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(Hypertension. 1998;31:97.)
© 1998 American Heart Association, Inc.
Scientific Contributions |
From the Division of Cardiology, Childrens Hospital Medical Center, Cincinnati, Ohio (S.R.D., F.M.B., J.A.M.); Maryland Medical Research Institute, Baltimore, Md (R.P.M., S.L.S., B.A.B.); the National Heart, Lung, and Blood Institute, Bethesda, Md (E.O., M.A.W.); Westat, Inc, Rockville, Md (G.B.S.); and the Department of Clinical Epidemiology and Preventive Medicine, University of Pittsburgh School of Medicine (Pa) (S.Y.S.K.).
Correspondence to Stephen R. Daniels, MD, PhD, Division of Cardiology, Childrens Hospital Medical Center, 3333 Burnet Ave, Cincinnati OH 45229. E-mail sdaniels{at}chmcc.org
| Abstract |
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Key Words: blood pressure race obesity adolescents
| Introduction |
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The NGHS is a prospective cohort study designed to evaluate the emergence of differences in obesity and cardiovascular risk factors during adolescence in black and white girls. The purpose of the present report is to describe the longitudinal changes in blood pressure in black and white girls from age 9 to age 14 years and to determine the presence and persistence of racial differences in blood pressure in the cohort over time. The determinants of longitudinal change in systolic and diastolic blood pressure over time and the presence of racial differences in the growth-related determinants of change were also evaluated.
| Methods |
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Subjects
NGHS enrolled 1213 black and 1166 white girls who were age 9 or
10 years at the onset of the study. Race was determined by
self-declaration by the girls and their parents or guardians. Girls
were eligible if they declared themselves black or white and there was
concordance between the racial declaration of the parents or guardians
and the child. Informed consent for participation was obtained from all
participants and their parents.
The subjects were examined once a year (within a 3-month window of the anniversary date). Data in this report include follow-up of the girls through age 14 years (through the fourth or fifth annual follow-up visit, depending on the age of the girl at entry). Age was defined as age at last birthday. Retention decreased slightly with time: at the fourth follow-up visit, 89.9% of black and 83.2% of white participants were seen at the annual visit for an overall participation rate of 86.6%.
Measurements
The methods for the NGHS have been described previously in
detail.12 Measurements of height, weight,
skinfold thickness, stage of sexual maturation, and blood pressure were
obtained by examiners who were trained and certified to follow a common
protocol. Examiners were retrained yearly, and consistent
methods of measurement were maintained throughout the study. Height was
measured using custom-made stadiometers with the girls wearing no
shoes. Weight was measured with calibrated Health-O-Meter electronic
scales with girls wearing provided T-shirts or gowns. Skinfold
measurements were obtained at the triceps, suprailiac, and subscapular
sites with Holtain calipers. All anthropometric measurements were taken
twice and repeated a third time if the first two measurements differed
by more than 0.5 cm (height), 0.3 kg (weight), or 1.0 mm (skin
folds). Degree of overweight and adiposity was assessed using BMI,
calculated as (weight in kilograms)/(height in meters squared), and sum
of the three skinfold thicknesses. The degree of adiposity was assessed
using the ratio of truncal (subscapular and suprailiac) to total sum of
skin folds. Blood pressure examiners received 16 hours of instruction,
and their techniques were evaluated before certification for blood
pressure measurement. Subjects were seated with feet resting on a flat
surface and the arm at heart level. The appropriate size cuff was
selected based on upper arm circumference. Blood pressure was measured
three times with measurements at least 60 seconds apart using a
standard mercury sphygmomanometer. The second and third measurements of
blood pressure were used to calculate the mean systolic and
diastolic K4 and K5 blood pressure.12
In the present analyses, measured values of
diastolic K5 blood pressure <20 mm Hg were treated
as missing data. The diastolic K5 blood pressure
measurement was substituted for the diastolic K4
measurement when K4 could not be distinguished from K5. Sexual
maturation staging was performed using criteria developed by Garn and
Falkner based on two indices, pubic hair and areolar development. These
stages were based on Tanner staging principles and modified for the
study of obesity.12 Specific areolar and pubic
hair staging plates were developed for evaluation of maturation. The
maturation stages were defined as follows: prepubertal girls were
premenarcheal and at stage 1 in both areolar and pubic hair
development; pubertal girls were premenarcheal, but at stage 2 or
greater in either areolar or pubic hair development; and postmenarcheal
girls had reported beginning their menses.
