Current aspects of statins
Journal of Clinical and Basic Cardiology 1999; 2 (2): 203-208
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Keywords: Atherosklerose, Cholesterinsenkung, HMG-CoA-Reduktasehemmung, Koronare Herzkrankheit, Statin, atherosclerosis, cholesterol lowering, coronary artery disease, HMG-CoA-reductase inhibition, Statin
Clinical trials have demonstrated that inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase (statins) significantly reduce cardiovascular-related morbidity and mortality in patients with and without coronary artery disease. Furthermore, statins are currently the most potent cholesterol-lowering drugs available. Subanalyses of the LIPID study have shown that patients suffering from unstable angina pectoris had at least the same benefit from statin therapy as did patients after myocardial infarction. Studies recently published (AVERT) or not published yet (MIRACL) provide more information on the topic of therapy with statins in the early phase of acute coronary syndromes. J Clin Basic Cardiol 1999; 2: 203-8.
Journal of Clinical and Basic Cardiology 1999; 2 (2): 203-208
PDF Summary Figures
Keywords: Atherosklerose, Cholesterinsenkung, HMG-CoA-Reduktasehemmung, Koronare Herzkrankheit, Statin, atherosclerosis, cholesterol lowering, coronary artery disease, HMG-CoA-reductase inhibition, Statin
Clinical trials have demonstrated that inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase (statins) significantly reduce cardiovascular-related morbidity and mortality in patients with and without coronary artery disease. Furthermore, statins are currently the most potent cholesterol-lowering drugs available. Subanalyses of the LIPID study have shown that patients suffering from unstable angina pectoris had at least the same benefit from statin therapy as did patients after myocardial infarction. Studies recently published (AVERT) or not published yet (MIRACL) provide more information on the topic of therapy with statins in the early phase of acute coronary syndromes. J Clin Basic Cardiol 1999; 2: 203-8.
