doi: 10.1161/01.CIR.0000014245.25136.D2
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(Circulation. 2002;105:1514.)
© 2002 American Heart Association, Inc.
Cardiology Patient Page |
Statins: Powerful Drugs for Lowering Cholesterol
Advice for Patients
From Weill Medical College of Cornell University, New York, NY.
Correspondence to Antonio M. Gotto, Jr, MD, DPhil, c/o Mr Jesse Jou, Weill Medical College of Cornell University, 445 E 69th St, OH205, New York, NY 10021. E-mail amg_editorial{at}med.cornell.edu
Key Words: lipids • prevention • statins • cholesterol
The underlying cause of heart disease is a process called atherosclerosis. Atherosclerosis has been described simply as hardening of the arteries, but in truth, it involves a complex interaction of biological processes in the walls of arteries. In atherosclerosis, plaque may build up in the vessels that carry blood to the heart (coronary arteries). When one of these plaques tears or ruptures, a blood clot forms that may block the vessel completely and lead to a heart attack (also called a myocardial infarction, or MI, in medical terminology).
One of the key risk factors for the development of atherosclerosis is high cholesterol. Cholesterol is a fatty substance that is a normal component of the cells of the body. Cholesterol (measured in milligrams per deciliter of blood [mg/dL]) is carried through the blood by particles known as lipoproteins, which are classified by their densities. The cholesterol in low-density lipoprotein (LDL-C) is called the "bad" cholesterol, and high levels of LDL-C increase the risk for coronary heart disease. Cholesterol in high-density lipoprotein (HDL-C) is called the "good" cholesterol, and high levels of HDL-C decrease the risk for heart attack. High levels of triglycerides, fatty acids that your body uses to store energy that has been made by the body or obtained from food, also may be associated with increased heart attack risk. Table 1 may be used to help classify your lipid levels, using a scheme developed by the US National Cholesterol Education Program Adult Treatment Panel III.1
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If I have an unfavorable cholesterol profile, what can I do to lower my risk for a heart attack?
High-fat diets are associated with increased cholesterol and increased risk for heart disease. One can reduce these risks with regular exercise and a prudent diet low in animal fat and cholesterol. Dietary modifications may lower the bad cholesterol by about 10%, on average. Aerobic exercise will help strengthen the heart muscle, and such exercise, to the equivalent of running 12 to 15 miles per week, will help raise HDL-C in most people. It is also important to control other risk factors that may be present (Table 2). Whether or not you already have had a heart attack, you should follow a heart-healthy lifestyle program. Many helpful tips can be found on the American Heart Association’s website, www.americanheart.org.
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What if diet and exercise aren’t enough?
When diet and exercise alone are insufficient, drug therapy may help. The most effective and widely tested cholesterol drugs are called the statins, which block the formation of cholesterol in the liver and increase the production of the receptors on liver cells that clean the bad cholesterol from the blood (see the Figure). Five of these drugs are available in the United States: lovastatin, pravastatin, simvastatin, fluvastatin, and atorvastatin. Statins can reduce LDL-C by about 20% to 45%, depending on the dosage and drug. Judging from the results of large, well-conducted clinical trials of lovastatin, pravastatin, and simvastatin, these drugs decrease the risk for heart attack in men and women with both average and high levels of cholesterol, with low levels of the good cholesterol, and before and after a heart attack.2–5 In patients who have had a heart attack, the risk for dying and the risk for stroke are also decreased. Drug therapy, however, does not replace a heart-healthy diet, and lifestyle changes should be continued if a drug is started.
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Statin therapy may be helpful in many kinds of patients (Table 3). However, if you do not fall into any of these categories, you may need to perform a calculation to determine if you are a candidate for statin therapy. This risk calculator and other information for patients from the US National Cholesterol Education Program Adult Treatment Panel III are available online at http://www.nhlbi.nih.gov/guidelines/cholesterol/pat_pub.htm. On the basis of this calculation, you and your physician can decide together whether prescribing a statin is right for you.
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Are statins safe?
All drugs may be associated with potentially serious side effects. When a statin is given at a high dose, there is a risk of 1% to 2% per year for developing abnormalities in liver tests; these are almost always reversible when the drug is stopped or reduced. A much rarer side effect, occurring in somewhere between 1 in 1000 and 1 in 2000 patients, is inflammation of the muscles, called myopathy, in which an enzyme from the muscle leaks into the blood. Doctors and patients alike expressed a great deal of concern when the statin called cerivastatin was withdrawn from the US market in August 2001 because an extreme form of this rare side effect, called rhabdomyolysis, seemed to occur more often in patients receiving cerivastatin. Although this side effect may have been seen more frequently with cerivastatin than with other statins, it should be emphasized that the actual number of cases was very low, considering the millions of prescriptions written for statins since their release.
Although you should discuss these and other safety concerns with your physician, the statins have been shown to be extremely effective in a wide range of men and women and to be very safe when current dosages are used properly under a physician’s supervision. The Heart Protection Study has shown that virtually all categories of individuals with high coronary risk benefit from statin therapy.6 Given how important aspirin can be for reducing the risk for heart disease, it is striking that the lead investigator of this study was confident enough to proclaim the statins as "the new aspirin" (Professor Rory Collins, public communication, 2001). It is clear that the statins are potentially life-saving drugs and that, like aspirin, they should be considered seriously by patients at risk for coronary disease.
Footnotes
Dr Gotto has served as a consultant for the following companies that make or have made statins: AstraZeneca, Bayer, Bristol-Myers Squibb, Merck, Novartis, Pfizer, and Reliant.
References
1.
Expert Panel on the Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults: executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). JAMA. 2001; 285: 2486–2497.
2. Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S). Lancet. 1994; 344: 1383–1389.[CrossRef][Medline] [Order article via Infotrieve]
3.
Sacks FM, Pfeffer MA, Moye LA, et al. The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. N Engl J Med. 1996; 335: 1001–1009.
4.
The Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group. Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels. N Engl J Med. 1998; 339: 1349–1357.
5. Downs JR, Clearfield M, Tyroler HA, et al. Air Force/Texas Coronary Atherosclerosis Prevention Study (AFCAPS/TexCAPS): additional perspectives on tolerability of long-term treatment with lovastatin. Am J Cardiol. 2001; 87: 1074–1079.[CrossRef][Medline] [Order article via Infotrieve]
6.
MRC/BHF Heart Protection Study Collaborative Group. MRC/BHF Heart Protection Study of cholesterol-lowering therapy and of antioxidant vitamin supplementation in a wide range of patients at increased risk of coronary heart disease death: early safety and efficacy experience. Eur Heart J. 1999; 20: 725–74.
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