European Heart Journal Advance Access originally published online on December 8, 2004
European Heart Journal 2005 26(2):107-109; doi:10.1093/eurheartj/ehi042
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European Heart Journal vol. 26 no. 2 © The European Society of Cardiology 2004; all rights reserved.
An evolving story of lipoprotein-associated phospholipase A2 in atherosclerosis and cardiovascular risk prediction
1Department of Vascular Biology, GlaxoSmithKline, 709 Swedeland Road, King of Prussia, PA 19406, USA
2Department of Worldwide Epidemiology, GlaxoSmithKline, Five Moore Drive, Research Triangle Park, NC 27709, USA
* Corresponding author. Tel.: +1 610 270-7227; fax: +1 610 270-6206 E-mail address: colin.h.macphee@gsk.com
This editorial refers to Association of lipoprotein-associated phospholipase A2 levels with coronary artery disease risk factors, angiographic coronary artery disease, and major adverse events at follow-up
by E.S. Brilakis et al., on page 137
| The first 10% of the full text of this article appears below. |
Over the past 50 years, the age-adjusted mortality rate from cardiovascular disease has decreased substantially. Despite the improved mortality rate, there is evidence that actual cardiovascular event rates remain relatively unchanged (i.e. more people are surviving acute events), and heart disease and stroke continue to be leading causes of death in Western societies.1 Intensive research efforts are currently under way with the goal of further reducing the global burden of cardiovascular disease. An improved understanding of vascular biology and the pathogenesis of atherosclerosisincluding the role of inflammatory processesmay prove helpful in achieving this goal.
Atherosclerosis is a condition involving numerous complex processes within the vessel wall that can be characterized as an inflammatory response to injury.
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- Association of lipoprotein-associated phospholipase A2 levels with coronary artery disease risk factors, angiographic coronary artery disease, and major adverse events at follow-up
- Emmanouil S. Brilakis, Joseph P. McConnell, Ryan J. Lennon, Ahmad A. Elesber, Jeffrey G. Meyer, and Peter B. Berger
EHJ 2005 26: 137-144.[Abstract] [FREE Full Text]
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