Obesity and the development of insulin resistance and impaired fasting glucose in black and white adolescent girls - A longitudinal study

被引:47
作者
Klein, DJ
Friedman, LA
Harlan, WR
Barton, BA
Schreiber, GB
Cohen, RM
Harlan, LC
Morrison, JA
机构
[1] Childrens Hosp, Med Ctr, Div Cardiol, Cincinnati, OH 45229 USA
[2] Cincinnati Childrens Hosp, Med Ctr, Div Endocrinol & Cardiol, Cincinnati, OH USA
[3] Maryland Med Res Inst, Baltimore, MD USA
[4] NIMH, Bethesda, MD 20892 USA
[5] WESTAT Corp, Rockville, MD 20850 USA
[6] Univ Cincinnati, Dept Internal Med, Div Endocrinol, Cincinnati, OH USA
[7] NCI, Bethesda, MD 20892 USA
关键词
D O I
10.2337/diacare.27.2.378
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Age at onset of type 2 diabetes has decreased during the past 20 years, especially in black women. Studies of factors associated with insulin resistance and hyperglycemia in preadolescent and adolescent populations are essential to understanding diabetes development. Research Design and Methods-The National Heart, Lung, and Blood Institute (NHLBI) Growth and Health Study (NGHS) is a 10-year cohort study of the development of obesity in black and white girls. Two NGHS centers examined the associations of obesity, puberty, and race with fasting insulin, glucose, and homeostasis model assessment of insulin resistance (HOMA-IR; a calculated index of insulin resistance) measures at 9-10 years of age (baseline) and 10 years later. Results-Black girls had greater baseline and year-10 BMI than white girls, with a greater 10-year incidence of obesity. BMI-insulin correlations were positive in both black and white girls at both visits, but insulin remained higher in black girls after controlling for BMI. In black girls, insulin and HOMA-IR were higher in the prepubertal period (before the emergence of racial differences in BMI), increased more during puberty, and decreased less with its completion. Baseline BMI predicted year-10 glucose and the development of impaired fasting glucose (IFG) in black girls. In white girls, the rate of BMI increase during follow-up predicted these outcomes. The 10-year incidence of diabetes in black girls was 1.4%. Conclusions-Black-white differences in insulin resistance are not just a consequence of obesity, but precede the pubertal divergence in BMI. The development of IFG appears to be a function of the rate of increase of BMI in white girls and early obesity in black girls.
引用
收藏
页码:378 / 383
页数:6
相关论文
共 26 条
[1]   Insulin secretion and sensitivity in black versus white prepubertal healthy children [J].
Arslanian, S ;
Suprasongsin, C ;
Janosky, JE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (06) :1923-1927
[2]   Hyperinsulinemia in African-American children - Decreased insulin clearance and increased insulin secretion and its relationship to insulin sensitivity [J].
Arslanian, SA ;
Saad, H ;
Lewy, V ;
Danadian, K ;
Janosky, J .
DIABETES, 2002, 51 (10) :3014-3019
[3]  
Association AD, 2002, DIABETES CARE, V25, ps21, DOI [DOI 10.2337/DIACARE.25.2007.S21, 10.2337/diacare.25.2007.S21]
[4]   Obesity evaluation and treatment: Expert committee recommendations [J].
Barlow, SE ;
Dietz, WH .
PEDIATRICS, 1998, 102 (03)
[5]   AREOLAR AND BREAST STAGING IN ADOLESCENT GIRLS [J].
BIRO, FM ;
FALKNER, F ;
KHOURY, P ;
MORRISON, JA ;
LUCKY, AW .
ADOLESCENT AND PEDIATRIC GYNECOLOGY, 1992, 5 (04) :271-272
[6]   Co-existence of severe insulin resistance and hyperinsulinaemia in pre-adolescent obese children [J].
Caprio, S ;
Bronson, M ;
Sherwin, RS ;
Rife, F ;
Tamborlane, WV .
DIABETOLOGIA, 1996, 39 (12) :1489-1497
[7]  
COLE T. J., 1991, ANTHROPOMETRIC ASSES, P83
[8]   DURATION OF OBESITY INCREASES THE INCIDENCE OF NIDDM [J].
EVERHART, JE ;
PETTITT, DJ ;
BENNETT, PH ;
KNOWLER, WC .
DIABETES, 1992, 41 (02) :235-240
[9]   Longitudinal study on pubertal insulin resistance [J].
Goran, MI ;
Gower, BA .
DIABETES, 2001, 50 (11) :2444-2450
[10]   Contribution of insulin secretion and clearance to glucose-induced insulin concentration in African-American and Caucasian children [J].
Gower, BA ;
Granger, WM ;
Franklin, F ;
Shewchuk, RM ;
Goran, MI .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (05) :2218-2224