Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
Paola Primatesta a Department of Epidemiology and Public Health, Royal
Free and University College Medical School, London WC1E 6BT, b Cardiovascular Studies Unit, Department of Clinical
Pharmacology, Imperial College School of Medicine, London W2 1PG
Correspondence to: P
Primatesta paolap{at}public-health.ucl.ac.uk
| |
Abstract |
|---|
|
|
|---|
Objective:
To evaluate the prevalence of the use of
lipid lowering agents and its relation to blood lipid concentrations in
English adults.
Mortality from coronary heart disease in the United Kingdom
is among the highest in the world,1 which is compatible
with the country's high levels of standard risk
factors.
2 3
Until the mid-1990s, the importance of
dyslipidaemia as a risk factor for coronary heart disease was
controversial,4 as was the use of lipid lowering
treatment.5 However, after publication of the 4S trial in
1994,6 four other trials7-10 confirmed
significant reductions in fatal and non-fatal cardiovascular events
when statins were used in both primary
7 8
and secondary
prevention.
6 9 10
National guidelines on use of statins recommend,
11 12
largely on the basis of cost, that lipid lowering drugs be restricted to people with active vascular disease and, in primary prevention, to
those with the highest absolute risk of coronary heart disease, levels that far exceed those at which trials have shown statins to
be effective.8
In light of the national guidelines and evidence on the benefits of
statins (and, more recently, of gemfibrozil),13 we used data from the nationally representative health survey for England in
19982 to evaluate current lipid concentrations in English adults, the proportion of adults receiving lipid lowering medication, and lipid concentrations of adults receiving treatment.
The health survey for England is an annual nationwide
household survey14 that invites the participation of
members of a stratified random sample (drawn from the Royal Mail's
Postcode Address File) that is sociodemographically representative
of the English population. The annual response rate is about 78% of
households overall but is slightly lower among men and in inner cities.
Data are collected at two home visits: one by an interviewer to
administer the questionnaire and one by a nurse to record the use of
prescribed medicines and to take blood samples (among other investigations).
In the 1998 survey smoking habits and any history of
cardiovascular events and diabetes were recorded in the questionnaire. Informants who reported a history of angina or myocardial infarction diagnosed by a doctor were classified as having coronary heart disease.
Standard methods were used to measure concentrations of total
cholesterol and HDL cholesterol from a single non-fasting blood sample
at a central laboratory.15
The most recent UK guidelines on lipid lowering treatment in primary
prevention
11 12 16
recommend treatment for those whose
10 year risk of coronary heart disease is In the 1998 survey, 13 586 adults ( Mean total cholesterol concentrations rose with age among men and
women until the ages of 64 and 74, respectively (table 1). Total
cholesterol concentrations were higher among men than women from age 25 to 54 but not outside this range. HDL cholesterol concentrations were
lower and the mean ratio of total cholesterol to HDL cholesterol was
higher in men than in women at all ages. Of the 10 569 participants
whose cholesterol concentration was measured (including 237 patients on
lipid lowering treatment), 5.8% (95% confidence interval 5.3% to
6.2%) had a concentration
Table 1.
Table 2.
Design:
Cross sectional survey.
Setting:
England, 1998.
Participants:
Nationally representative sample of
13 586 adults (aged
16 years) living in non-institutional households.
Main outcome measures:
Mean blood concentrations
of total cholesterol and high density lipoprotein (HDL) cholesterol,
and the ratio of total cholesterol to HDL cholesterol, in participants
classified by age and sex; prevalence of raised total cholesterol
concentrations and increased ratio of total to HDL cholesterol;
prevalence of use of lipid lowering agents and the lipid concentrations
of people taking them.
Results:
Mean total cholesterol concentrations
were 5.47 (SE 0.02) mmol/l in men and 5.59 (0.02) mmol/l in women. Mean
HDL cholesterol concentrations were 1.28 (0.01) mmol/l in men and 1.55 (0.01) mmol/l in women. Overall, of 10 569 adults who had a valid
cholesterol measurement taken 7133 (67.5%; 95% confidence interval
66.5% to 68.4%) had a total cholesterol concentration
5 mmol/l,
2804 (26.5%; 25.7% to 27.4%) had a ratio of total cholesterol to HDL cholesterol
5 mmol/l, and 237 (2.2%; 1.9% to 2.5%)
reported taking lipid lowering drugs. Of 117 participants with no
history of cardiovascular disease but whose estimated 10 year risk of coronary heart disease was
30% and whose total cholesterol
concentration was
5 mmol/l, four (3%) were taking lipid lowering
drugs. Of 385 adults aged 16-75 with a history of coronary heart
disease and eligible for lipid lowering treatment, 114 (30%;
25% to 34%) were taking lipid lowering drugs, of whom only 50 (44%; 35% to 53%) had a total cholesterol concentration <5
mmol/l.
