Research paper Blacks managing high blood pressure while maintaining a quality lifestyle
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Racial Disparity in Hypertension Control:
Tallying the Death Toll
ABSTRACT PURPOSE Black Americans with hypertension have poorer blood pressure control than their white counterparts, but the impact of this disparity on mortality among black adults is not known. We assessed differences in systolic blood pressure (SBP) control among white and black adults with a diagnosis of hypertension, and mea- sured the impact of that difference on cardiovascular and cerebrovascular mortality among blacks.
METHODS Using SBP measurements from white and black adults participating in the National Health and Nutrition Examination Survey, 1999-2002, we modeled changes in mortality rates resulting from a reduction of mean SBP among blacks to that of whites. Our data source for mortality estimates of blacks with hyper- tension was a meta-analysis of observational studies of SBP; our data source for reduction in mortality rates was a meta-analysis of SBP treatment trials.
RESULTS The fi nal sample of participants for whom SBP measurements were available included 1,545 black adults and 1,335 white adults. The mean SBP among blacks with hypertension was approximately 6 mm Hg higher than that for the total adult black population and 7 mm Hg higher than that for whites with hypertension. Within the hypertensive population, a reduction in mean SBP among blacks to that of whites would reduce the annual number of deaths among blacks from heart disease by 5,480 and from stroke by 2,190.
CONCLUSIONS Eliminating racial disparity in blood pressure control among adults with hypertension would substantially reduce the number of deaths among blacks from both heart disease and stroke. Primary care clinicians should be particularly diligent when managing hypertension in black patients.
Ann Fam Med 2008;6:497-502. DOI: 10.1370/afm.873.
INTRODUCTION
C ardiovascular disease, the leading cause of death in the United
States, occurs at the highest rate among black Americans.1 As a
precursor to cardiovascular disease, hypertension is one of the
most important contributors to racial disparities in mortality rate.2 The
age-adjusted prevalence of hypertension is signifi cantly higher among
blacks (39%) than among whites (29%).3 Uncontrolled hypertension has
an enormous impact on the health of minorities,1,4 accounting for up to
one-quarter of all deaths among black adults, primarily from cardiovascu-
lar and cerebrovascular causes.5
Recent data suggest that among persons under treatment for hyperten-
sion, blacks have poorer blood pressure control.3 Only a few studies have
quantifi ed the effects of racial disparities in health care interventions on
the number of deaths among.6,7 To our knowledge, none have quantifi ed
the impact of disparity in hypertension control on black mortality.
To model the impact of this disparity in hypertension control, we
used national data on systolic blood pressure (SBP), mortality data, and
published estimates of the relative risk associated with decreases in SBP.
Specifi cally, we calculated the annual numbers of heart and stroke deaths
Kevin Fiscella, MD, MPH1,2
Kathleen Holt, PhD1
1Department of Family Medicine, Univer-
sity of Rochester School of Medicine and
Dentistry, Rochester, New York
2Department of Community and Preven-
tive Medicine, University of Rochester
School of Medicine and Dentistry, Roch-
ester, New York
Confl icts of interest: none reported
CORRESPONDING AUTHOR
Kevin Fiscella, MD, MPH
Departments of Family Medicine,
and Community and Preventive Medicine
University of Rochester School
of Medicine and Dentistry
1381 South Ave
Rochester, NY 14620
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that would be avoided or postponed assuming blacks
with hypertension had their blood pressure controlled
to the same level as whites.
METHODS Data Sources We used SBP data from the National Health and
Nutrition Examination Survey (NHANES) for the
years 1999-2002. NHANES is a periodic national
survey of the health status of the United States and is
designed to yield nationally representative estimates.
