(Stroke. 2000;31:1882.)
© 2000 American Heart Association, Inc.
Original Contributions |
From the Department of Primary Care and Population Sciences (S.G.W., A.G.S.), Royal Free and University College Medical School, and the Department of Social Medicine (S.E.), University of Bristol, Canynge Hall, Bristol, UK.
Correspondence to Dr S. Goya Wannamethee, Department of Primary Care and Population Sciences, Royal Free and University College Medical School, Rowland Hill St, London NW3 2PF, UK. E-mail goya{at}rfhsm.ac.uk
| Abstract |
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MethodsWe carried out a prospective study in 7735 men, 40 to 59 years of age, drawn from 1 group practice in each of 24 British towns. Men with history of stroke were excluded (n=52).
ResultsDuring the mean follow-up period of 16.8 years, there
were 343 stroke cases (fatal and nonfatal) in the 7683 men with no
history of stroke. Higher levels of HDL cholesterol were
associated with a significant decrease in risk of stroke even after
adjustment for potential confounders (top fifth versus lowest fifth:
adjusted relative risk=0.68, 95% CI 0.46 to 0.99). The inverse
relation was seen only for nonfatal strokes (adjusted relative
risk=0.59, 95% CI 0.39 to 0.90; top fifth versus lowest fifth). Total
cholesterol showed no graded association with fatal
strokes, but men with levels
8.1 mmol/L (top 5% of the
distribution) showed increased risk of nonfatal stroke, although this
was not statistically significant after adjustment (adjusted RR=1.46,
95% CI 0.91 to 2.32). The beneficial effects of elevated HDL
cholesterol on nonfatal stroke were seen in both smokers
and nonsmokers and were more evident in men with hypertension than in
normotensives. In hypertensive men, elevated HDL
cholesterol (top fifth) was associated with a significant
50% reduction in risk of nonfatal strokes compared with men in the
lowest fifth.
ConclusionsHigher levels of HDL cholesterol were associated with a significant decrease in risk of nonfatal stroke. In contrast, elevated total cholesterol showed a weak positive association with nonfatal strokes. The marked inverse association between HDL cholesterol and stroke seen in hypertensives emphasizes the importance of those modifiable risk factors for stroke known to lower the concentrations of HDL cholesterol.
Key Words: cholesterol lipoproteins, HDL cholesterol stroke
| Introduction |
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| Subjects and Methods |
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160 mm Hg or
diastolic blood pressure
90 mm Hg or receiving
antihypertensive treatment. Details of classification methods for
smoking status, alcohol consumption, social class (longest held
occupation), and physical activity have been
reported.8 12 13 The men were classified according to
their current cigarette smoking status into 6 groups: those who had
never smoked cigarettes, excigarette smokers, and 4 groups of current
cigarette smokers (1 to 19, 20, 21 to 39, and
40 cigarettes/d). Heavy
drinking is defined as drinking >6 units (1 UK unit=8 to 10 g
alcohol) daily or on most days in the week. A physical activity score
was derived for each man on the basis of frequency and type of leisure
activity, and the men were grouped into 6 broad categories on the basis
of their total score: inactive, occasional, light, moderate, moderately
vigorous, and vigorous.13 "Active men" were those
graded "moderate or more active."
Preexisting Disease
The men were asked whether a doctor had ever told them that they
had angina or myocardial infarction (heart attack, coronary
thrombosis), stroke, diabetes, and a number of other disorders. They
were also asked for details of any regular medical treatment including
antihypertensive treatment. The World Health Organization (Rose) chest
pain questionnaire14 was administered to all men at the
initial examination, and a 3-orthogonal-lead ECG was recorded at
rest.
Previous Stroke
Evidence of a previous stroke was determined by the subjects
recall of such a diagnosis made by a physician (n=52 men), and these
men have been excluded from the analyses.
Coronary Heart Disease
Men with evidence of coronary heart disease (CHD) were
defined as those with recall of a diagnosis of angina or heart attack
made by a physician, those with angina or a possible myocardial
infarction on World Health Organization (Rose) chest pain
questionnaire,14 or with ECG evidence of possible or
definite myocardial ischemia or myocardial infarction.
Diabetes
History of diabetes was based on recall of a physicians
diagnosis.