Conclusions:
Despite the high prevalence of
dyslipidaemia in English adults, the proportion of adults taking lipid
lowering drugs in 1998 was only 2.2%. Rates of treatment were low
among high risk patients eligible for primary prevention with lipid lowering drugs, and less than one third of patients with established cardiovascular disease received such treatment.
![]()
Introduction
Top
Abstract
Introduction
Methods
Results
Discussion
References
![]()
Methods
Top
Abstract
Introduction
Methods
Results
Discussion
References
30%. We applied the
Framingham risk equation to estimate 10 year risk of coronary heart
disease.17 This equation, which has been shown to be
acceptably accurate in northern European countries,18
includes participants' age, sex, smoking status, systolic blood
pressure, and total cholesterol and HDL cholesterol concentrations, and
whether they have diabetes. The equation was applied to people aged
30-70, the range for which risk assessment in primary prevention is
recommended and above which evidence from trials of lipid lowering
drugs is required.
![]()
Results
Top
Abstract
Introduction
Methods
Results
Discussion
References
16 years) were
visited by a nurse, of whom 294 (2.2%) reported taking lipid lowering
drugs and 10 569 (77.8%) had a valid cholesterol measurement taken. Our analyses relate to these 10 569 participants (5001 men, mean age
47.8 (SE 0.25); 5568 women, mean age 48.5 (SE 0.24)).
7.8 mmol/l, 22.1% (21.3% to 22.9%)
6.5mmol/l, and 67.5% (66.6% to 68.4%)
5 mmol/l (table 2).
Among men the highest proportions above all three cut-off
concentrations were in participants aged 45-64, whereas among women the
highest proportions were found in those aged
65. Similarly, the
proportion of participants with a ratio of total cholesterol to HDL
cholesterol ratio of 5 or above, including participants taking lipid
lowering drugs, increased with age only among women, and the ratio was
always higher among men than women. Overall 237 (2.2%; 1.9% to 2.5%)
adults reported taking lipid lowering drugs; the relation between use
of lipid lowering drugs and age reflected that between adverse lipid
concentrations and age.
Of the 2335 participants with either a total cholesterol
concentration
6.5 mmol/l or taking lipid lowering drugs, 13%
of the 1004 men and 8% of the 1331 women were taking lipid lowering drugs, with only 4% of men and 2% of women having their total cholesterol "controlled" to <5 mmol/l (table 3).
Hence 35% of men and 20% of women taking treatment
reached this currently recommended target. Rates of treatment and
control were highest in participants aged 45-64. Of the 2804 participants with either a ratio of total cholesterol to HDL
cholesterol
5 or taking lipid lowering drugs, 7% of the 1769 men
and 11% of the 1035 women were taking lipid lowering drugs, and 4% of
the men and 8% of the women had their total to HDL cholesterol ratio
"controlled" to <5. Hence 57% of men taking treatment and 71% of
women taking treatment had their ratio adequately
"controlled."
|
Of the 7098 participants aged 30-70 who reported no history of coronary
heart disease or stroke, 6304 (2895 men and 3409 women) provided
sufficient data for a 10 year risk of coronary heart disease to be
calculated. Of these, 110 men (3.8%) and 12 women (0.4%) had a 10 year risk
30%. Of these 122 men and women, two men and two women
were taking lipid lowering drugs, none of whom had their total
cholesterol concentration lowered to <5 mmol/l. Of the 118 untreated
adults only five (4%) had a total cholesterol concentration <5
mmol/l.
