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Wednesday, 23 July, 2008



Presenter Profile

  Stephen Nicholls, MBBS PhD FRACP FACC The Cleveland Clinic, Ohio, USA

Stephen Nicholls is the Director of the Intravascular Ultrasound Core Laboratory, Clinical Director of the Center for Cardiovascular Diagnostics and Prevention and Associate Director of the Cardiovascular Co-ordinating Center at the Cleveland Clinic. He completed his clinical cardiology fellowship in Australia and undertook his doctoral studies focussing on the anti-inflammatory properties of high-density lipoproteins at the Heart Research Institute at Sydney. This was followed by a postdoctoral fellowship at the Cleveland Clinic Foundation.

Dr Nicholls has co-authored more than 100 original articles, abstracts and book chapters. He is a co-investigator on a number of large clinical trials that employ plaque progression measured by intravascular ultrasound as an endpoint. His research interests include the role of inflammation and lipoproteins in atherogenesis and atherosclerotic plaque imaging.


Recent articles by Stephen Nicholls

Metabolic profiling of arginine and nitric oxide pathways predicts hemodynamic abnormalities and mortality in patients with cardiogenic shock after acute myocardial infarction.
Exposing the complexity of HDL.
Pioglitazone and risk of cardiovascular events in patients with type 2 diabetes mellitus: a meta-analysis of randomized trials.
Protein carbamylation links inflammation, smoking, uremia and atherogenesis.

Presentation

Fighting Atherosclerosis: Recent Advances In Statin Therapy


Conquering Atherosclerosis - From Science to Clinical Practice - Sponsored by AstraZeneca
76th Congress of the European Atherosclerosis Society in Helsinki, Finland
June 11th, 2007


Vascular imaging techniques, such as quantitative coronary angiography, intravascular ultrasound (IVUS), magnetic resonance imaging and B-mode ultrasound, enable us to look inside the vessel wall and detect atherosclerotic disease before the onset of clinical symptoms. Imaging of the vessels also allows the monitoring of change in atherosclerotic burden over time to be evaluated. Consequently, these techniques are useful in assessing the effects of interventions such as lipid-lowering therapies on the atherosclerotic disease process.

Previously, angiography studies established an association between LDL cholesterol (LDL-C) and atherosclerosis progression.1 Recently, a pooled analysis of four IVUS trials demonstrated that increase in HDL cholesterol (HDL-C) level as well as an intensive lowering of LDL-C were independent predictors of atheroma regression.2 In this meta-analysis, substantial regression3 (5% reduction in atheroma volume) was observed in patients with LDL-C levels below the mean (87.5 mg/dL) and percentage increases in HDL-C above the mean (7.5%).

The recent statin imaging trials have made a significant contribution to our understanding of the benefits of statin therapy on the atherosclerotic disease process. They demonstrate that slowing or delaying, and in some instances even regression, of atheroma development can be achieved with effective treatment that combines clinically relevant effects on HDL-C with intensive LDL-C lowering. The effect of therapy on atherosclerosis may be a useful indicator of the impact of interventions on clinical events. The strength of this hypothesis will be discussed.






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