Lipid-Lowering Drugs
Only 35 men were taking lipid-lowering drugs at screening, and
they are included in the overall analyses.
Follow-Up
All men irrespective of previous CHD or stroke events were
followed up for all-cause mortality and for
cardiovascular morbidity.16 All
cardiovascular events occurring in the period up to
December 1995 are included in the study, an average follow-up of 16.8
years (range 15.5 to 18.0 years), and follow-up has been achieved for
99% of the cohort. Information on death was collected through the
established "tagging" procedures provided by the National Health
Service registers in Southport (England and Wales) and Edinburgh
(Scotland). Fatal stroke episodes were those coded on the death
certificate to International Classification of Diseases codes 430 to
438. Nonfatal stroke events were those which produced a neurological
deficit that was present for >24 hours. Fatal stroke events in
this report include only those deaths that occurred as the first event
in the course of follow-up and not deaths that were preceded by a
nonfatal event. Analyses separate stroke into fatal and
nonfatal events on the assumption that fatal first strokes are more
severe and are likely to be due to hemorrhage. Evidence
regarding strokes was obtained by reports from general
practitioners, by biennial reviews of the patients notes
through to the end of the study period, and from personal
questionnaires to surviving subjects at the 5th year and 12th year
after initial examination. All death certificates in which it appeared
that coding to stroke was not appropriate or in which stroke was not
the attributed code when it might have been were explored by
correspondence with the certifying physician and the hospital
concerned. No information on the type of stroke was available.
Statistical Methods
The Cox proportional hazards model was used to assess the
independent contributions of HDL cholesterol and total
cholesterol to the risk of stroke and CHD and to obtain the
relative risks (RRs) adjusted for age and the other risk
factors.17 The men were divided into 5 groups of
approximately equal numbers based on the distributions for HDL
cholesterol and total cholesterol. Because of
the suggestion that risk of stroke may only be elevated at the upper
extreme tail of the total cholesterol
distribution,6 men in the upper fifth of distribution were
further separated, and 6 groups are used. The distribution of
triglycerides was skewed and log transformation was used.
In the adjustment, age, systolic blood pressure and body mass
index (BMI) were fitted as continuous variables. Smoking (6
levels), physical activity (6 levels), diabetes (yes/no), preexisting
stroke (yes/no), use of antihypertensive treatment (yes/no), and
preexisting CHD on questionnaire/ECG (3 levels) were fitted as
categorical variables. Direct standardization was used to obtain
age-adjusted rates per 1000 person-years with 5-year age intervals and
the study population as the standard. To assess whether the relation
between HDL cholesterol and stroke differed by risk factor
status, interaction terms with the HDL cholesterol groups
fitted continuously were used.
| Results |
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Blood Lipids and Risk of Total Stroke
HDL Cholesterol
Risk of stroke decreased significantly with increasing levels of
HDL cholesterol after adjustment for age (test for trend
P=0.005) (Table 2
). In this
cohort, HDL cholesterol concentrations have been shown to
be associated with wide range of cardiovascular risk
factors.9 18 Further adjustment for potential
confounders viz cigarette smoking, physical activity, alcohol intake,
BMI, preexisting CHD, diabetes, antihypertensive treatment, and
systolic blood pressure increased the RR and reduced the trend,
but it remained significant (P=0.03). There was little
difference among the lower 3 quintiles, but men in the highest fifth of
HDL cholesterol concentration still showed significantly
lower risk than those in the lowest fifth.
|
Total Cholesterol
Risk of stroke was only significantly increased among men in the
top 5% of the distribution after adjustment for age (Table 2
).
Further adjustment for confounders considerably reduced the increased
risk, which was no longer statistically significant.
HDL Cholesterol/Total Cholesterol Ratio
A weak inverse association was seen between the HDL
cholesterol/total cholesterol ratio and risk of
stroke after adjustment. The adjusted RRs for the 5 quintiles of the
distribution were 1.00, 0.91 (0.66, 1.27), 1.02 (0.73, 1.43), 0.78
(0.54, 1.11), and 0.81 (0.56, 1.18).
Serum Triglycerides
No association was seen between triglycerides and risk
of total stroke (data not shown).
