|
|
||||||||
ORIGINAL RESEARCH COMMUNICATION |
1 From the Divisions of Nutrition and Physical Activity (DSF, ZM, LMG-S, and WHD) and Diabetes Translation (HSK), Centers for Disease Control and Prevention, Atlanta, GA, and the Tulane Center for Cardiovascular Health, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA (SRS and GSB)
2 The findings and conclusions in this report are those of the authors and not necessarily those of the CDC. 3 Supported by grant no. AG-16592 from the National Institutes of Aging. 4 Address reprint requests to DS Freedman, CDC K-26, 4770 Buford Highway, Atlanta GA 30341. E-mail: dfreedman{at}cdc.gov.
| ABSTRACT |
|---|
|
|
|---|
Objectives: We examined the relation of the BMI-for-age z score and waist-to-height ratio to risk factors (lipids, fasting insulin, and blood pressures). We also compared the abilities of these 2 indexes to identify children with adverse risk factors.
Design: Children aged 517 y (n = 2498) in the Bogalusa Heart Study were evaluated.
Results: As assessed by the ability of the 2 indexes to 1) account for the variability in each risk factor and 2) correctly identify children with adverse values, the predictive abilities of the BMI-for-age z score and waist-to-height ratio were similar. Waist-to-height ratio was slightly better (0.010.02 higher R2 values, P < 0.05) in predicting concentrations of total-to-HDL cholesterol ratio and LDL cholesterol, but BMI was slightly better in identifying children with high systolic blood pressure (0.03 higher R2, P < 0.05) in predicting measures of fasting insulin and systolic and diastolic blood pressures. On the basis of an overall index of the 6 risk factors, no difference was observed in the predictive abilities of BMI-for-age and waist-to-height ratio, with areas under the curves of 0.85 and 0.86 (P = 0.30) and multiple R2 values of 0.320 and 0.318 (P = 0.79). This similarity likely results from the high intercorrelation (R2 = 0.78) between the 2 indexes.
Conclusions: BMI-for-age and waist-to-height ratio do not differ in their abilities to identify children with adverse risk factors. Although waist-to-height ratio may be preferred because of its simplicity, additional longitudinal data are needed to examine its relation to disease.
Key Words: BMI body mass index waist height waist-to- height ratio children lipids blood pressure insulin
| INTRODUCTION |
|---|
|
|
|---|
The waist-to-height ratio was first used in the Framingham Study (17), and several studies of children (13-15) and adults (18, 19) have concluded that this ratio is more strongly associated with CVD risk factors than is the body mass index (BMI; in kg/m2). In addition, waist-to-height ratio may be simpler to use. For example, because waist-to-height ratio is only weakly associated with age, measures among children do not have to be expressed relative to their sex and age peers [by using z scores (20)] as do measures of BMI. In addition, the same cutoff (eg, 0.5) could possibly be used to identify adverse measures of waist-to-height ratio among both children and adults (21, 22), which would simplify the expression of obesity-related disease risk. However, relatively few studies have examined the relation of waist-to-height ratio to CVD risk factors, and it is important to examine these associations in other data.
The current study compares the relation of BMI and waist-to-height ratio to measures of lipids, fasting insulin, and blood pressure among 517-y-olds (n = 2498) in the Bogalusa Heart Study. In addition, we examine the abilities of these 2 indexes to correctly identify children with adverse risk factors.
| SUBJECTS AND METHODS |
|---|
|
|
|---|
Of the 3135 children and adolescents (aged 517 y) examined, we excluded 9 girls who reported being pregnant, 7 children who were not white or black, 30 children who reported taking insulin (or were unsure), 13 children for whom we did not have a systolic (SBP) or diastolic (DBP) blood pressure measurement, and 14 children for whom information on measurements of waist, weight, or height was missing; these categories were not mutually exclusive. Of the remaining 3066 children, cholesterol (total, LDL, and HDL) and triacylglycerol determinations were available for 2961. Nonfasting children were excluded from the analyses of triacylglycerol and fasting insulin concentrations, and another 130 children did not have an insulin determination. After these exclusions, sample sizes for the various risk factors are 3066 (for SBP and DBP), 2961 (for LDL and HDL cholesterol), 2624 (for triacylglycerol), and 2494 (for insulin).
