These results follow on the heels of findings published recently in the Journal of the American Medical Association suggesting that novel biomarkers such as CRP provided minimal additional value beyond conventional risk factors for assessing cardiovascular risk. "For patients with stable coronary disease who were already on statin therapy, novel biomarkers do not appear to add predictive value over traditional lipid markers such as LDL cholesterol," said Dr. John LaRosa, president and professor of medicine at the State University of New York Downstate Medical Center in Brooklyn, NY, and chair of the TNT steering committee. "Today's analysis adds to the body of evidence that 'traditional' risk factors, including elevated blood cholesterol and blood pressure, as well as cigarette smoking, remain the highest priority targets for reducing cardiovascular risk. Drugs such as atorvastatin, used in this study, have demonstrated effectiveness in accomplishing this goal."
To determine whether levels of biomarkers or lipids after an eight-week run-in period on Lipitor 10 mg were predictive of an increased risk for future cardiovascular events, a nested case-control analysis of the TNT trial was performed. Patients included in the TNT trial had coronary heart disease and were treated with Lipitor. For the analysis, data for 507 patients who experienced a primary event (defined as cardiac death, heart attack, stroke or resuscitated cardiac arrest) were compared with data for 1020 patients who did not experience events.
The 18 novel biomarkers were not predictive of risk for future cardiovascular events in patients with stable coronary heart disease already on statin therapy. Higher levels of LDL cholesterol and triglycerides and lower levels of HDL cholesterol, however, were each strongly and significantly predictive of risk for future events.
About the TNT Study
The original TNT study was an investigator-led trial coordinated by an independent steering committee and funded by Pfizer. The study enrolled 10,001 men and women with coronary heart disease aged 35 years to 75 years in 14 countries and followed them for an average of five years. After an eight week run-in on Lipitor 10 mg, patients were randomized to receive either Lipitor 10 mg or Lipitor 80 mg. Primary study results were published in The New England Journal of Medicine in 2005.
The primary endpoint of the original TNT study was the time to occurrence of a first major cardiovascular event, defined as death from heart disease, non-fatal heart attack, resuscitated cardiac arrest, or fatal or non-fatal stroke.
Lipitor 80 mg is not a starting dose. Lipitor is not approved in all countries to reduce the risk of cardiovascular events in patients with existing heart disease.
Throughout the TNT study, Lipitor was generally well tolerated.
For additional product information, visit www.Lipitor.com.
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