Fatal and Nonfatal Stroke
Subjects with fatal stroke (Table 1
) were older, had higher
systolic and diastolic blood pressures, and were
far more likely to be receiving treatment for hypertension than those
with nonfatal stroke. They were more likely to be heavy drinkers and
thus, not surprisingly, had higher HDL cholesterol
concentrations than nonfatal stroke subjects. The relations between HDL
cholesterol and stroke and serum total
cholesterol and stroke were examined separately for fatal
and nonfatal strokes (Table 3
). An
inverse association with HDL cholesterol was seen with
nonfatal strokes after adjustment, with lower risk from the fourth
quintile (test for trend P=0.03). Men in the highest fifth
showed significantly lower risk of nonfatal stroke than men in the
lowest fifth. No association was seen with fatal strokes. The relations
observed were similar in the first 8 years of follow-up and in the
second 8-year period. When the analysis in Table 3
was
restricted to the 196 cases in which triglycerides were
available, the results were unchanged. Total cholesterol
showed no association with fatal strokes, but men in the top 5% of the
distribution showed increased risk of nonfatal strokes, although this
was not of statistical significance after full adjustment. The HDL
cholesterol/total cholesterol ratio showed a
weak and nonsignificant inverse association with nonfatal strokes
(adjusted RR=1.00, 0.91, 1.08, 0.74, and 0.80 for the 5 quintiles,
respectively). No association was seen between serum
triglycerides and nonfatal stroke.
|
HDL Cholesterol and Stroke by Levels of Risk
Factors
Because of the strong relation between stroke and risk factors
such as hypertension, cigarette smoking, and preexisting
CHD,19 we have examined the effects of serum HDL
cholesterol on nonfatal stroke by the degree of risk
associated with these factors. The Figure
shows the age-adjusted nonfatal rates per 1000 person-years and Table 4
shows the RRs adjusted for age,
physical activity, alcohol intake, BMI, diabetes, smoking,
systolic blood pressure, and preexisting CHD by levels of these
factors. Because of the smaller number involved when stratifying, we
are primarily concerned with whether the associations differ between
the levels of these factors rather than the statistical significance
within each subgroup. Higher levels of serum HDL
cholesterol were associated with reduced risk of nonfatal
stroke in both normotensives and hypertensives, although the reduction
was more marked in hypertensives. A test for interaction to see whether
the relation between HDL cholesterol and nonfatal strokes
differed by hypertension status was not statistically significant
(P=0.09). The inverse relation was seen in both smokers and
nonsmokers and in men both with and without preexisting CHD, although
the inverse trend was more apparent in those with CHD. However, tests
for interaction showed no significant interaction between HDL
cholesterol and smoking status or preexisting CHD
(P=0.50 and P=0.41, respectively).
|
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BMI, HDL Cholesterol, and Stroke
Because of the strong influence that BMI has on HDL
cholesterol,20 we examined the relation
between HDL cholesterol and risk of stroke in men with BMI
levels <25 and those with levels
25, generally regarded to be
overweight (Figure
[fig+1] and Table 4
). An inverse association
was seen in both groups of men after adjustment for age, although the
inverse relation was more marked in leaner men. After further
adjustment for potential confounders, the inverse association was only
seen in lean men, and a test for interaction was significant
(P=0.04). Further exploration of the findings in the
25
kg/m2 group indicate that men in the 25 to 27.9
kg/m2 subgroup behaved similarly to the men in
the <25 kg/m2 group. Those with BMI
28
kg/m2 show an increased risk of stroke in men in
the highest HDL cholesterol category. This group of obese
men with high HDL cholesterol had a particularly high
proportion of heavy drinkers (25%).