Because obesity is associated positively with LDL cholesterol and negatively with HDL cholesterol, we did not examine associations with total cholesterol. However, the ratio of total cholesterol to HDL cholesterol (total:HDL cholesterol) is included in the analyses.
General examinations
Height was measured to the nearest 0.1 cm with the use of an Iowa Height Board, and weight was measured to the nearest 0.1 kg with the use of a balance beam metric scale; BMI was calculated as a measure of relative weight. No adjustments were made for the weight of the gown, underpants, or socks that were worn during the examination.
BMI z scores were calculated from the 2000 Centers for Disease Control and Prevention (CDC) Growth Charts (20, 24) to account for the differences in BMIs by sex and age. These growth charts express the BMIs of children in the current study relative to their sex and age peers in the United States between 1963 and 1980; the calculated z scores are termed "BMI-for-age" in the current analyses. (BMIs among 5-y-olds in the CDC Growth Charts also include data from 19881994.) Overweight is defined as a BMI-for-age z score
1.645 (corresponding to the 95th percentile of normally distributed data) of these growth charts (25, 26). BMI-for-age z scores were used in all analyses in the current study. BMI-for-age percentiles are used only to classify children into 4 categories in one table that cross-classifies BMI-for-age and waist-to-height ratio.
The waist circumference was measured midway between the rib cage and the superior border of the iliac crest while the child was standing. Three measurements were obtained with a nonstretchable tape, and the mean value was used in the calculation of the waist-to-height ratio. In analyses that compared the abilities of BMI and waist-to-height ratio to correctly identify children with adverse risk factors, we dichotomized waist-to-height ratio at 0.512 (without considering the child's sex or age) so that the same proportion (17%) of children would be overweight and have a "high" waist-to-height ratio.
On each examination day, a 10% sample of the children was randomly selected to be reexamined 23 h later by the same observer. We use these data to compare the reproducibilities of BMI and waist-to-height ratio.
Risk factors
Concentrations of serum total cholesterol and triacylglycerols were measured by using enzymatic procedures in a centralized laboratory that met the requirements of the CDC's Lipid Standardization Program. For LDL- and HDL-cholesterol measurements, we used a combination of heparin-calcium precipitation and agar-agarose gel electrophoresis (27). Plasma insulin measurements were obtained with the use of a radioimmunoassay procedure (Phadebas Insulin Kit; Pharmacia Diagnostics AB, Uppsala, Sweden).
As previously described (23), sitting SBP and DBP in the right arm were measured 6 times by trained observers with a mercury sphygmomanometer (Baumanometer; WA Baum Co Inc, Copiague, NY). The cuff size was based on the length and circumference of the upper arm and was chosen to be as large as possible without having the elbow skin crease obstruct the stethoscope (28).
The distributions of lipid and lipoprotein concentrations in the Bogalusa Study were similar to those in the third National Health and Nutrition Examination (NHANES III) conducted from 1988 to 1994 (29). For example, the 90th percentiles of LDL cholesterol among 1215-y-old white children (data were not cross-classified by race, sex, or age group) in NHANES III were 122 mg/dL (whites) and 133 mg/dL (blacks); corresponding values in the Bogalusa Study were 127 mg/dL (whites) and 133 mg/dL (blacks). Similarly, the 10th percentiles of HDL cholesterol were 35 mg/dL (boys) and 36 mg/dL (girls) among 1215-y-olds in NHANES III and were 37 mg/dL among both boys and girls in the Bogalusa Study. However, because of differences in methods of measuring blood pressure (28), recorded measures of blood pressure are
510 mm Hg lower in the Bogalusa Study than in other studies.
Measures of adverse risk factors
Because measures of lipids, insulin, and blood pressures vary substantially by sex and age, we defined "adverse" measures in relation to a child's sex and age peers in the Bogalusa Study sample. After log-transformation of measures of the risk factors to improve normality, each risk factor was regressed on sex, race, and age. Age was modeled with the use of restricted cubic splines with 5 knots (see Statistical analyses) (30), and we allowed for interactions with age (age x BMI and age x waist-to-height ratio) in the prediction of each risk factor. Regression models for SBP and DBP also included height (cubic splines) as a predictor. The standardized residuals (adjusted risk factor measures) from these models represent measures relative to children of the same sex, race, and age. All adjusted risk factors had a mean ± SD value of 0 ± 1.0. With the exception of HDL cholesterol (<10th percentile), adverse risk factor measures were defined as a measure
90th percentile.
