Search tips
Search criteria 


Logo of bmjThis ArticleThe BMJ
BMJ. 2007 May 12; 334(7601): 982.
PMCID: PMC1867899
Head to Head

Should women be offered cholesterol lowering drugs to prevent cardiovascular disease? Yes

Scott M Grundy, professor

Women in western countries are more likely to die from heart disease than from cancer. Scott M Grundy argues that the risks make preventive treatment essential, but Malcolm Kendrick believes the evidence of benefit is not strong enough

Primary and secondary trials show that cholesterol lowering drugs reduce the risk of cardiovascular disease events in men.1 2 Secondary prevention trials in women with established cardiovascular disease also show a reduction in risk.3 4 5 Meta-analyses also show that when all women with or without cardiovascular disease are combined, cholesterol lowering treatment produces benefit.6 7

Some investigators nevertheless argue that women without cardiovascular disease should not be given cholesterol lowering drugs because of insufficient evidence from primary prevention trials in women.8 They speculate that women with and without cardiovascular disease respond differently to the drugs; if true, women may not respond to treatment even when they have the same level of risk as men who do benefit.1 2 This speculation discounts prospective studies showing that raised cholesterol concentration is a major risk factor for first heart attack in both men and women.9

The pathological basis for a difference in response to cholesterol lowering therapy between men and women without cardiovascular disease is difficult to visualise. Atherosclerotic lesions in men and women are indistinguishable pathologically.10 Although women typically develop atherosclerosis more slowly than men, a subgroup of women can be identified that carry the same risk as men.1 Most of these women have multiple cardiovascular risk factors; there is no reliable evidence that they do not benefit from cholesterol lowering.

Level of risk

The current model for preventing cardiovascular disease holds that intensity of therapy should be proportional to absolute risk.1 2 Higher risk patients deserve the most intensive treatment because they experience the greatest reduction in absolute risk in the shortest time and most cost effectively. There is general agreement that both men and women with established cardiovascular disease are at high risk and should get intensive cholesterol lowering therapy.11 12 The US National Cholesterol Education Program guidelines define high risk as a 10 year risk of coronary heart disease greater than 20%.1 2 The essential issue here is whether women as well as men should be considered for cholesterol lowering drugs when their 10 year risk is 10-20%—that is, moderately high. These people will not have established coronary heart disease, and treatment constitutes primary prevention.

Let us consider the magnitude of the issue. Data from the Framingham Offspring Study show that only a few women without cardiovascular disease have a 10 year risk of coronary heart disease over 10%, and most of them are over 60 (table(table).13 Many will be smokers or have diabetes or multiple risk factors. Estimating absolute risk before starting drug therapy will ensure that lower risk women will not be treated inappropriately with drugs.

Distribution of 10 year risks for coronary heart disease from the Framingham offspring study according to age*

Most investigators believe that primary and secondary prevention is an artificial distinction that should give way to a strategy based on absolute risk for future cardiovascular events, regardless of whether previous events have occurred. Clinical trials that have included both men and women at moderately high risk have shown overall risk reduction from cholesterol lowering therapy.14 15 16 But post-hoc analyses limited to women failed to show significant risk reduction because of a lack of statistical power. Not enough women were included to provide a definite result. Some investigators take this result to mean lack of efficacy.8 But without adequate power, the results simply are not informative. The relatively small numbers of women who are at moderately high risk and who are available for clinical trials make it unlikely that a definitive answer will be obtained anytime soon (table(table).). Other approaches to decision making are therefore required.

Acting on evidence

Until a large-scale clinical trial is carried out to test the efficacy of cholesterol lowering in women at moderately high risk we have two options: to exclude such women from drug treatment or to consider treatment based on a combination of clinical trial evidence and epidemiological data. Since a substantial proportion of women ultimately develop cardiovascular disease and die from it, withholding treatment in moderately high risk women that has proved protective in men at similar risk and in women at high risk seems to be stretching the restrictions of “evidence based medicine” beyond reason. The argument that women in the moderately high risk category should be treated with dietary therapy alone is no solution. We have even less clinical trial evidence for benefit of diet treatment in this group than for drug treatment. Of course, to maximise cholesterol lowering, combining dietary therapy with drug treatment is prudent.

