Abstract
Purpose of review: The absolute level of HDL cholesterol (HDL-C) may not be the only criterion contributing to their antiatherothrombotic effects. This review focuses on evidence in support of the concept that HDL-bound sphingosine-1-phosphate (S1P) plays a role in different HDL atheroprotective properties and may represent a potential target for therapeutic interventions. Recent findings: Recent large randomized clinical trials testing the hypothesis of raising HDL-C with niacin and dalcetrapib in statin-treated patients failed to improve cardiovascular outcomes. Emerging evidence suggests that many of the cardioprotective functions of HDL, such as vasodilation, angiogenesis and endothelial barrier function, protection against ischemia/reperfusion injury, and inhibition of atherosclerosis, may be attributable to its S1P cargo. HDL-associated S1P may represent a future therapeutic target. Summary: HDL functionality is affected by its composition and there is evidence to suggest S1P plays a role in some of HDL's functions and atheroprotective properties. © 2013 Wolters Kluwer Health.
Original language | English |
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Pages (from-to) | 351-356 |
Number of pages | 5 |
Journal | Current opinion in lipidology |
Volume | 24 |
Issue number | 4 |
DOIs | |
Publication status | Published - Aug 2013 |
Keywords
- Atherothrombotic
- Coronary artery disease
- HDL
- HDL functionality
- Sphingosine-1-phosphate