Although the identification of children with adverse risk factors in the current study is based solely on the distribution of risk factors in the Bogalusa Study, the use of cutoffs from NHANES III (29) identified similar children with adverse concentrations of lipids and lipoproteins. For example, all of the 1215-y-olds (whites and blacks combined; n = 106) in the current study who were classified as having a high LDL-cholesterol concentration (according to the Bogalusa Study cutoffs) also had a concentration >90th percentile (119 mg/dL) in NHANES III. However, 45 (5%) of the 950 children aged 1215 y who we considered to have a "normal" LDL-cholesterol concentration were in the >90th percentile in NHANES III. [It should be noted that some estimates of the 90th percentile in NHANES III were considered to be unstable because of the relatively small sample size (29).] Because of differences in methods of measuring blood pressure (28), few children in the Bogalusa Study had a SBP or DBP > 90th percentile of the National High Blood Pressure Education Program (31).
The risk factor sum was used as a summary measure of the 6 risk factors and was derived by combining adjusted measures of triacylglycerols, LDL cholesterol, HDL cholesterol, fasting insulin, SBP, and DBP. Adjusted measures of most risk factors were simply added together, but adjusted measures of HDL cholesterol were subtracted from the total. In addition, because of the high correlation (r = 0.66) between SBP and DBP, these 2 characteristics were first divided by 2. The resulting risk factor sum had a mean ±SD value of 0 ± 2.9 (range: 111). Correlations between the risk factor sum and the individual risk factors ranged from r = 0.37 (DBP) to r = 0.73 (triacylglycerols); the association with HDL cholesterol was r = 0.59.
The risk factor sum was highly correlated (r = 0.97) with the first principal component (32) of the 6 risk factors. Furthermore, with the exception of LDL-cholesterol concentrations (r = 0.39), the absolute value of the correlation coefficients with the first principal component ranged from 0.50 (HDL cholesterol) to 0.70 (triacylglycerols). (The second principal component was difficult to interpret because it contrasted measures of DBP, SBP, and HDL cholesterol with measures of triacylglycerols and fasting insulin, and it was not considered further.) Although risk factor summaries can be derived by adding together the number of adverse risk factors (16, 33), our method allows the risk factor sum to be used as a continuous variable.
Statistical analyses
The analyses, which were performed with the use of SAS software (version 9.1; SAS Institute Inc, Cary, NC) and R [version 2.4.1; R Foundation for Statistical Computing, Vienna, Austria (34)], first examined the ability of BMI-for-age and waist-to-height ratio to identify children with adverse measures of each risk factor. We calculated the positive predictive value (the proportion of children with a high BMI or waist-to-height ratio who actually have adverse risk factors) and the sensitivity (the proportion of children with adverse risk factors who have a high BMI or waist-to-height ratio) for each risk factor. Because these values depend on the cutoff used for BMI and waist-to-height ratio, we also examined the receiver operating characteristic curve for each risk factor. These curves are constructed by plotting the sensitivity at each value of BMI-for-age or waist-to-height ratio compared with the corresponding 1-specificity, and the area under the curve (AUC) quantifies the screening performance over all cutoffs. An AUC of 0.5 indicates that the screening test is no better than chance, and 1.0 indicates perfect classification. The statistical significance of the difference (35) in AUCs between BMI and waist-to-height ratio was calculated by using MEDCALC software (version 9.1.0.1; MedCalc Software, Mariakerke, Belgium).
Regression models were also used to quantify the prediction of risk factor measures by both indexes. (The original, unadjusted measures of the risk factors were used as the dependent variable in these models.) These analyses compared the increases in the multiple R2 values achieved by adding either BMI-for-age z score or waist-to-height ratio to a model already containing age, sex, and race. Continuous variables were modeled by using restricted cubic splines with 5 knots (30) to allow for nonlinearity, and we allowed for an interaction between each index and age. In contrast to the use of higher-order polynomials, models based on splines do not have peaks and valleys, and the fit in one region does not influence the fit in all other regions of the data.