| Discussion |
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Blood Cholesterol and Stroke
The role of blood cholesterol in stroke prevention is
unclear. Most prospective studies have failed to find a relation
between total cholesterol and risk of total
stroke.22 It has been proposed that this may be due to the
differing association with subtypes of stroke.23 An
inverse association has been observed with hemorrhagic
strokes24 and a positive association with ischemic
stroke.24 25 However, not all observational studies have
found a positive association between total cholesterol and
ischemic stroke.25 We observed little relation
between total cholesterol and nonfatal strokes except at
the extreme end of the distribution. Risk of stroke was increased only
in men with levels
8.1 mmol/L (top 5%), although this was not
statistically significant after adjustment. This finding is
consistent with the findings from the Copenhagen
Study.6 Despite the lack of association between serum
total cholesterol and risk of stroke in observational
epidemiological studies, the results of lipid-lowering trials with
statin agents suggest benefit for stroke reduction.26 27 28
It has been suggested that the beneficial effects of statins on
clinical events may involve mechanisms independent of lipid-lowering
such as modification of endothelial function,
inflammatory responses, plaque stability, and thrombus
formation.29
Clinical Implications
HDL cholesterol is inversely associated with risk of
nonfatal stroke (presumably ischemic), and this relation was
observed in both smokers and smokers and was more apparent in lean men
and in men with preexisting CHD and was particularly striking in
hypertensive men. The lack of protective effect in the heavier men
(
25 kg/m2) may be explained by the high
proportion of heavy drinkers with high HDL cholesterol and
obesity, who are likely to have an increased risk of stroke. In
hypertensives, elevated HDL cholesterol was associated with
a 50% reduction in the risk of nonfatal strokes. Because these men are
at very high absolute risk of stroke, the absolute benefits of high HDL
cholesterol are large. Our findings also suggest that
caution should be taken in using ß-blockers in hypertensive men
because these drugs tend to lower HDL cholesterol by up to
10% and to raise triglycerides by up to
30%.30 ß-Blockers, unlike thiazides, did not show any
significant effect on stroke risk in the MRC mild hypertension
trial,31 and it may be that their lack of effect was due
to their effect on HDL cholesterol.
HDL cholesterol is recognized as one of the factors adversely influencing prognosis in hypertensive subjects, although it is not currently used for risk stratification.32 Our findings confirm that HDL cholesterol is an independent risk factor for nonfatal stroke, and it remains to be determined whether its inclusion in overall stroke risk assessment is of any value. HDL cholesterol is lowered by many adverse lifestyle factors associated with cardiovascular disease, in particular smoking and overweight and or obesity. Our findings emphasize the importance of modifying these lifestyle factors in the management of hypertension.
| Acknowledgments |
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Received December 17, 1999; revision received April 17, 2000; accepted May 5, 2000.
| References |
|---|
|
|
|---|
2. Qizilbash N, Jones L, Warlow C, Mann J. Fibrinogen and lipid concentrations as risk factors for transient ischaemic attacks and minor ischaemic strokes. BMJ. 1991;303:605609.
3. Sridharan R. Risk factors for ischaemic stroke: a case control analysis. Neuroepidemiology. 1992;11:2430.[Medline] [Order article via Infotrieve]
4. Bihari-Varga M, Szekely J, Gruber E. Plasma high density lipoproteins in coronary, cerebral and peripheral vascular disease: the influence of various risk factors. Atherosclerosis. 1981;40:337345.[Medline] [Order article via Infotrieve]
5.
Gordon T, Kanel WB, Castelli WP, Dawber TR.
Lipoproteins, cardiovascular disease and death: the
Framingham Study. Arch Intern Med. 1981;141:11281131.
6.
Lindenstrom E, Boysen G, Nyboe J. Influence
of total cholesterol, high density lipoprotein
cholesterol and triglycerides on risk of
cerebrovascular disease: the Copenhagen City heart Study.
BMJ. 1994;309:1115.
7.
Tanne D, Yaari S, Goldbourt U. High-density
lipoprotein cholesterol and risk of ischaemic stroke
mortality: a 21-year follow-up of 8586 men from the Israeli Ischaemic
Heart Disease Study. Stroke. 1997;28:8387.
8. Shaper AG, Pocock SJ, Walker M, Cohen NM, Wale CJ, Thomson AG. British Regional Heart Study: cardiovascular risk factors in middle-aged men in 24 towns. Br Med J. 1981;283:179186.
9.
Thelle DS, Shaper AG, Whitehead TP, Bullock DG,
Ashby D, Patel I. Blood lipids in middle-aged British men. Br
Heart J. 1983;49:205213.
10.
Pocock SJ, Ashby D, Shaper AG, Walker M,
Broughton PM. Diurnal variations in serum biochemical and
haematological measurements. J Clin Pathol. 1989;42:172179.
11. Bruce NG, Shaper AG, Walker M, Wannamethee G. Observer bias in blood pressure studies. J Hypertens. 1988;6:374380.
12. Shaper AG, Wannamethee G, Walker M. Alcohol and mortality: explaining the U-shaped curve. Lancet. 1988;2:12681273.
13.