Statistical Methods
To examine racial differences with age, descriptive
statistics by race for anthropometry and blood pressure measures (means
and standard deviations) were calculated by age at last birthday.
Figures are presented showing mean blood pressure levels by age
and race; by age, race, and maturation stage; and by race and BMI at a
specific study visit (corresponding to ages 11 and 12 years) to display
associations of these variables with blood pressure. Means are not
presented for age-race-maturation stage or race-BMI
combinations for which fewer than 20 girls were observed. Because the
girls in the cohort were ages 9 or 10 at entry, and participants were
seen annually, data from different study visits were pooled in
calculating statistics by age, such as mean BMI at age 10.
Regression models were fitted to estimate the effects of age, race, height, BMI, and maturation stage on blood pressure. To account for the correlations among repeated observations from the same participant, the GEE method of Liang and Zeger13 was used to fit linear regression models. With this method, least-squares estimates of models were obtained, and residuals from the fitted model were used to adjust the standard errors of model coefficients to take account of within-individual correlations.
Increased sexual maturation is accompanied both by growth in height and in adiposity (estimated by BMI). Multivariable regression models were fitted incorporating terms for race, age, racexage interactions, and maturation stage. Terms for height and for BMI were added successively to these models, to see whether either or both accounted for the association of sexual maturation with increases in blood pressure. Tests were performed to determine whether the effects of height or BMI on blood pressure differed between blacks and whites. BMI was used as a measure of adiposity in these models for comparability with other studies. Analyses were also performed using sum of skin folds as a measure of adiposity rather than BMI; the results of those models were generally consistent with the analyses using BMI reported here.
Height and BMI were included in these models as continuous
variables. Age in years at last birthday was included in these
models by a set of indicator variables for ages 10 to 14 years,
with age 9 years as the reference level. Maturation stage was included
with indicator variables comparing pubertal and postmenarcheal
girls to prepubertal girls. Race was included using an indicator
variable with white girls used as the reference point. Tests of
interaction between race and age and between race and maturation stage
were performed using global tests for any difference between blacks and
whites in the effect of age or maturation, before testing for
black/white differences at particular ages or maturation stages.
Otherwise, these exploratory analyses did not attempt to adjust
values of probability to take into account the multiple tests required
to arrive at the final model. Interactions were also tested between
race and height and race and BMI. Values of P
.05 were
considered to indicate evidence of associations worth further
investigation.
| Results |
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The distribution of sexual maturation stage by age and race is shown in Table 3. Sexual maturation begins earlier for black than for white girls: a larger proportion of black girls than white girls have begun puberty at age 9 years, and by age 12 years, over 60% of the black girls have reached menarche compared with only 39% of the white girls. By age 14 years, over 90% of the girls from both race groups have reached menarche.
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In Fig 1A through 1C, mean values by race of longitudinal blood pressures (systolic, diastolic K4, diastolic K5) are displayed from age 9 to 14 years. Systolic and diastolic blood pressures increased with increasing age for both black and white girls, and black girls had higher average blood pressures than the white girls of corresponding age over the course of the study, with the smallest differences at age 13 years. This variation by age in the black/white difference in blood pressure is statistically significant for systolic blood pressure (P=.02) and diastolic K4 blood pressure (P=.03), but borderline significant for diastolic K5 blood pressure (P=.06).
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In Fig 2A through 2C, mean systolic and diastolic blood pressure levels are displayed by age, sexual maturation stage, and race. Within maturation stage groups, black girls generally have higher blood pressure than white girls at each age, although there is variation in the magnitude of the black/white difference over ages 9 to 14 years. Because increased sexual maturation is generally accompanied by increases in height and in BMI, longitudinal regression models were used to investigate whether the effects of sexual maturation on blood pressure were accounted for by these factors.
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Height was a highly significant predictor of blood pressure in all models, although adjustment for BMI and maturation stage reduced the predicted increase in blood pressure per centimeter increase in height from 0.28±0.02 mm Hg to 0.20±0.02 mm Hg for systolic and from 0.20±0.02 mm Hg to 0.15±0.02 for diastolic (K4 or K5). The effect of height on blood pressures did not differ by race (P>.3 for all comparisons).