Of all the participants aged 16-75 (no evidence from statin trials is available for people aged over 75), 440 reported a history of coronary heart disease (table 4). Of these, 315 (72%) reported ever having had their cholesterol measured and 385 (88%) had a total cholesterol concentration >5 mmol/l or were taking treatment. Of these 385, 114 (30%; 95% confidence interval 25% to 34%) were taking treatment. Control rates (total cholesterol <5 mmol/l) were 15% in men and 9% in women. Hence, of the participants taking treatment 44% had a total cholesterol <5 mmol/l and 62% had their ratio of total to HDL cholesterol "controlled" to <5. Rates of treatment and control were highest among people aged 45-64.
|
Of the participants aged >75, 180 reported a history of coronary heart
disease, of whom 143 (79%) had a total cholesterol concentration above
5 mmol/l or were on lipid lowering drugs. Of these 143, nine (6%) were
taking treatment and two (1%) had a total cholesterol concentration
<5 mmol/l.
| |
Discussion |
|---|
|
|
|---|
In this large, nationally representative sample, about two
thirds of participants had a total cholesterol concentration above the
"ideal" of 5 mmol/l, and despite the high prevalence of coronary heart disease in the English population3 only 2% were
taking lipid lowering agents. Thresholds and targets for the use of
lipid lowering drugs evaluated in this report reflect early guidelines that recommended the use of lipid lowering drugs for primary prevention at various thresholds of total cholesterol, including 6.5 mmol/l and
7.8 mmol/l,
19 20
as well as more recent guidelines that recommend intervention on the basis of estimated absolute coronary risk.
11 12
Recent guidelines in the United Kingdom for
primary prevention recommend the use of statins in people whose
estimated 10 year risk of coronary heart disease is
30%, and
treatment targets in the United Kingdom include a total cholesterol
concentration of <5 mmol/l.
Overall, only about 10% of adults with dyslipidaemia (total
cholesterol
6.5 mmol/l or taking lipid lowering drugs) received lipid lowering treatment, and cholesterol concentrations were reduced
to the current target of <5 mmol/l in less than one third of people
undergoing treatment. Defining dyslipidaemia as a ratio of total to HDL
cholesterol >5 gives a treatment rate of only one person in 12, but
most people treated had their ratio reduced to <5.
The low rate of lipid lowering treatment in people reporting a history
of coronary heart disease is also worrisome. Less than one third of
this group
for which lipid lowering drugs are
recommended
were taking them, and total cholesterol
concentrations were reduced to current targets in only about one in
eight eligible participants. We estimate, on the basis of changes in
lipid concentrations and effects on outcomes reported in recent
trials,
6 9 10
that if an equivalent amount of lipid
lowering was achieved in the 70% of untreated adults aged 16-75 in
England with a history of coronary heart disease and eligible for such
treatment,
12 16
about 7000 fatal or non-fatal myocardial
infarctions and about 2500 fatal or non-fatal strokes would be avoided
each year.
People who are eligible for primary prevention with lipid lowering
treatment, on the basis of a 10 year risk of coronary heart disease of
30%, cannot be identified from these data because treatment with
lipid lowering drugs means that the proportion of people above this
risk level before treatment started is underestimated. Furthermore, we
cannot evaluate whether the use of lipid lowering drugs by those whose
risk of coronary heart disease risk was <30% during treatment was
appropriate on the basis of current recommendations. Nevertheless, of
the 117 participants whose 10 year risk of coronary heart disease was
estimated at
30% and whose total cholesterol concentration was
5
mmol/l, only four were taking lipid lowering drugs, and none of these
had achieved a total cholesterol of <5 mmol/l.
Given the huge beneficial effects of statins on cardiovascular events in both primary 7 8 and secondary 6 9 10 prevention, it is hard to explain why the observed rates of treatment were so low. Undoubtedly, early misplaced concern about possible adverse effects of lipid lowering agents5 has contributed. Although lipid data in this survey were based on single non-fasting concentrations rather than repeated measures taken before starting treatment, this is unlikely to have exaggerated the apparent low rates of treatment. Although the use of lipid lowering agents is low, and much lower than recommended both before and during 1998, 11 12 19 the rate of treatment as monitored in the health survey for England had risen from 0.4% in 1994 to 2.2% in 1998.
