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NOTE: This article was changed after the paper journal went to press. To read the corrected version follow the link marked "extra: Corrected version" that appears in the contents box at the top of the article.
But caution is needed for young people at low risk of cardiovascular disease
The United States Food and Drug Administration has
recently rejected proposals by the manufacturers of lovastatin and
pravastatin to make these drugs available over the counter. Advisers to
the Food and Drug Administration decided that physicians should
probably determine who should get the drugs as well as monitoring them for side effects. The main arguments for allowing over the counter sales were summarised in a recent conference sponsored by the industry:
statins are effective, easy to take, and relatively safe, and many
people who should be taking these drugs are not doing so.1
The underuse of statins is most apparent in the secondary prevention of
heart disease in patients with known atherosclerotic disease, for whom
there is overwhelming evidence that statins are highly
beneficial.
2 3
In one recent survey, for example, only
37% of patients with recent myocardial infarction and blood cholesterol concentrations above 2 g/l had been given drugs to lower
their lipid concentrations and few had reached their target cholesterol
concentrations.4 Most patients with heart disease have
concentrations of low density lipoprotein cholesterol that warrant
treatment, and making statins available over the counter might increase
their use (as has occurred with aspirin).5
Undertreatment is also a problem for the much larger population of
people who do not have manifest atherosclerotic disease (primary
prevention). There is no longer any doubt that treatment benefits those
who are at substantial coronary risk. An updated meta-analysis in
this issue of the BMJ (p 983) shows that drugs that lower
lipid concentrations prevent nearly a third of myocardial infarctions
and coronary deaths.6 All cause mortality was not reduced
significantly, but this is not surprising because statins affect only
cardiovascular mortality,
2 3
and most of the deaths
in people without heart disease were not due to cardiovascular causes.7
Practice guidelines have been devised to identify patients who need
treatment.8 The recently revised Sheffield table is easy
to use and an excellent example. It provides cut-off points for ratios
of total cholesterol to high density lipoprotein cholesterol (based on
age, sex, diabetes, hypertension, and smoking) that identify people
whose coronary risk exceeds 30% per decade.9 The table
also gives cut-off points for treating the larger numbers of people
whose coronary risk exceeds 15% per decade "where resources permit."9 This lower cut-off point has the virtue of
more closely resembling the 10 year coronary risk of participants in
trials of primary prevention.6
Age is the most important determinant of coronary
risk,
10 11
and the two main primary prevention
trials of statins both set the lower limit for enrolment at the
relatively mature ages of 45 for men and 55 for women.6
This decision made sense when designing these trials: younger
participants would have too few coronary events to provide adequate
power to detect an effect of treatment. But in clinical practice
physicians may ask why not extrapolate these results and use statins to
help prevent the few coronary events that do occur in younger people?
Treating younger people may be reasonable if they have other strong
risk factors, such as familial hypercholesterolaemia or diabetes. But the reasons for not doing so in most younger people are the remaining concerns about safety and the harsh realities of cost.
Statins do seem to be reasonably safe and are probably less likely to
cause serious harm than aspirin. Earlier concerns that lipid lowering
drugs might increase the risk of death from injuries were a false
alarm.
2 3
Serious adverse effects such as liver failure and rhabdomyolysis are rare, and more common side effects such
as myositis and raised serum transaminase activity are usually reversible. There remains the theoretical possibility that statins may
have adverse effects years later. A recent follow up report from the
first major trial of statins was reassuring on this point, showing
trends towards continued benefits in survival and fewer cancer deaths
for two years beyond the five years of randomised statin
treatment.12 The evidence for both safety and efficacy have led statins to outstrip other lipid lowering drugs and to eclipse
the role of diet in coronary prevention (which has a far smaller effect
on low density lipoprotein concentration and is resisted by many
patients).13 However, there are two caveats about the
safety of these powerful drugs. Firstly, not every statin has been
studied in large clinical trials with disease end points; use of the
newer formulations is based on surrogate end points and
analogy.14 And secondly, seven years is not long enough to
eliminate concerns about long term adverse effects such as cancer.
While we await the findings of continued follow up of the statin
trials, it is prudent to hold back from prescribing statins for
patients who have a low risk of coronary events over 10 years.
Cost is the other reason to hesitate before recommending statins to
people at low risk of heart disease. Coronary heart disease is so rare
among young adults that starting drug treatment for life in people in
their 30s costs up to £1m ($1.4) per year of life
extended.15 Until the price of statins comes down a lot, this is not a reasonable expenditure of medical resources.
Of course, people who are well off can ignore concerns of cost. In a
world that allows statins to be bought over the counter, they could
also bypass the need to persuade a physician to prescribe them. But the
problems of deciding who should be treated and how to monitor adverse
effects underscore the wisdom of the Food and Drug Administration's
conclusion to leave decisions about taking statins in the hands of
healthcare providers.