After adjustment for age, race, and height, blood pressure remained related to sexual maturation stage. Mean blood pressure increased with increasing sexual maturation. After adjustment, it was estimated that the mean±SE blood pressure differences between pubertal and prepubertal girls were 1.2±0.3 mm Hg for systolic blood pressure (P<.001), 0.9±0.4 mm Hg for diastolic K4 blood pressure (P=.01), and 1.0±0.4 mm Hg for diastolic K5 blood pressure (P=.01). Similarly, after adjustment for age, race, and height, the estimated mean±SE blood pressure difference between postmenarcheal and pubertal girls was 1.6±0.3 mm Hg for systolic blood pressure (P<.001), 0.9±0.3 mm Hg for diastolic K4 blood pressure (P=.001), and 1.0±0.3 mm Hg for diastolic K5 blood pressure (P=.001). The relationship between maturation stage and diastolic (K4 or K5) blood pressure was similar in black and white girls, but there was some evidence (P=.05) for black/white differences in the effect of maturation stage on systolic blood pressure.
After the addition of BMI to the previous model, differences in blood pressure by maturation stage were no longer statistically significant, although trends remained for higher blood pressures with increasing sexual maturation. After age, race, height, BMI, and the agexrace and racexBMI interactions were added to the GEE regression model, the estimated mean±SE blood pressure differences between pubertal and prepubertal girls were as follows: systolic, 0.3±0.3 mm Hg (P=.29); diastolic K4, 0.6±0.4 mm Hg (P=.10); and diastolic K5, 0.7±0.4 mm Hg (P=.10). The estimated differences (±SE) in blood pressure between postmenarcheal and pubertal girls were as follows: systolic, 0.5±0.3 mm Hg (P=.08); diastolic K4, 0.5±0.3 mm Hg (P=.09); and diastolic K5, 0.6±0.3 mm Hg (P=.06). After adjustment for both height and BMI, estimated differences in blood pressure between prepubertal and pubertal, and pubertal and postmenarcheal girls were similar in blacks and in whites.
The effect of BMI on blood pressure differed between blacks and whites (P=.02, P=.004, and P=.02 for tests for interaction for systolic, diastolic K4, and diastolic K5 blood pressures, respectively). Using regression models, the average (±SE) increase in blood pressure per unit increase in BMI was larger in whites than in blacks: 0.65±0.04 mm Hg in whites (P<.001) and 0.52±0.04 in blacks (P<.001) for systolic blood pressure. For diastolic K4 and diastolic K5 blood pressure, the increase per unit increase in BMI in whites was approximately double that for blacks, 0.31±0.04 mm Hg in whites (P<.001) and 0.15±0.03 in blacks (P<.001) for diastolic K4 blood pressure; and, 0.31±0.05 mm Hg in whites (P<.001) and 0.16±0.04 in blacks (P<.001) for diastolic K5 blood pressure.
To illustrate, the relationship between BMI and blood pressure is depicted in Fig 3A through 3C for black and white girls at study visit 3 (ages 11 to 12 years). Whereas black girls tend to have higher blood pressure than white girls at lower levels of BMI, there is a steeper increase in blood pressure with increasing BMI in white girls than in black girls. This results in 11- and 12-year-old black and white girls having similar blood pressures at higher levels of BMI. The relationship between blood pressure and BMI in black and white girls at other ages was similar to that observed at ages 11 to 12 years. Because the effect of BMI on blood pressure differed in black and white girls, as demonstrated by GEE modeling, the magnitude of black/white differences in blood pressure depended on BMI. The magnitude of these racial differences at each level of BMI also depended on age (each P<.05).
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To evaluate the potential impact of regional differences in adiposity, the ratio of truncal to total sum of skin folds was included in the final model. This variable was not significantly associated with either systolic or diastolic blood pressure.
| Discussion |
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The timing of the onset of racial differences in blood pressure remains controversial. Cross-sectional studies in children and adolescents have yielded conflicting results. It is well known that cross-sectional studies may not provide a valid assessment of longitudinal changes.17 Manatunga et al18 conducted a longitudinal study of 345 white children and 164 black children with mean age of 9 years at baseline. In their study, blood pressure was measured every 6 months for 2 to 5.5 years. For girls the mean systolic and diastolic blood pressures were higher by 2 mm Hg and 1.5 mm Hg, respectively, in blacks compared with whites. After accounting for age, weight, height, and BMI, the racial difference in systolic blood pressure remained significant, but there was no significant difference in diastolic blood pressure between black and white girls. The rate of increase in systolic and diastolic blood pressure with age was significantly greater for black girls compared with white girls.
