4.4 Review

High-density lipoprotein therapeutics and cardiovascular prevention

Journal

JOURNAL OF CLINICAL LIPIDOLOGY
Volume 4, Issue 5, Pages 411-419

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacl.2010.08.004

Keywords

apoAI; CETP; Cholesterol efflux; HDL; LXR; Reverse cholesterol transport

Funding

  1. Merck
  2. Glaxo
  3. Abbott
  4. Pfizer
  5. ISIS
  6. Astra-Zeneca

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The field of cardiovascular prevention has long anticipated the evolution of high-density lipoprotein (HDL) therapy from unproven metabolic tweaking to pillar of risk reduction on par with low-density lipoprotein control. However, the convincing epidemiologic data linking HDL cholesterol (HDL-C) and cardiovascular disease risk in an inverse correlation has not yet translated into clinical trial evidence supporting linearity between HDL-C increases and risk reduction, or identifying obvious goals of therapy. Although HDL-C-increasing lifestyle maneuvers and established HDL drugs such as niacin and fibrates are likely to protect the vasculature, the negative results obtained in trials of a cholesteryl ester transfer protein inhibitor remind us that HDL-C increases are not always beneficial. It is becoming clear that a functional HDL is a more desirable target than simply increasing HDL-C levels. The larger objective of improving HDL functionality (with or without HDL-C level changes) is bound to become the guiding principle for pharmaceutical research in this area. Several new compounds currently being tested bridge the classical aim of increasing HDL-C levels with the novel target of improving HDL function. (C) 2010 National Lipid Association. All rights reserved.

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