To assess the differences between the R2 values of models that contained either BMI-for-age or waist-to-height ratio, we first calculated predicted risk factor measures from each model. We then examined the statistical significance of the difference in the correlation between the actual risk factor measures and the 2 sets of predicted risk factor measures coefficients (36). We also examined whether the relation of BMI-for-age and waist-to-height ratio to each risk factor was nonlinear.
We then cross-classified categories of BMI-for-age (<50th percentile, 50th84th percentile, 85th94th percentile, and
95th percentile) and waist-to-height ratio. Cutoffs for the 4 categories of waist-to-height ratio were selected so that the number of children in each category would equal the number in the corresponding BMI-for-age category. We focused on measures of the risk factor sum among children whose BMI-for-age stratum was lower or higher (discordant) than the corresponding waist-to-height ratio stratum. We also show the relation of waist-to-height ratio to BMI-for-age by using lowess to smooth the data (37).
In addition to determining whether differences between BMI-for-age and waist-to-height ratio were statistically significant, we also focused on the magnitudes of the differences in the AUCs and R2 values for each risk factor. It should be realized that a small difference between the 2 indexes, which indicates that their predictive abilities are similar, could be statistically significant. However, this small difference would have little practical importance.
| RESULTS |
|---|
|
|
|---|
|
11 y old). Although some differences were observed across strata (eg, the AUC for waist-to-height ratio was 0.87 among white children and 0.82 among black children), within each strata, the AUCs for BMI-for-age and waist-to-height ratio were almost identical.
|
|
|
= 0.21) was almost identical to the mean measure among children who had a high waist-to-height ratio relative to BMI-for-age (6 lower left cells;
= 0.19; P = 0.88). Comparable analyses for the individual risk factors indicated that children with a relatively high waist-to-height ratio had slightly higher concentrations of total cholesterol:HDL cholesterol and LDL cholesterol, whereas those with a high BMI-for-age had slightly higher concentrations of fasting insulin (P < 0.05 for each difference).
|
|
| DISCUSSION |
|---|
|
|
|---|
Various indexes of abdominal obesity (such as waist circumference, waist-to-hip ratio, and waist-to-height ratio) are associated with adverse risk factors among children (13-15) and are predictive of type 2 diabetes and CVD in adulthood (2-8). The limitations of these indexes, however, should be considered. For example, although waist circumference is correlated with the amount of intraabdominal visceral fat, which may be the most detrimental fat depot (9), it is also associated with subcutaneous abdominal fat and with total body fat (38, 39). In addition, a recent study of adults found that waist-to-height ratio and BMI were more strongly associated with each other (r = 0.850.91) than with percentage of body fat (r = 0.690.76), as determined by air-displacement plethysmography (19). These associations emphasize the potential problems in using waist-to-height ratio and BMI as indexes of abdominal and generalized adiposity, respectively. The interpretation of associations with BMI and waist-to-height ratio is further complicated by the possible relation of disease risk to height (40), which is in the denominator of both indexes.
Some investigators have concluded that, compared with BMI, waist-to-height ratio is more strongly associated with CVD risk factors among children (13-15) and adults (18, 19). It has been emphasized, however, that many of the differences between waist-to-height ratio and BMI are relatively small (19). For example, Hara et al (14) reported that the logarithm of a risk factor score showed correlations of r = 0.50 (waist-to-height ratio) and r = 0.45 (BMI), and Hsieh et al (33) reported correlations of r = 0.37 (waist-to-height ratio) and r = 0.33 (BMI) with a "morbidity index" among men. The slightly stronger relation of BMI-for-age (compared with waist-to-height ratio) to measures of SBP and DBP that we observed was also noted by others (15, 19).
