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From the Center for Health Promotion, (L.R.Y., T.F.M., J.V.R., R.M.Y.,
D.M.B.); the Division of Cardiology (R.S.B., L.C.B.); and the School of
Nursing (M.N.H.), The Johns Hopkins Medical Institutions, Baltimore, Md.
First-degree relatives of persons with premature CHD have been shown to
have a 2-fold to 12-fold increased risk of
CHD.2 3 4 5 6 Among primary relatives, siblings of
persons with clinically documented CHD bear the highest risk for future
CHD events,7 and they have also been shown to
have a high prevalence of multiple CHD risk
factors.8
High BP is well known to be a major modifiable risk factor for
CHD.9 Accordingly, the NHBPEP was established in
1972, and the first JNC report was released in 1977, with the most
recent update in 1997 (JNC-VI).1 10 11 National
trends have shown increasing awareness, treatment, and control of
hypertension.12 13 14 We have observed low levels
of perceived risk for cardiovascular disease in prior
studies of siblings of patients with premature
CHD,15 suggesting also that the levels of
awareness, treatment, and control of hypertension among siblings might
also be low. Furthermore, our prior studies have shown a high
prevalence of other known risk factors in siblings (D.M.B., R.M.Y.,
T.F.M., R.S.B., L.C.B., unpublished data, 1997). Given siblings' high
relative risk for premature CHD, we designed this study to examine (1)
the prevalence of hypertension according to the JNC-V guidelines, (2)
awareness, treatment, and control, and (3) the prevalence of additional
risk factors in all apparently healthy siblings of persons with
premature CHD.
Measurement
After participants had fasted for at least 12 hours overnight,
venipuncture was performed to obtain blood samples for
direct measurements of serum levels of total cholesterol,
HDL cholesterol, triglycerides, and glucose.
LDL cholesterol levels were calculated using the Friedewald
equation for those subjects with triglyceride levels lower
than 4.52 mmol/L (400 mg/dL).16 All lipid
measurements were performed in the Johns Hopkins Chemistry Laboratory
using Lipid Research Program methods.17 Quality
control was maintained by the Johns Hopkins Lipid Research Clinic
Laboratory according to Centers for Disease Control standards. The
coefficient of variation for cholesterol measurement is
<3% in this laboratory.
Anthropometric measurements were obtained with subjects in light
clothing, without shoes. Height was measured on a stadiometer, and
weight on a balance scale. BMI was calculated as weight (kg) divided by
height (m) squared.
Demographic information, self-reported medical history, medication use,
and smoking information were obtained from a standardized interview.
Self-reported smoking status was confirmed by exhaled carbon monoxide
levels (>8 ppm indicated a current smoker). Dietary information was
obtained in a subsample (n=534) using a modified Block Food Frequency
Questionnaire18 characterizing intake in the
previous month. Physical activity was assessed in a subsample (n=428)
using questions from the Health Insurance Plan of New York
questionnaire.19
BP was measured using a standard mercury sphygmomanometer, following
the American Heart Association20 and JNC
guidelines.11 21 22 23 The mean of three resting BP
readings, taken early morning, midday, and late afternoon during the
screening day was used to characterize BP. Hypertension was defined as
the subject having a mean SBP of
JNC-V Report
Siblings were classified according to JNC-V guidelines: optimal (BP
<120/80 mm Hg); normal (SBP 120 to 129 mm Hg, DBP 80 to
84 mm Hg); high normal (SBP 130 to 139 mm Hg, DBP 85 to
89 mm Hg); stage 1 or mild hypertension (SBP 140 to 159
mm Hg, DBP 90 to 99 mm Hg); stage 2 or moderate hypertension
(SBP 160 to 179 mm Hg, DBP 100 to 109 mm Hg); stage 3 or
severe hypertension (SBP 180 to 209 mm Hg, DBP 110 to 119
mm Hg); and stage 4 or very severe hypertension (SBP
NHANES III
Analyses
Hypertension
Males tended to have a higher prevalence of hypertension (crude
OR=1.27, 95% CI=0.97 to 1.7). African Americans were significantly
more likely than whites to be hypertensive (crude OR=1.67, 95% CI=1.19
to 2.35). The prevalence of hypertension increased as decade of age
increased (
A high prevalence of other CHD risk factors was observed among those
found to be hypertensive (Table 1
Awareness, Treatment, and Control
Overall, hypertensive women were slightly but not significantly more
likely than men to be aware of their hypertension (OR=1.47, 95%
CI=0.97 to 2.22), significantly more likely to be under treatment
(OR=2.82, 95% CI=1.85 to 4.28), and significantly more likely to be
under control for their hypertension (OR=2.17, 95% CI=1.25 to 3.85).