It includes data from questionnaires, physical examina-
tions, and medical tests. Eligibility criteria for our sam-
ple included (1) self-identifi cation as white or black, (2)
age of 25 years or older, and (3) diagnosis of hyperten-
sion (regardless if treated or not). We also used 2002
US black mortality data for heart disease and stroke,
stratifi ed by sex and age.8
We estimated the additional risk associated with
an elevated SBP based on a meta-analysis of epidemio-
logic studies of SBP and mortality. This meta-analysis,
based on approximately 1 million individuals, estimated
the risks, stratifi ed by age and sex, of heart disease
and stroke associated with elevated blood pressure.9
We estimated the effect of reductions in SBP based
on relative risks for heart disease and stroke mortality
from a meta-analysis of randomized treatment trials of
hypertension.10
Estimating Black Mortality Risk From Hypertension National mortality rates are known for all black adults
(ie, those with and without hypertension), but not for
black adults with hypertension. To estimate sex- and
age- specifi c mortality rates for this group, we used
NHANES data to derive the mean difference in SBP
between blacks with hypertension and all blacks by sex
and age. Next, we calculated the relative risk associ-
ated with a given difference in SBP between blacks
with hypertension and all blacks using the following
sex- and age-specifi c exponential function, derived
from a meta-analysis of observational studies of blood
pressure and mortality9:
RR = RRs (ΔSBP/20)
where ΔSBP equals the difference in mean SBP
between blacks with a hypertension diagnosis and
all blacks aged 25 years or older, and RRs equals the
relative risk for heart disease or stroke by age and sex
for a standardized ΔSBP of 20 mm Hg. The relative
risk was then applied to each sex and age category for
heart disease and stroke mortality to produce mortality
rates adjusted for hypertension. For example, the dif-
ference in mean SBP among black men aged 55 to 64
years with hypertension relative to all black men in this
age category was 5 mm Hg (142 vs 137 mm Hg). This
difference represents a relative risk for heart disease
mortality of 1.17 (1/0.53 (5/20)). The overall mortality
rate for black men in this age-group is 605 deaths per
100,000. Among black men of this age with hyperten-
sion, the overall mortality is thus estimated at 708 per
100,000 (605 × 1.17). This estimate is conservative because it does not adjust for comorbidity (such as
diabetes, hyperlipidemia, or obesity) associated with
hypertension.11
Estimating Relative Risk From Disparity in SBP We estimated the relative risk associated with racial dis-
parity in SBP based on a reduction in the mean SBP for
blacks to that of whites in the same sex and age group.
We calculated the mean difference in SBP between
blacks and whites for each group using NHANES
data and used a relative risk for reduction in SBP from
a meta-analysis of randomized trials of hypertension
treatment.10 In that meta-analysis, an 8.3-mm Hg reduc-
tion in SBP was associated with a relative risk of 0.80
(95% confi dence interval [CI], 0.77-0.84) for heart
disease mortality and a relative risk of 0.67 (95% CI,
0.61-0.74) for stroke mortality. We then estimated the
relative risk in heart disease mortality for various reduc-
tions in SBP using the following formula:
RR = RRs Δ SBP/8.3
where ΔSBP equals the difference in SBP between
blacks and whites matched for sex and age based on
NHANES data, and RRs is the relative risk for heart
disease or stroke standardized to an 8.3-mm Hg
decrease in SBP. We then converted relative risks to
relative risk reductions (RRR = 1 – RR).
Estimating Deaths From Disparity in SBP To estimate the number of deaths among blacks that
would be postponed or avoided if parity in SBP control
were achieved, we multiplied the relative risk reduc-
tion by the sex- and age-specifi c mortality rates (AMR)
for blacks adjusted for SBP to obtain the absolute risk
reduction. We then multiplied this by the estimated
number of blacks (N) in each sex and age group,
derived from NHANES data. Our estimate for deaths
was thus equal to RRR × AMR × N.
Statistical Analyses The number of persons in each sex and age group and
mean SBPs for blacks and whites were derived from
NHANES data, weighted to yield national estimates
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using SAS (SAS Institute Inc, Cary, North Carolina).