Several explanations are possible for the contrasting findings about the relative importance of BMI-for-age and waist-to-height ratio. Various subsets of risk factors have been included in each study, and only one previous study included an index of insulin resistance (19). (Of the risk factors we examined, fasting insulin concentrations showed the strongest association with BMI.) Furthermore, a study of 36 obese children found that insulin resistance was more strongly associated with total fat mass than with visceral abdominal fat (41). The weaker associations with BMI that were found in previous studies of children may be due to the investigators' use of BMI rather than BMI-for-age (13, 14) or due to the fact that associations with BMI-for-age were constrained to be linear (14-16, 19). We found that forcing the association with concentrations of fasting insulin to be linear reduced the R2 for BMI-for-age from 0.48 (nonlinear) to 0.43 (linear), whereas the R2 for waist-to-height ratio decreased from 0.45 only to 0.44. These nonlinear associations may arise because BMI-for-age is a good indicator of adiposity among relatively fat children, but it is an index of both fat and fat-free mass among thinner children (42). If BMI-for-age differences among some relatively thin (eg, BMI-for-age z score < 1.0) children largely reflect differences in fat-free mass, it would be expected that the relation of BMI-for-age to risk factor measures would be "flatter" (Figure 1
) among these children.
The current study has several potential limitations that should be considered. Although the sample was not randomly selected, measures of BMI, lipids, and lipoproteins were fairly comparable to those reported in national studies (29). However, because of differences in methods of measuring blood pressure (28), few children in the Bogalusa Study had an SBP or a DBP > 90th percentile of the National High Blood Pressure Education Program (31). Furthermore, although it can be difficult to compare the magnitudes of the observed associations across studies because of differences in statistical modeling techniques, age ranges, and the specific anthropometric index examined, the magnitudes of the associations that we observed between BMI-for-age and the examined risk factors agree well with those of other studies (43).
Although several prospective studies found the indexes of abdominal obesity to be stronger predictors of CVD and type 2 diabetes than is BMI (4-7), there are conflicting findings. For example, the predictive abilities of BMI and waist-to-height ratio for type 2 diabetes among Pima Indians were almost identical (3), and several studies found that various indexes of abdominal obesity predict disease no better than does BMI (2, 8, 17). For example, the relative risk for coronary heart disease among men in the upper quintile of waist circumference in the Physicians' Health Study was 1.60, whereas the corresponding relative risk for BMI was 1.73 (8).
Some investigators have suggested that, even if the predictive abilities of waist-to-height ratio and BMI-for-age are similar, waist-to-height ratio may be preferred as an indicator of obesity-related risk (15, 21, 22). The concept of a large waist relative to height may be easier to explain than is the division of weight by the square of height, particularly for people accustomed to using pounds and inches. Furthermore, because waist-to-height ratios vary only slightly by age and by sex among children, it is not necessary to express measures as percentiles or z scores, relative to a reference population, as is the case for BMI. (The correlation between unadjusted and sex- and age-adjusted measures of waist-to-height ratio was r = 0.99, and the use of either adjusted or unadjusted measures yielded virtually identical results.) The calculation of waist-to-height ratio is also simpler, requiring only the division of numbers in the same units. Furthermore, the possible use of a single cutoff (0.5) to identify adverse measures among both children and adults (21) would result in a simple public health message: "Keep your waist circumference to less than half your height." In the current study, 85% of overweight children had a waist-to-height ratio
0.5.
However, the disease risks associated with BMI have been studied much more extensively than have those for waist-to-height ratio, and additional longitudinal data on waist-to-height ratio are needed. Furthermore, although the relation of childhood BMIs to those in adulthood was examined in numerous studies (reviewed in reference 44), we know of no study that has examined the tracking of waist-to-height ratios. In addition, although the reproducibility of waist circumference measurements is high (45), we and others have found that it is lower than that of BMI (19). This difference may limit the ability of waist-to-height ratio to detect small changes in obesity-related risk. Furthermore, waist circumference has been measured at numerous sites between the lowest rib and iliac crest, and there are differences between the recommendations of the Anthropometric Standardization Reference Manual (46), the World Health Organization, and the National Institutes of Health (reviewed in reference 45). Small changes in the location of the waist measurement can alter associations with risk factor measures (47-49) and possibly with disease risk.
In summary, we found that waist-to-height ratio and BMI-for-age showed similar associations with CVD risk factors. Although the use of waist-to-height ratio among children has the potential to simplify the assessment of obesity-related risk, additional information is needed on the tracking of waist-to-height ratio from childhood to adulthood, as are data relating waist-to-height ratio to morbidity and mortality.
| ACKNOWLEDGMENTS |
|---|
| REFERENCES |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
G. A Bray Reply to RJ Hine and JS White Am. J. Clinical Nutrition, April 1, 2008; 87(4): 1064 - 1065. [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |