Vitamin D Supplementation Does Not Impact Insulin Resistance in Black and White Children

被引:23
作者
Ferira, Ashley J. [1 ]
Laing, Emma M. [1 ]
Hausman, Dorothy B. [1 ]
Hall, Daniel B. [2 ]
McCabe, George P. [4 ]
Martin, Berdine R. [3 ]
Gallant, Kathleen M. Hill [3 ]
Warden, Stuart J. [6 ]
Weaver, Connie M. [3 ]
Peacock, Munro [5 ]
Lewis, Richard D. [1 ]
机构
[1] Univ Georgia, Dept Foods & Nutr, Athens, GA 30602 USA
[2] Univ Georgia, Dept Stat, Athens, GA 30602 USA
[3] Purdue Univ, Dept Nutr Sci, W Lafayette, IN 47907 USA
[4] Purdue Univ, Dept Stat, W Lafayette, IN 47907 USA
[5] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
[6] Indiana Univ, Sch Hlth & Rehabil Sci, Dept Phys Therapy, Indianapolis, IN 46202 USA
关键词
CARDIOMETABOLIC RISK-FACTORS; SERUM 25-HYDROXYVITAMIN D; BETA-CELL FUNCTION; FOOD FREQUENCY QUESTIONNAIRE; FASTING PLASMA-GLUCOSE; METABOLIC SYNDROME; OBESE ADOLESCENTS; US CHILDREN; SENSITIVITY; HOMEOSTASIS;
D O I
10.1210/jc.2015-3687
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Vitamin D supplementation trials with diabetes-related outcomes have been conducted almost exclusively in adults and provide equivocal findings. Objective: The objective of this study was to determine the dose-response of vitamin D supplementation on fasting glucose, insulin, and a surrogate measure of insulin resistance in white and black children aged 9-13 years, who participated in the Georgia, Purdue, and Indiana University (or GAPI) trial: a 12-week multisite, randomized, triple-masked, dose-response, placebo-controlled vitamin D trial. Design: Black and white children in the early stages of puberty (N = 323, 50% male, 51% black) were equally randomized to receive vitamin D3 (0, 400, 1000, 2000, or 4000 IU/day) for 12 weeks. Fasting serum 25-hydroxyvitamin D (25(OH)D), glucose and insulin were assessed at baseline and weeks 6 and 12. Homeostasis model assessment of insulin resistance was used as a surrogate measure of insulin resistance. Statistical analyses were conducted as intent-to-treat using a mixed effects model. Results: Baseline serum 25(OH)D was inversely associated with insulin (r = -0.140, P = 0.017) and homeostasis model assessment of insulin resistance (r = -0.146, P = 0.012) after adjusting for race, sex, age, pubertal maturation, fat mass, and body mass index. Glucose, insulin, and insulin resistance increased (F > 5.79, P < .003) over the 12 weeks, despite vitamin D dose-dependent increases in serum 25(OH)D. Conclusions: Despite significant baseline inverse relationships between serum 25(OH)D and measures of insulin resistance, vitamin D supplementation had no impact on fasting glucose, insulin, or a surrogate measure of insulin resistance over 12 weeks in apparently healthy children.
引用
收藏
页码:1710 / 1718
页数:9
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