When the comparison of control was limited to those currently under
treatment, there were no differences between women and men.
African Americans were slightly but not significantly more likely to be
aware of their hypertension (OR=1.58, 95% CI=0.96 to 2.61) and tended
to be more likely to be receiving treatment in comparison with white
siblings (OR=1.32, 95% CI=0.82 to 2.12), although this finding is not
statistically significant.
Older persons (age 45 to 59 years) were somewhat more likely to be
aware of their hypertension. There was a trend by decade (30 through
39, 40 through 49, or 50 through 59 years of age) for older persons
also to be significantly more likely to be under treatment for their
hypertension (
There were no differences in rates of awareness, treatment, or control
by high school completion compared with less than a high school
education.
NHANES Comparison
Siblings experienced higher rates of hypertension than the NHANES III
population, across race, gender, and age levels (Table 2
Interventions
Among those siblings who were being treated for hypertension with
pharmacological agents (n=170), monotherapy was far more common (72%)
than combination therapy (28%). Diuretics were the most common
agents used, both as monotherapy (35%) and as part of combination
therapy (84%). There were no significant differences between
monotherapy and combination therapy in control of hypertension.
The JNC-VI guidelines clearly extend the earlier mandate for
prevention, early detection, and treatment of high BP. These new
guidelines emphasize the importance of primary prevention and reinforce
patient education and methods to improve patient compliance. They also
provide physicians with very clear pathways for both lifestyle
modification and pharmacological care. A family history of premature
cardiovascular disease is again noted as a major factor
in risk stratification and medical management. This study produces
strong evidence that apparently healthy siblings of persons with
premature coronary disease have a high prevalence of elevated
BP levels and are not following lifestyle recommendations or receiving
appropriate care for hypertension. Aggressive dissemination of these
new guidelines will be necessary to create an impact on these high-risk
families, as it appears that the prior guidelines have not been
adequately applied to these individuals. As a recent JAMA
article and editorial suggest, the JNC-VI guidelines may need to be
disseminated on a wider scale to have any impact on physician
practices.28 29
Comparisons with national cross-sectional data still show the
prevalence of awareness, treatment, and control of hypertension to be
significantly lower among siblings than among the general population.
Again, this indicates a need for greater awareness among providers
about the uniquely high-risk status of persons in families with
premature coronary disease.
From a familial-clustering and heritability perspective, it would have
been interesting to observe BP differences between these siblings and a
control group without a family history. However, the research question
in this study was quite different. The purpose was to examine the
deviation of apparently healthy siblings at high risk for premature CHD
from national reference norms for BP.
A limitation of this study may be the exclusion of insulin-dependent
diabetics, which may have resulted in an underestimate of the
prevalence of hypertension and other CHD risk factors. Siblings were
accrued over a period of 13 years. Depending on the time of their
baseline examinations, they could have fallen into 1 of 4 JNC treatment
recommendation sets. However, statistical tests showed no significant
differences in prevalence of hypertension (P=0.611) or
treatment of hypertension (P=0.397) when comparing siblings
by which JNC report would have been in practice at the time of
screening. Finally, the classification recommendations for BP screening
were intended to be applied to measures of BP over multiple days. The
screening process for siblings took place all in 1 day, so it was not
possible to do this. To determine the extent to which multiple
measurements on a single day may have produced an overestimation of
high BP in comparison to the NHANES referents in which multiple
measures were accrued on different days, data from a 10% subsample of
siblings who returned for a substudy within 3 months of their initial
screening showed a high correlation of BPs (SBP r=0.66; DBP
r=0.70) and strong agreement for hypertension classification
(
Conclusion
Presented in part at the Scientific Sessions of the American College of Cardiology, Anaheim, Calif, March 16, 1997, and published in abstract form (J Am Coll Cardiol. 1997;29[suppl A]:48A49A).
Received December 17, 1997;
first decision January 9, 1998;
accepted February 20, 1998.
2.
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5.
Snowden CB, McNamara PM, Garrison RJ, Feinleib M,
Kannel WB, Epstein FH. Predicting coronary heart disease in
siblings: a multivariate assessment: the Framingham
Heart Study. Am J Epidemiol. 1982;115:217222.