The results of the present study are consistent with those of Manatunga et al.18 At enrollment, there were already differences between the black and white girls, with the black girls having higher blood pressure. Systolic and diastolic blood pressure progressively increased with increasing age for both black and white girls, and black girls consistently had higher blood pressure than white girls. However, Manatunga et al did not evaluate the role of sexual maturation on blood pressure change. Kozinetz19 20 has suggested from cross-sectional analyses using self-assessment of maturation that there is an association between stage of sexual maturation and blood pressure in girls, and that observed racial differences in blood pressure could be explained by racial differences in the level of pubertal development. However, in the present study in which maturation was assessed according to a standard protocol by trained observers, black/white differences in blood pressure are seen at all stages of sexual maturation. This result is consistent with the concept that additional factors other than sexual maturation are also important in the racial difference of blood pressure in adolescent girls.
Blood pressure increases with increasing height and BMI in children and adolescents.21 22 23 Therefore, it is important to determine the extent to which height and BMI influence the observed longitudinal racial differences in blood pressure. Height was a significant explanatory variable in the regression models for systolic as well as diastolic K4 and K5 blood pressures. There was no interaction between race and height, suggesting that the effect of linear growth on blood pressure is similar for white and black girls. Although black girls were initially taller on average, by age 14, average height was greater in white than in black girls.
BMI was also a significant independent variable in the regression models for systolic and diastolic blood pressures. This finding is consistent with previous cross-sectional epidemiologic studies22 23 and with studies demonstrating that weight loss lowers blood pressure in obese adolescents.24 When height and BMI are both included in the regression model, the effect of sexual maturation on blood pressure is greatly attenuated. This finding supports the hypothesis that the increases in height and BMI accompanying sexual maturation are major contributors to changes in systolic and diastolic blood pressure seen as girls go through the sexual maturation process.
In the present study, there was a significant interaction between the effects of race and BMI on blood pressure. BMI had a smaller impact on blood pressure in black than in white girls. However, average BMI increased at a greater rate with age in black than white girls, which may have contributed to the black/white differences in blood pressure seen in Fig 1. It is of interest that the distribution of adiposity was not a significant correlate of blood pressure in this study.
There has been ongoing debate about the presence of racial differences in the relationship between BMI and blood pressure in adults. Some studies of adult populations have suggested that the association between BMI and blood pressure is weaker in blacks than whites,9 10 11 whereas others have found no racial differences in the relationship.25 26 27 28 In the present study, the racial difference in the BMIblood pressure relationship results in similar blood pressures for black and white girls at higher levels of BMI, whereas black girls seem to have higher blood pressures than whites at lower levels of BMI. These differences are not accounted for by black/white differences in sexual maturation stage. The etiology of the racial difference in blood pressure at lower BMI remains unexplained. This difference could be due to factors not included in the present analysis, such as dietary intake of sodium and potassium, sensitivity to sodium intake, or physical activity.29 During ages 9 to 14 years, BMI increased with age at a higher average rate in black girls than in white girls. This greater rate of increase in BMI in black girls helps account for the maintenance of racial differences in blood pressures during ages 9 to 14 years, despite the finding of a lower increase in blood pressure per unit increase in BMI in black girls compared with white girls. The mechanism for a racial difference in the relationship between BMI and blood pressure remains unknown. Future research should focus on a better understanding of this relationship.
NGHS demonstrates significant racial differences in blood pressure in girls 9 to 14 years of age, the years of prepuberty and early puberty to late puberty. If the higher blood pressures observed in black girls compared with whites continue during late adolescence and young adulthood, and if BMI increases to a greater extent in young black women, then large differences in blood pressure can be expected to be seen between black and white women. Understanding the determinants of this racial difference in blood pressure could provide the rationale for future interventions to reduce the excess cardiovascular morbidity and mortality seen in black women.
| Selected Abbreviations and Acronyms |
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| Acknowledgments |
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Received February 24, 1997; first decision May 5, 1997; accepted August 13, 1997.
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