarding the role of lipoprotein-associated phospholipase A2 (Lp-PLA2) in atherosclerosis, partly because of the lack of simple animal models with a human-like pattern of Lp-PLA2 lipoprotein distribution. However, accumulating evidence from pathology, biology and epidemiology studies favors a pro-atherogenic rather than an atheroprotective role for the enzyme. In particular, Lp-PLA2 might play an important role in plaque vulnerability. As a result, additional studies are warranted to determine whether Lp-PLA2 inhibition improves plaque stability and ultimately clinical outcomes for high-risk patients. © 2006 Elsevier Ltd. All rights reserved.

Cite

CITATION STYLE

APA

Macphee, C. H., Nelson, J., & Zalewski, A. (2006, April). Role of lipoprotein-associated phospholipase A2 in atherosclerosis and its potential as a therapeutic target. Current Opinion in Pharmacology. https://doi.org/10.1016/j.coph.2005.11.008

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