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Hunt SC, Williams RR, Barlow GK. A comparison of
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Nora JJ, Lortscher RH, Spangler RD, Nora AH,
Kimberling WJ. Genetic epidemiologic study of early-onset
ischemic heart disease. Circulation. 1980;61:503508.
8.
Becker DM, Becker LC, Pearson TA, Fintel DJ, Levine
DM, Kwiterovich PO. Risk factors in siblings of people with premature
coronary heart disease. J Am Coll Cardiol. 1988;12:12731280.[Abstract]
9.
Whelton PK. Epidemiology of
hypertension. Lancet. 1994;344:101106.[Medline]
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10.
Joint National Committee on Detection, Evaluation, and
Treatment of High Blood Pressure. Report of the Joint National
Committee on Detection, Evaluation, and Treatment of High Blood
Pressure. JAMA. 1977;237:255261.
11.
Joint National Committee on Detection, Evaluation, and
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National Committee on Detection, Evaluation, and Treatment of High
Blood Pressure (JNC-V). Arch Intern Med. 1993;153:154183.
12.
Nieto FJ, Alonso J, Chambless LE, Zhong M, Ceraso M,
Romm FJ, Cooper L, Folsom AR, Szklo M. Population awareness and control
of hypertension and hypercholesterolemia.
Arch Intern Med. 1995;155:677684.
13.
Burt VL, Cutler JA, Higgins M, Horan MJ, LaBarthe DR,
Whelton P, Brown C, Roccella EJ. Trends in the prevalence, awareness,
treatment, and control of hypertension in the adult US population: data
from the Health Examination Surveys, 1960 to 1991.
Hypertension. 1995;26:6069.
14.
Sytkowski PA, D'Agostino RB, Belanger AJ, Kannel WB.
Secular trends in long-term sustained hypertension, long-term
treatment, and cardiovascular mortality: the Framingham
Heart Study 1950 to 1990. Circulation. 1996;93:697703.
15.
Becker DM, Levine DM. Risk perception, knowledge, and
lifestyles in siblings of people with premature coronary
disease. Am J Prev Med. 1987;3:4550.[Medline]
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16.
Friedewald WT, Levy RI, Fredrickson DS. Estimation of
the concentration of low-density lipoprotein cholesterol in
plasma, without use of the preparative ultracentrifuge.
Clin Chem. 1972;18:499502.[Abstract]
17.
Myers GL, Cooper GR, Winn CL, Smith SJ. The Centers for
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Standardization Program: an approach to accurate and precise lipid
measurements. Clin Lab Med. 1989;9:105135.[Medline]
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18.
Block G, Rosenberger WF, Patterson BH. Calories, fat,
and cholesterol: intake patterns in the US population by
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19.
Shapiro S, Weinblatt E, Frank CW, Sager RV. The HIP
study of incidence and prognosis of coronary heart disease:
preliminary findings on incidence of myocardial infarction and angina.
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20.
Frohlich ED, Grim C, LaBarthe DR, Maxwell MH, Perloff
D, Weidman WH. Recommendations for human blood pressure determination
by sphygmomanometers: report of a special task force appointed by the
Steering Committee, American Heart Association.
Hypertension. 1988;11:209A222A.
21.
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Committee on Detection, Evaluation, and Treatment of High Blood
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© 1998 American Heart Association, Inc.
Scientific Contributions
Hypertension Among Siblings of Persons With Premature Coronary Heart Disease
![]()
Abstract
Top
Abstract
Introduction
Methods
Results
Discussion
References
AbstractTo determine the extent to
which the Fifth Joint National Committee on Detection, Evaluation, and
Treatment of High Blood Pressure (JNC-V) guidelines were implemented in
high-risk families with premature coronary heart disease, we
examined the prevalence of hypertension and associated coronary
risk factors in asymptomatic siblings of persons with
documented premature coronary disease (<60 years of age). A
total of 859 apparently healthy siblings (51% male, 19% African
American) were screened for coronary risk factors. Siblings
were classified as normotensive or hypertensive (BP
140/90 and/or
current antihypertensive pharmacotherapy). The prevalence of
hypertension, awareness, treatment, and control among siblings was
compared with published national estimates from the third National
Health and Nutrition Examination Survey. The prevalence of hypertension
in siblings was 44%. Among all hypertensives, only 60% were aware of
being hypertensive, 45% were being treated, and 16% were under
control. A high prevalence of other coronary risk factors was
found among hypertensive siblings: 72% were
hypercholesterolemic; 61% were obese; 29% were
current smokers; 82% were consuming >30% of calories from fat; and
only 14% were participating in vigorous physical activity three or
more times per week. Comparisons with the national reference population
revealed siblings to have a significantly higher prevalence of
hypertension, along with significantly lower levels of awareness,
treatment, and control. These findings demonstrate the intersection of
multiple risk factors among hypertensive siblings and emphasize the
need for more aggressive screening and treatment in this easily
identifiable high-risk population.