All other calculations were performed using Microsoft
Excel (Microsoft Corp, Redmond, Washington).
Sensitivity Analyses We conducted a series of sensitivity analyses around
key estimates in the model. First, we assessed the effect
of assuming a ±30% black-white difference in SBP.
We also assumed a constant difference in SBP across
all age-groups using the mean SBP by sex to assess
the effect of age distributions on our fi ndings. Next,
we used the 95% CIs surrounding the estimated rela-
tives risks associated with decreases in SBP.10 Last, we
assumed comparable risk per change in SBP regardless
of the source of the estimate, for example, observa-
tional data vs treatment data.10
RESULTS There were 661 black adults and 1,335 white adults
with hypertension in the sample and an additional
884 blacks without hypertension. Table 1 shows the
number of black men and women in the sample with
hypertension in each age-group along with their mean
SBP and corresponding 95% CIs. For men, the mean
SBP was 22 mm Hg higher in the oldest as compared
with the youngest cohort. For women, that difference
was 26 mm Hg.
The differences in mean SBP by age and sex among
blacks with hypertension, the entire black adult popu-
lation, and non-Hispanic whites with hypertension are
shown in Table 2. The mean SBP among black men
with hypertension was 6 mm Hg higher than that for
all black men and 6.5 mm Hg higher than that for
white men with hypertension. For women, the differ-
ences were 6.5 and 8.2 mm Hg, respectively.
Table 3 shows the annual mortality rates by age
and sex for heart disease and stroke for the entire black
population, estimates of annual mortality rates for
those with hypertension, and estimates for blacks with
hypertension assuming racial parity in blood pressure
control. Parity in SBP control would reduce annual
mortality rates from heart disease and stroke among
men by 17% and 16%, respectively. For women, the
reductions would be smaller, 9% and 14%, respectively.
Racial parity in hypertension control would reduce
the annual number of deaths from heart disease and
stroke by an estimated 5,480 and 2,190 (Table 4). Sen-
sitivity analyses are shown in the Supplemental Appen-
dix (available online at http://www.annfammed.
org/cgi/content/full/6/6/497/DC1). Use of 30%
lower or higher estimates for racial differences in
SBP yielded a 23% to 28% variation in death estimates.
Use of a constant (mean SBP difference by race) across
age-groups yielded slightly lower estimates for men,
but substantially higher estimates for women relative to
the base case. In general, use of a constant difference
Table 1. Mean Systolic Blood Pressures of Blacks With Hypertension by Age and Sex, United States, NHANES 1999-2002
Age-Group, Years
US Population 2002
Mean Systolic Blood Pressure (95% CI),
mm Hg
Men 25-34 2,537,000 128 (121-135) 35-44 2,681,000 135 (130-141) 45-54 2,116,000 138 (133-143) 55-64 1,116,000 142 (136-148) 65-74 693,000 139 (138-144) ≥75 436,000 150 (141-159)
Women
25-34 2,792,000 126 (121-130) 35-44 3,024,000 135 (130-141) 45-54 2,460,000 142 (136-147) 55-64 1,438,000 141 (136-146) 65-74 977,000 148 (142-153) ≥75 849,000 152 (145-159)
NHANES = National Health and Nutrition Examination Survey; CI = confi dence interval.
Table 2. Differences in Mean Systolic Blood Pressures by Age and Sex Between Blacks With Hypertension vs the Black Population and vs Non-Hispanic Whites With Hypertension
Group
Difference in Systolic Blood Pressure, mm Hg
Blacks With Hypertension vs Entire Black
Population
Blacks With Hypertension
vs Whites With Hypertension
Men Age-group, years
25-34 8 1 35-44 9 7 45-54 7 9 55-64 5 10 65-74 1 3 ≥75 6 9
Unweighted mean Δ 6.0 6.5
Women Age-group, years
25-34 12 14 35-44 13 13 45-54 12 10 55-64 3 4 65-74 1 4 ≥75 2 1
Unweighted mean Δ 6.5 8.2
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in SBP increased the number of deaths
from heart disease by 43% and that
from stroke by 49%. Use of the 95%
upper and lower CIs yielded roughly
8% to 15% variations in estimates for
heart disease deaths and 18% to 22%
variations in those for stroke deaths.
