Path analysis of metabolic syndrome components in black versus white children, adolescents, and adults: The bogalusa heart study

被引:36
作者
Chen, Wei [1 ,2 ]
Srinivasan, Sathanur R. [1 ,2 ]
Berenson, Gerald S. [1 ,2 ]
机构
[1] Tulane Univ, Tulane Ctr Cardiovasc Hlth, New Orleans, LA 70118 USA
[2] Tulane Univ, Dept Epidemiol, New Orleans, LA 70118 USA
关键词
metabolic syndrome x; obesity; insulin resistance;
D O I
10.1016/j.annepidem.2007.07.090
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
PURPOSE: Examine the complex relationships among metabolic syndrome components in black and white individuals by growth periods. METHODS: Path analyses of metabolic syndrome components were performed on 8203 black and white healthy subjects (64.3% white and 47.9% male) comprising children (4-11 years), adolescents (12-18 years), and adults (19-44 years). RESULTS: The direct effect of body mass index (BMI) on fasting insulin levels was greatest among all the paths for each age group in both races. In general, path coefficients were greater in whites than in blacks except for the age-mean arterial pressure (MAP) path and greater in children and adults than in adolescents. The direct age effect on MAP was greater in black versus white adults (p = 0.010 for race difference). Whites showed greater direct effects of BMI on MAP in children (p = 0.007), adolescents (p = 0.090), and adults (p = 0.022); BMI on insulin in adolescents (p < 0.001); BMI on triglycerides in children (p = 0.003); and insulin on triglycerides in adults (p < 0.001). A race difference in the effect of BMI on fasting glucose was noted among adolescents (p = 0.048). CONCLUSIONS: The black-white differences in the relationships of obesity and insulin resistance measures to other components may account for the lower prevalence of metabolic syndrome in the black population.
引用
收藏
页码:85 / 91
页数:7
相关论文
共 49 条
[21]  
Joreskog K, 1993, LISREL 8 52 STRUCTUR
[22]   Associations between weight gain and incident hypertension in a bi-ethnic cohort: the Atherosclerosis Risk in Communities Study [J].
Juhaeri ;
Stevens, J ;
Chambless, LE ;
Tyroler, HA ;
Rosamond, W ;
Nieto, FJ ;
Schreiner, P ;
Jones, DW ;
Arnett, D .
INTERNATIONAL JOURNAL OF OBESITY, 2002, 26 (01) :58-64
[23]   The metabolic syndrome: Time for a critical appraisal - Joint statement from the American Diabetes Association and the European Association for the Study of Diabetes [J].
Kahn, R ;
Buse, J ;
Ferrannini, E ;
Stern, M .
DIABETES CARE, 2005, 28 (09) :2289-2304
[24]  
KOTCHEN JM, 1982, HYPERTENSION, V4, P128
[25]   The metabolic syndrome and total and cardiovascular disease mortality in middle-aged men [J].
Lakka, HM ;
Laaksonen, DE ;
Lakka, TA ;
Niskanen, LK ;
Kumpusalo, E ;
Tuomilehto, J ;
Salonen, JT .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (21) :2709-2716
[26]   PUBERTY IN BOYS - CORRELATION OF PLASMA-LEVELS OF GONADOTROPINS (LH, FSH), ANDROGENS (TESTOSTERONE, ANDROSTENEDIONE, DEHYDROEPIANDROSTERONE AND ITS SULFATE), ESTROGENS (ESTRONE AND ESTRADIOL) AND PROGESTINS (PROGESTERONE AND 17-HYDROXYPROGESTERONE) [J].
LEE, PA ;
MIGEON, CJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1975, 41 (03) :556-562
[27]   PUBERTY IN GIRLS - CORRELATION OF SERUM LEVELS OF GONADOTROPINS, PROLACTIN, ANDROGENS, ESTROGENS, AND PROGESTINS WITH PHYSICAL CHANGES [J].
LEE, PA ;
XENAKIS, T ;
WINER, J ;
MATSENBAUGH, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1976, 43 (04) :775-784
[28]  
Li C.C., 1975, PATH ANAL PRIMER
[29]   Development of the multiple metabolic syndrome: An epidemiologic perspective [J].
Liese, AD ;
Mayer-Davis, EJ ;
Haffner, SM .
EPIDEMIOLOGIC REVIEWS, 1998, 20 (02) :157-172
[30]   LONGITUDINAL ASSESSMENT OF BLOOD PRESSURES IN BLACK-AND-WHITE CHILDREN [J].
MANATUNGA, AK ;
JONES, JJ ;
PRATT, JH .
HYPERTENSION, 1993, 22 (01) :84-89