Key Words: blood pressure prevalence hypertension, detection and control risk factors family
![]()
Introduction
Top
Abstract
Introduction
Methods
Results
Discussion
References
The newly released
Sixth Report of the Joint National Committee on Prevention, Detection,
Evaluation, and Treatment of High Blood Pressure again emphasizes the
importance of increased BP levels as a risk factor for
cardiovascular disease.1 Some
populations have shown clear benefit of the JNC guidelines and the
efforts of the NHBPEP for detection and treatment of hypertension. It
is not clear to what extent this has been true in families at very high
risk for CHD, particularly at a young age.
![]()
Methods
Top
Abstract
Introduction
Methods
Results
Discussion
References
Sample
Persons with premature CHD (<60 years of age) were identified
during hospitalization for a documented CHD event (acute myocardial
infarction, coronary artery bypass surgery, coronary
angioplasty, or angina with angiographic documentation of at least 1
coronary artery with
50% stenosis) in 1 of 7
Baltimore area hospitals. A sequential purposive sample was accrued by
recruitment on specific days in all institutions, so that all patients
available at the target recruitment day and week were recruited. Index
cases were interviewed in the hospital and asked for access to their
siblings. Siblings who were reported to be <60 years of age and free
of CHD were mailed an explanation of the study and asked to return a
postcard if they declined to participate. Unless the refusal card was
received, siblings were telephoned to determine eligibility, defined as
aged <60 years, no clinical CHD, not receiving
glucocorticosteroid or insulin therapy, and no
life-threatening illness (eg, cancer or AIDS). Overall enrollment rates
were approximately 70%.
Written informed consent was received from all siblings, and the
approval of the Johns Hopkins Medical Institutions Joint Committee on
Clinical Investigation was received for all procedures. Eligible
siblings underwent a physical examination, phlebotomy, anthropometric
and BP measurements, and a resting ECG.
140 mm Hg, a mean DBP of
90 mm Hg, and/or currently taking an antihypertensive
medication. This is the standard for defining hypertension for the
purpose of examining awareness, treatment, and
control.11
JNC-V, published in 1993, included updated recommendations for
classification and management of hypertension.11
The definition of hypertension (
140/90 mm Hg) has not changed
since the first JNC report in 1977; however, JNC-V described
"stages" of hypertension for the first time. Treatment guidelines
were refined and encouraged a combination of aggressive lifestyle
modifications before pharmacological interventions. JNC-VI continued
this stage classification and intervention combination, while placing
more emphasis on prevention and the discrimination of risk groups.
210
mm Hg, DBP
120 mm Hg). When systolic and
diastolic pressures led to different categorizations,
individuals were classified into the higher stage. The only difference
between JNC-V and JNC-VI in terms of classification of stages is that
JNC-VI combines stages 3 and 4 because of the rarity of stage 4
hypertension.
NHANES III was designed to estimate the prevalence of certain
diseases and conditions in the civilian, noninstitutionalized
population of the United States. This survey collected data through
interviews and direct examinations and was conducted during 2 phases.
The first phase, which took place from 1988 to 1991, was used as a
reference population for comparison of prevalence, awareness,
treatment, and control among hypertensives.24
NHANES III assessment and analysis methods have been described
in detail elsewhere.25
All analyses were performed using the SAS
software.26 Comparisons were made by contingency
table arrays and were analyzed using the
2 statistic for categorical variables and
Student's t test for continuous data. Multiple logistic
regression was used to obtain adjusted ORs; 95% CIs were then
calculated.