Last, substitution of age- and sex-spe-
cifi c relative risk values from observa-
tional studies for those from treatment
studies yielded a 9% higher estimate
of deaths from heart disease and a 21%
lower estimate of deaths from stroke
relative to the base case, but very simi-
lar estimates of death from heart disease
and stroke combined (7,670 vs 7,720).
DISCUSSION Our fi ndings show that racial disparity
in SBP control contributes to nearly
8,000 excess deaths annually from
heart disease and stroke among blacks.
These fi ndings are fairly robust to
changes in key model assumptions. Pre-
vious analyses have shown that hyper-
tension is the single largest contributor,
of any medical condition, to racial disparity in adult
mortality.2 This excess mortality results from a com-
bination of a higher age-adjusted prevalence of hyper-
tension and poorer control of blood pressure among
those under treatment.3 Our analysis estimated the
contribution of just the latter factor to deaths among
blacks, but nonetheless, found a substantial impact on
the number of deaths in this racial group.
To our knowledge, this study represents the fi rst
effort to quantify the toll of racial disparities in blood
pressure control. Given the high prevalence of hyper-
tension in blacks, appreciable benefi ts of blood pres-
sure reduction, and signifi cant disparity in control, it is
not surprising that disparity in blood pressure control
results in appreciably more deaths than those estimated
from other health care disparities, including infl uenza
vaccination, mammography screening, use of β-block- ers after myocardial infarction, treatment of childhood
asthma, and diabetes.6,7
The causes of racial disparity in blood pressure
control are not known.12 There are several potential
explanations—differences in access to care, clini-
cian management, hypertension severity, and patient
adherence. Surprisingly, NHANES data show no
racial difference in treatment among all patients with
hypertension, suggesting that rates of diagnosis and
treatment among blacks in this sample are the same
Table 3. Black Mortality Rates by Age, Sex, and Blood Pressure
Group
Entire Black Populationa
Black Adults With
Hypertensionb
With Racial Parity in Blood
Pressure Controlb
Heart Disease Stroke
Heart Disease Stroke
Heart Disease Stroke
Men
Age-group, years 25-34 65 12 85 19 83 19
35-44 107 20 146 33 121 24
45-54 246 47 314 69 246 44
55-64 605 110 709 141 542 87
65-74 1,192 262 1,225 273 1,130 236
≥75 3,556 864 4,047 1,017 3,177 659
Age adjusted 419 90 733 167 603 140
Women
Age-group, years
25-34 24 7 39 11 7 6
35-44 58 17 98 28 89 15
45-54 125 36 186 54 142 33
55-64 312 70 334 75 277 54
65-74 734 181 758 187 680 154
≥75 3,438 975 3,527 1,000 3,433 953
Age adjusted 400 109 589 159 538 136
Note: mortality rates are expressed as number of deaths per 100,000.
a Data from Kochanek and Smith.8 b Derived estimates. See Methods for calculation details.
Table 4. Annual Deaths From Heart Disease and Stroke Avoided or Postponed Among Blacks Through Parity in Blood Pressure Control Between Black and White Adults With Hypertension, by Age and Sex
Group
Annual No. of Deathsa
Heart Disease Stroke
Men Age-group, years
25-34 10 0 35-44 120 50 45-54 480 170 55-64 940 300 65-74 420 160 ≥75 1,450 600
Overall 3,420 1,280
Women
Age-group, years
25-34 50 20 35-44 230 110 45-54 420 200 55-64 560 210 65-74 440 190 ≥75 360 180
Overall 2,060 910 Men and women 5,480 2,190
a Derived estimates. See Methods for calculation details.
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as among whites.3 Although there is considerable
evidence for racial disparity in management of car-
diovascular disease,13 there is little evidence of racial
disparity in treatment of hypertension. Specifi cally,
among those with hypertension, there is no signifi cant
difference in rates of drug treatment of hypertension
by race.12 In addition, some data suggest no difference
in clinician adherence to national hypertension treat-
ment guidelines or intensifi cation of antihypertensive
treatment by race.14
It is possible that blacks have more severe hyper-
tension or respond less favorably to antihypertensive
drugs. There is no clear evidence, however, for racial
differences in severity, and meta-analyses of treatment
trials show a similar response to antihypertensive medi-
cation by race, with whites having a slightly greater
response to β-blockers and blacks having a slightly greater response to diuretics.15
There is evidence for racial disparity in patient
adherence to antihypertensive medication, including
studies conducted within the Veterans Administra-
tion Health System, where fewer differences in access
appear to exist.16-18 Differences in adherence by race
may be due to affordability of medicines, personal
beliefs, anticipated adverse effects, and health literacy
that disproportionately affect blacks.18-20
Although multiple causes may contribute to racial
disparity in blood pressure control, this disparity is
not inevitable. Disparity in hypertension control is
signifi cantly smaller in the Veterans Administration
Health System, where access barriers are fewer.21 Little
or no disparity in blood pressure control was noted in
the treatment arms of 2 large community-based hyper-
tension treatment trials, the Hypertension Detection
and Follow-up Program and the Multiple Risk Factor
Intervention Trial.22,23 It is thus probable that elimina-
tion of racial disparity in SBP is an attainable goal, pro-
vided suffi cient resources are available to discover and
address adherence barriers.
The strengths of this study include use of a nation-
ally representative sample to estimate blood pressures
among persons with hypertension; use of race-, sex-,
and age-specifi c national mortality rates for heart
disease and stroke; and estimates of relative risk associ-
ated with SBP derived from meta-analyses.
The limitations of our study merit comment. The
sample of hypertensive blacks, although derived from
a nationally representative sample, was relatively small.
CIs surrounding estimates of blood pressure for spe-
cifi c groups were therefore relatively wide. Because
the number of deaths rises exponentially with age,
even small variation in estimates of racial disparity
in blood pressure among the elderly blacks can yield
appreciable changes in estimates. This phenomenon
is best illustrated by the results for women. Despite
a higher black-white disparity in SBP, our fi ndings
showed that elimination of this disparity would reduce
deaths more among black men than among black
women because the disparity for women is skewed
toward younger ages. It is for this reason that use
of a constant SBP yielded much higher estimates
for women than men. In addition, because of small
subgroup sizes, we used an upper age category of 75
years or older. Mean life expectancy at birth in 2004
was 69.5 years for black men and 75.3 years for black
women.1 Use of this cutoff underestimates the impact
of these disparities on deaths among elderly black
women. For these reasons, fi ndings that racial dispar-
ity in SBP disproportionately affects male mortality
should be viewed with caution pending more precise
estimates of racial disparity in blood pressure control
among men and women of advanced age.
These caveats notwithstanding, our fi ndings sug-
gest that racial disparity in hypertension control con-
tributes appreciably to deaths among blacks from heart
disease and stroke. Our analyses highlight the need
to more fully understand the causes of these dispari-
ties and develop viable strategies to eliminate them,
particularly clinician attention to adherence barriers
among patients.
To read or post commentaries in response to this article, see it online at http://www.annfammed.org/cgi/content/full/6/6/497.
Key words: Race/ethnicity; blacks; mortality; heart disease; stroke; hypertension; blood pressure; control
Submitted October 28, 2007; submitted, revised, January 29, 2008; accepted March 3, 2008.
Funding support: Funding was provided by the Robert Wood Johnson Foundation and by a grant from the National Heart, Lung, and Blood Institute (R01 HL081066-01A2).
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