We hope that the recently established national service framework16 will reinforce national and international guidelines on lipid management, so that further growth in the use of statins continues and the massive benefits in terms of preventing cardiovascular events can be realised.
|
What is already known on this topic
Dyslipidaemia is a major risk factor for coronary heart disease, which is a major cause of mortality in the United Kingdom and Ireland Five trials since 1994 have shown that statins in both primary and secondary prevention have major benefits for preventing cardiovascular events What this study addsAt least a quarter of English adults have adverse lipid profiles Only 1 in 50 English adults uses a lipid lowering agent (30% of people
with a history of cardiovascular disease and 3% of people with a 10 year risk of coronary heart disease of The total cholesterol concentration is reduced to the currently recommended targets in only a minority of patients being treated with lipid lowering drugs |
| |
Acknowledgments |
|---|
The 1998 health survey for England was carried out by the Joint Health Survey Unit of the National Centre for Social Research (formerly SCPR) and the Department of Epidemiology and Public Health at University College London.
Contributors: NP planned the analyses and PP, who is the survey doctor for the health survey for England, advised on and carried out the analyses. NP and PP wrote the report and will act as guarantors for the study.
| |
Footnotes |
|---|
Funding: PP receives funding from the Department of Health to carry out the health survey for England.
Competing interests: None declared.
| |
References |
|---|
|
|
|---|
| 1. | World Health Organization. World health statistics annual 1996. Geneva: WHO, 1998. |
| 2. | Erens B, Primatesta P, eds. Health survey for England. Cardiovascular disease '98. , Vol 1. Findings London: Stationery Office, 1999. |
| 3. | British Heart Foundation Health Promotion Research Group. European cardiovascular disease statistics. London: BHF, 2000. |
| 4. | Ravnskov U. Cholesterol lowering trials in coronary heart disease: frequency of citation and outcome. BMJ 1992; 305: 15-19. |
| 5. | Oliver MF. Might treatment of hypercholesterolaemia increase non-cardiac mortality? Lancet 1991; 337: 1529-1531[CrossRef][Medline]. |
| 6. | 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]. |
| 7. |
Shepherd J, Cobbe SM, Ford I, Isles CG, Lorimer AR, MacFarlane PW, et al.
Prevention of coronary heart disease with pravastatin in men with hypercholesterolaemia.
N Engl J Med
1995;
333:
1301-1307 |
| 8. | 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; 79: 1615-1622. |
| 9. |
Sacks FM, Pfeffer MA, Moye LA, Rouleau JL, Rutherford JD, Cole TG, 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 |
| 10. |
Long Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group.
Prevention of cardivascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels.
New Engl J Med
1998;
339:
1349-1357 |
| 11. | NHS Executive. Standing medical advisory committee on use of statins. London: Department of Health, 1997. |
| 12. |
Wood D, Durrington P, Poulter N, McInnes G, Rees A, Wray R, for the British Cardiac Society, British Hyperlipidaemia Association, British Hypertension Society, and British Diabetic Association.
Joint British recommendations on prevention of coronary heart disease in clinical practice.
Heart
1998;
80:
S1-29 |
| 13. |
Rubins HB, Robins SJ, Collins D, Fye CL, Anderson JW, Elam MB, et al.
Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol.
N Engl J Med
1999;
341:
410-418 |
| 14. | Erens B, Primatesta P, eds. Health survey for England. Cardiovascular disease '98. , Vol 2. Methodology and documentation London: Stationery Office, 1999. |
| 15. |
Siedel J, Hagele EO, Ziegenhorn J, Wahlfeld AW.
Reagents for the enzymatic determination of serum total cholesterol with improved lipolytic effect.
Clin Chem
1983;
29:
1075-1080 |
| 16. | National Service Framework for Coronary Heart Disease. Modern standards and service models, 2000. London: Stationery Office, 2000. |
| 17. | Anderson KM, Odell PM, Wilson PWP, Kannel WB. Cardiovascular disease risk profiles. Am Heart J 1991; 121: 293-298[CrossRef][Medline]. |
| 18. |
Haq IU, Ramsay LE, Yeo WW, Jackson PR, Wallis EJ.
Is the Framingham risk function valid for northern European populations? A comparison of methods for estimating absolute coronary risk in high risk men.
Heart
1999;
81:
40-46 |
| 19. |
Betteridge DJ, Dodson PM, Durrington PN, Hughes EA, Laker MF, Nicholls DP, et al.
Management of hyperlipidaemia: guidelines of the British Hyperlipidaemia Association.
Postgrad Med J
1993;
69:
359-369 |
| 20. |
Expert Panel.
Report of the national cholesterol education program expert panel on detection, evaluation, and treatment of high blood cholesterol in adults.
Arch Intern Med
1988;
148:
36-69 |
(Accepted 26 September 2000)
Read all Rapid Responses