In summary, cholesterol lowering drugs should be avoided in most lower risk women. But in those who have multiple cardiovascular risk factors and who are projected to be at moderately high risk, use of drugs such as statins should not be ruled out.


Competing interests: SMG has been a consultant to the following companies that market statins: Merck, Pfizer, Bristol Myers Squibb, and Astra Zeneca.


1. National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Final report. Circulation 2002;106:3143-421. [PubMed]
2. Grundy SM, Cleeman JI, Merz CN, Brewer HB Jr, Clark LT, Hunninghake DB, et al. Implications of recent clinical trials for the National Cholesterol Education Program adult treatment panel III guidelines. Circulation 2004;110:227-39. [PubMed]
3. 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;344:1383-9. [PubMed]
4. Sacks FM, Tonkin AM, Shepherd J, Braunwald E, Cobbe S, Hawkins CM, et al. Effect of pravastatin on coronary disease events in subgroups defined by coronary risk factors: the prospective pravastatin pooling project. Circulation 2000;102:1893-900. [PubMed]
5. Heart Protection Study Collaborative Group. MRC/BHF heart protection study of cholesterol lowering with simvastatin in 20 536 high-risk individuals: a randomised placebo-controlled trial. Lancet 2002;360:7-22. [PubMed]
6. LaRosa JC, He J, Vupputuri S. Effect of statins on risk of coronary disease: a meta-analysis of randomized controlled trials. JAMA 199;282:2340-6.
7. Cholesterol Treatment Trialists' Collaborators. Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90 056 participants in 14 randomised trials of statins. Lancet 2005;366:1267-78. [PubMed]
8. Abramson J, Wright JM. Are lipid-lowering guidelines evidence based? Lancet 2007;369:168-9. [PubMed]
9. Lloyd-Jones DM, Wilson PW, Larson MG, Leip E, Beiser A, D'Agostino RB, et al. Lifetime risk of coronary heart disease by cholesterol levels at selected ages. Arch Intern Med 2003;163:1966-72. [PubMed]
10. McGill HC Jr, McMahan CA, Malcom GT, Oalmann MC, Strong JP. Effects of serum lipoproteins and smoking on atherosclerosis in young men and women. Arterioscler Thromb Vasc Biol 1997;17:95-106. [PubMed]
11. Smith SC Jr, Allen J, Blair SN, Bonow RO, Brass LM, Fonarow GC, et al. AHA/ACC guidelines for secondary prevention for patients with coronary and other atherosclerotic vascular disease: 2006 update: endorsed by the National Heart, Lung, and Blood Institute. Circulation 2006;113:2363-72. [PubMed]
12. De Backer G, Ambrosioni E, Borch-Johnsen K, Brotons C, Cifkova R, Dallongeville J, et al. European guidelines on cardiovascular disease prevention in clinical practice. Third joint task force of European and other societies on cardiovascular disease prevention in clinical practice. Eur Heart J 2003;24:1601-10. [PubMed]
13. Pasternak RC, Abrams J, Greenland P, Smaha LA, Wilson PW, Houston-Miller N. Task force #1—identification of coronary heart disease risk: is there a detection gap? J Am Coll Cardiol 2003;41:1863-74. [PubMed]
14. Shepherd J, Cobbe SM, Ford I, Isles CG, Lorimer AR, MacFarlane PW, et al. Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. N Engl J Med 1995;333:1301-7. [PubMed]
15. 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 Air Force/Texas coronary atherosclerosis prevention study. JAMA 1998;279:1615-22. [PubMed]
16. Sever PS, Dahlof B, Poulter NR, Wedel H, Beevers G, Caulfield M, et al. Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian cardiac outcomes trial--lipid lowering arm (ASCOT-LLA): a multicentre randomised controlled trial. Lancet 2003;361:1149-58. [PubMed]

Articles from The BMJ are provided here courtesy of BMJ Publishing Group