![]()
Results
Top
Abstract
Introduction
Methods
Results
Discussion
References
Sample Characteristics
A total of 859 siblings from 490 families (mean, 1.8±1 siblings
per family) were included in this analysis. Eligible siblings
were enrolled into the Johns Hopkins Sibling Study between 1983 and
1996. The sample was 51% female, 19% African American, with a mean
age of 45.8±7 years (range, 30 to 59 years). The average educational
level completed was 12.7±3 years, with 78% of the siblings having
completed high school. The overall prevalence of CHD risk factors was
high, with mean levels of total and LDL cholesterol and
triglycerides exceeding national averages and mean levels
of HDL cholesterol falling below national
averages.27
Using the JNC-V definitions, 37% of all siblings (n=479 of 859)
were classified as currently hypertensive: 27% were stage 1, 9% were
stage 2, and 1% were stage 3 or 4. Only 15% of all siblings had
optimal BP, while 22% were normal and 26% were classified as high
normal. Including those siblings who were currently taking
antihypertensive medications but were under control, 44% of the sample
(n=380 of 859) was classified as hypertensive. The overall mean SBP was
133.0±16 mm Hg, and the overall mean DBP was 84.6±10
mm Hg for the total group of 859 siblings.
2 for trend=62.9,
P=0.001).
). When
adjusting for age, hypertensive siblings were significantly more likely
than normotensive siblings (BP <140/90 mm Hg) to be obese (for
women, BMI
27.3; for men, BMI
27.8) and to have elevated total
cholesterol, triglyceride, and LDL
cholesterol levels. There was no difference in the
prevalence of high fat diets (
30% of calories from fat) or vigorous
physical activity (
3 times per week) between hypertensive and
normotensive siblings. Hypertensive siblings were significantly less
likely to be current smokers and significantly more likely to be former
smokers than normotensive siblings. When the risk factors
presented in Table 1
were summed for each sibling, those with
hypertension were found to have a significantly higher mean number of
risk factors (smoking, obesity, inactivity, high fat diet,
hyperlipidemias) than those with normal BP (3.4 versus
2.9, P=0.0001).
View this table:
[in a new window]
Table 1. Age-Adjusted Prevalence of CHD Risk Factors Among
Siblings (n=859)
Among all hypertensive siblings (n=380), 60% were aware, 45%
were currently receiving pharmacological treatment, and 16% were under
control. Differences by gender are shown in Figure 1
. Control in siblings currently
receiving antihypertensive therapy was 36% (n=61 of 170).

View larger version (25K):
[in a new window]
Figure 1. Awareness, treatment, and control among
hypertensive siblings (n=380) by gender. *Hypertension is defined as BP
140/90 mm Hg and/or current antihypertensive
pharmacotherapy.
2 for trend=6.85,
P=0.009). Of those being treated, by decade, older persons
were significantly more likely to be under control
(
2 for trend=4.59, P=0.032).
To determine the validity of using NHANES III data for reference
comparisons, the entire sibling sample was divided into 3 groups by
time of screening: 1983 through 1987, pre-NHANES III; 1988 through
1991, during NHANES III (phase I); and 1992 through 1996, post-NHANES
III (phase I). Mean SBP and DBP levels among all siblings from 1983
through 1987, 1988 through 1991, and 1992 through 1996 showed only very
small decrements over time (systolic 134.7±16, 134.4±12,
132.1±16 mm Hg; diastolic 86.0±10, 85.5±9,
83.9±10 mm Hg, respectively). There were also no significant
differences in the prevalence of hypertension or the categories of
hypertension among siblings by these time periods.
) and all stages of hypertension (Figure 2
). Awareness, treatment, and control of
hypertension levels were consistently lower among siblings than
in the NHANES III population (Figure 3
)
across race and gender levels (Table 3
).
When the analysis was stratified by age groups, the number of
siblings in each group became too small to analyze.
View this table:
[in a new window]
Table 2. Prevalence of Hypertension Among Siblings and NHANES
III Population by Age, Race, and Gender

View larger version (15K):
[in a new window]
Figure 2. Comparison of the distributions of BP levels
between all siblings (n=859) and the NHANES III (phase I) sample.

View larger version (14K):
[in a new window]
Figure 3. Comparison of awareness, treatment, and control of
hypertension between siblings and the NHANES III sample. Hypertension
is defined as BP
140/90 mm Hg and/or current antihypertensive
pharmacotherapy.
Percentage of all hypertensives (n=380).
Percentage of treated hypertensives (n=170).
View this table:
[in a new window]
Table 3. Prevalence of Awareness, Treatment, and Control of
Hypertension Among Hypertensive Siblings and NHANES III (Phase
I) Population
Few hypertensive siblings self-reported any lifestyle efforts to
treat high BP. Analysis of a subsample in whom diet and
physical activity were assessed showed that more than three quarters of
those with hypertension were overweight and did not participate in any
regular physical activity. Almost two thirds of those with hypertension
were consuming >2500 mg/d sodium in foods alone, and the mean sodium
consumption for hypertensive siblings was 2893±1007 mg/d. Eleven
percent of hypertensive siblings were consuming more than 10% of
calories as alcohol. These measures of lifestyle were virtually the
inverse of those reported by NHANES III participants, among whom more
than three quarters of hypertensive individuals reported the use of 1
or more nonpharmacological or lifestyle therapies, as opposed to only
one quarter of the hypertensive siblings in the present study.