However, this does leave us with the obligation to do it right. Many
people who could substantially benefit from statins are not getting
them, perhaps due to a lack of understanding by physicians or to
organisational and fiscal policies that do not support
prevention.
4 16
It is time to get serious about
identifying and removing these obstacles. Physicians must do a better
job of following practice guidelines for using statins to treat
undesirable cholesterol concentrations in people at substantial risk of
coronary events over 10 years, including most patients with a history
of coronary disease and a good many (mostly older) people who may soon
develop it.
Department of Epidemiology, Biostatistics, and Medicine,
University of California San Francisco, School of Medicine, 500 Parnassus Avenue, 420 MU-W, San Francisco, CA 94143-0560, USA
Deborah Grady
Warren S Browner
| 1. | Smith SC. A symposium: expanding the impact of statin therapy: would patients benefit from broader treatment and access? Am J Cardiol 2000; 85: 1-23[Medline]E. |
| 2. | Hebert PR, Gaziano M, Chan KS, Hennekens CH. Cholesterol lowering with statin drugs, risk of stroke, and total mortality: an overview of randomized trials. JAMA 1997; 278: 313-321[Abstract]. |
| 3. | Gordon DJ. Cholesterol lowering reduces mortality: the statins. In: Grundy SM, ed. Cholesterol-lowering therapy: evaluation of clinical trial evidence. New York: Marcel Dekker, 2000:299-311. |
| 4. | Majumdar SR, Gurwitz JH, Soumerai SB. Undertreatment of hyperlipidemia in the secondary prevention of coronary artery disease. J Gen Intern Med 1999; 14: 711-717[CrossRef][Medline]. |
| 5. | Schrott HG, Bittner V, Vittinghoff E, Herrington DM, Hulley S. Adherence to national cholesterol education program treatment goals in postmenopausal women with heart disease. JAMA 1997; 277: 1281-1286[Abstract]. |
| 6. |
Pignone M, Phillips C, Mulrow C.
Use of lipid lowering drugs for primary prevention of coronary heart disese: meta-analysis of randomised trials.
BMJ
2000;
321:
983-986 |
| 7. |
Downs JR, Clearfield M, Weis S, Whitney E, Shapiro DR, Beere PA, et al.
Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels: results of AFCAPS/TexCAPS.
JAMA
1998;
279:
1615-1622 |
| 8. |
Jackson R.
Guidelines on preventing cardiovascular disease in clinical practice.
BMJ
2000;
320:
659-661 |
| 9. |
Wallace EJ, Ramsay LE, Haq I, Ghahramani P, Jackson PR, Rowland-Yeo K, et al.
Coronary and cardiovascular risk estimation for primary prevention: validation of a new Sheffield table in the 1995 Scottish health survey population.
BMJ
2000;
320:
671-676 |
| 10. |
Avins AL, Browner WS.
Improving the prediction of coronary heart disease to aid in the management of high cholesterol levels: what a difference a decade makes.
JAMA
1998;
279:
445-449 |
| 11. |
Ulrich S, Hingorani AD, Martin J, Vallance P.
What is the optimal age for starting lipid lowering treatment? A mathematical model.
BMJ
2000;
320:
1134-1140 |
| 12. | Pedersen TR, Wilhelmsen L, Faergeman O, Strandberg TE, Thorgeirsson G, Troedsson L, et al. Follow-up study of patients randomized in the Scandinavian simvastatin survival study (4S) of cholesterol lowering. Am J Cardiol 2000; 86: 257-262[CrossRef][Medline]. |
| 13. |
Hunninghake DB, Stein EA, Dujovne CA, Harris WS, Feldman EB, Miller VT, et al.
The efficacy of intensive dietary therapy alone or combined with lovastatin in outpatients with hypercholesterolemia.
N Engl J Med
1993;
328:
1213-1219 |
| 14. | Furberg CD, Herrington DM, Psaty BM. Are drugs within a class interchangeable? Lancet 1999; 354: 1202-1204[CrossRef][Medline]. |
| 15. |
Prosser LA, Stinnet AA, Goldman PA, Williams LW, Hunink MGM, Goldman L, et al.
Cost-effectiveness of cholesterol-lowering therapies according to selected patient characteristics.
Ann Intern Med
2000;
132:
769-779 |
| 16. | Hoerger TJ, Bala MV, Bray JW, Wilcosky TC, LaRosa J. Treatment patterns and distribution of low-density lipoprotein cholesterol levels in treatment-eligible United States adults. Am J Cardiol 1998; 82: 61-65[CrossRef][Medline]. |
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