Age-belated patterns of the clustering of cardiovascular risk variables ofSyndrome X from childhood to young adulthood in a population made up of black and white subjects - The Bogalusa Heart Study
W. Chen et al., Age-belated patterns of the clustering of cardiovascular risk variables ofSyndrome X from childhood to young adulthood in a population made up of black and white subjects - The Bogalusa Heart Study, DIABETES, 49(6), 2000, pp. 1042-1048
The age-related patterns of clustering of cardiovascular risk variables of
Syndrome X from childhood to adulthood were examined in a community-based s
ample of black and white children (aged 5-10 years, n = 2,389), adolescents
(aged 11-17 Sears, n = 3,371), and young adults (aged 18-37 years, n = 2,1
15). In the analysis of clustering, insulin resistance index, BMI, triglyce
rides/ HDL cholesterol ratio, and mean arterial pressure were used either a
s categorical variables (age-, race- and sex-specific values >75th percenti
les) to calculate risk ratios (observed frequency/expected frequency) or as
continuous variables (normal scores based on ranks) to compute intraclass
correlations. In the total sample, the risk ratio for clustering of adverse
levels of all 4 variables was 9.8 for whites (P < 0.01) versus 7.4 for bla
cks (P < 0.01); the intraclass correlation was 0.33 for whites (P < 0.001)
versus 0.26 for blacks (P < 0.001). Both the risk ratio and intraclass corr
elation were significantly higher in whites than in blacks in the total sam
ple. The intraclass correlations of the 3: variables were significant (P <
0.001) in all race and age-groups, and they were higher during preadolescen
ce and adulthood than during adolescence. Furthermore, unlike risk ratios,
intraclass correlations showed a continuous increase with age during adulth
ood. When BMI was adjusted, the intraclass correlations involving the other
3 variables were reduced by similar to 50%, and the age-related pattern ma
s no longer evident. These results suggest that the degree of clustering of
risk variables of Syndrome X varies with age from childhood to adulthood a
nd is likely influenced by the age-related changes in obesity and the atten
dant insulin resistance.