![]()
Discussion
Top
Abstract
Introduction
Methods
Results
Discussion
References
This study shows that siblings of persons who have had a premature
CHD event are not adequately aware of, treated for, or controlled for
hypertension. One possible reason for this poor awareness, self-care,
and medical care is that siblings do not perceive themselves to be at
risk for CHD events.15 Anecdotally, siblings in
this study at the time of screening interviews quickly pointed out the
ways in which they were different from the sibling who had the CHD
event. Also, siblings often seemed interested in screening primarily to
reassure themselves that they were not at risk.
=0.69, 95% CI=0.54 to 0.85). It is unlikely that the single-day
measures produced sufficient bias to have influenced our
conclusions.
Siblings of persons with premature CHD are a high-risk population
with an increased prevalence of hypertension in combination with high
levels of other modifiable CHD risk factors and inadequate levels of
awareness, treatment, and control. Physician recommendations that
promote lifestyle changes have a high probability of potentially
lowering BP levels, as well as influencing concomitant risk factors, if
persons are compliant. Given the inadequate levels of control among
hypertensive siblings receiving therapy, pharmacological treatment may
need to be more closely monitored and aggressively adapted to achieve
optimal levels of BP. Siblings are an easily identifiable high-risk
group who remain in need of improved screening and effective treatment
strategies to lower rates of hypertension.
![]()
Selected Abbreviations and Acronyms
BMI
=
body mass index
BP
=
blood pressure
CHD
=
coronary heart disease
CI
=
confidence interval
DBP
=
diastolic blood pressure
JNC
=
Joint National Committee on Detection, Evaluation, and Treatment of
High Blood Pressure
NHANES
=
National Health and Nutrition Examination Survey
NHBPEP
=
National High Blood Pressure Education Program
OR
=
odds ratio
SBP
=
systolic blood pressure
![]()
Acknowledgments
This study was supported by grants NR0224103 from the National
Institute of Nursing Research, HL4976202 from the National Heart, Lung,
and Blood Institute, and RR-00035 and RR-00722 from the National
Institutes of Health for the General Clinical Research Center of the
Johns Hopkins University School of Medicine.
![]()
Footnotes
Reprint requests to Lisa R. Yanek, MPH, The Johns Hopkins Medical Institutions, Center for Health Promotion, 1830 E Monument St, Room 8021, Baltimore, MD 21205.
![]()
References
Top
Abstract
Introduction
Methods
Results
Discussion
References
1.
Joint National Committee on Prevention, Detection,
Evaluation, and Treatment of High Blood Pressure. The Sixth
Report of the Joint National Committee on Prevention, Detection,
Evaluation, and Treatment of High Blood Pressure. Rockville, Md:
National Institutes of Health, National Heart, Lung, and Blood
Institute, National High Blood Pressure Education Program; 1997. NIH
publication 984080.
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C K Chow, A C H Pell, A Walker, C O'Dowd, A F Dominiczak, and J P Pell Families of patients with premature coronary heart disease: an obvious but neglected target for primary prevention BMJ, September 8, 2007; 335(7618): 481 - 485. [Full Text] [PDF] |
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M. GLICK Screening for traditional risk factors for cardiovascular disease: A review for oral health care providers J Am Dent Assoc, March 1, 2002; 133(3): 291 - 300. [Abstract] [Full Text] [PDF] |
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A Baessler, C Hengstenberg, S Holmer, M Fischer, B Mayer, U Hubauer, G Klein, G Riegger, and H Schunkert Long-term effects of in-hospital cardiac rehabilitation on the cardiac risk profile. A case-control study in pairs of siblings with myocardial infarction Eur. Heart J., July 1, 2001; 22(13): 1111 - 1118. [Abstract] [PDF] |
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C Hengstenberg, S.R Holmer, B Mayer, S Engel, A Schneider, H Lowel, G.A.J Riegger, and H Schunkert Siblings of myocardial infarction patients are overlooked in primary prevention of cardiovascular disease Eur. Heart J., June 1, 2001; 22(11): 926 - 933. [Abstract] [PDF] |
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