Shaper AG, Wannamethee G, Weatherall R. Physical
activity and ischaemic heart disease in middle-aged men. Br
Heart J. 1991;66:384394.
14.
Cook DG, Shaper AG, Macfarlane PW. Using the WHO
(Rose) angina questionnaire in cardiovascular
epidemiology studies. Int J
Epidemiol. 1989;18:607613.
16. Walker M, Shaper AG. Follow-up of subjects in prospective studies based in general practice. J R Coll Gen Pract. 1984;34:365370.[Medline] [Order article via Infotrieve]
17. Cox DR. Regression models and life tables (with discussion) J R Stat Soc B. 1972;34:187220.
18.
Wannamethee G, Shaper AG. Blood lipids: the
relationship with alcohol intake, smoking and body weight. J
Epidemiol Community Health. 1992;46:197202.
19. Shaper AG, Phillips AN, Pocock SJ, Walker M, Macfarlane PW. Risk factors for stroke in middle-aged British men. BMJ. 1991;302:11111115.
20. Wannamethee SG, Shaper AG, Durrington P, Perry I. Hypertension, serum insulin, obesity and the metabolic syndrome. J Hum Hypertens. 1998;12:735741.[Medline] [Order article via Infotrieve]
21. Sandercock PAG, Warlow CP, Jones LN, Starkey IR. Predisposing factors for cerebral infarction: the Oxfordshire Community Stroke Project. BMJ. 1989;298:7580.
22. Prospective Studies Collaboration. Cholesterol, diastolic blood pressure and stroke: 13000 stroke in 450000 people in 45 prospective cohorts. Lancet. 1995;346:16471653.[Medline] [Order article via Infotrieve]
23. Iso H, Jacobs DE, Wentworth D, Neaton JD, Cohen JD. Serum cholesterol levels and six year mortality from stroke in 350,977 men screened for the Multiple Risk Factor Intervention Trial. N Engl J Med. 1989;320:904910.[Abstract]
24. Benfante R, Yano K, Hwang LJ, Curb JD, Kagan A, Ross W. Elevated serum cholesterol is a risk factor for both coronary heart disease and thromboembolic stroke in Hawaiian Japanese men: implications of shared risk. Stroke. 1994;25:814820.[Abstract]
25. Gorelick PB, Mazzone T. Plasma lipids and stroke. J Cardiovasc Risk. 1999;6:217221.[Medline] [Order article via Infotrieve]
26.
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;278:313321.
27.
Plehn JF, Davis BR, Sacks FM, Rouleau JL, Pfeffer
MA, Bernstein V, Cuddy E, Moye LA, Piller LB, Rutherford J, Simpson LM,
Braunwald E; for the CARE Investigators. Reduction of stroke incidence
after myocardial infarction with pravastatin: the
Cholesterol and Recurrent Events (CARE) Study.
Circulation. 1999;99:216223.
28.
Bucher HC, Griffith LE, Guyatt GH. Systematic
review on the risk and benefit of different
cholesterol-lowering interventions. Arterioscler
Thromb Vasc Biol. 1999;19:187195.
29.
Rosenson RS, Tangney CC. Antiatherothrombotic
properties of statins: implications for cardiovascular
event reduction. JAMA. 1998;279:16431650.
30. Evans K, Laker MF. Intra-individual factors affecting lipid, lipoprotein and apolipoprotein measurement: a review. Ann Clin Biochem. 1995;32:261280.
31. Medical Research Council Working Party. MRC trial of treatment of mild hypertension: principal results. BMJ. 1985;291:97104.
32. Guidelines Subcommittee. World Health Organisation-International Society of Hypertension guidelines for the management of hypertension. J Hypertens. 1999;1999:17:151183.
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H. Bloomfield Rubins, J. Davenport, V. Babikian, L. M. Brass, D. Collins, L. Wexler, S. Wagner, V. Papademetriou, G. Rutan, and S. J. Robins Reduction in Stroke With Gemfibrozil in Men With Coronary Heart Disease and Low HDL Cholesterol : The Veterans Affairs HDL Intervention Trial (VA-HIT) Circulation, June 12, 2001; 103(23): 2828 - 2833. [Abstract] [Full Text] [PDF] |
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