Reversal of Early Abnormalities in Glucose Metabolism in Obese Youth: Results of an Intensive Lifestyle Randomized Controlled Trial
- Mary Savoye1,2⇑,
- Sonia Caprio1,
- James Dziura3,
- Anne Camp4,
- Greg Germain5,
- Craig Summers6,
- Fangyong Li7,
- Melissa Shaw1,
- Paulina Nowicka8,
- Romy Kursawe1,
- Fredrick DePourcq2,
- Grace Kim1 and
- William V. Tamborlane1
- 1Pediatric Endocrinology, Yale University School of Medicine, New Haven, CT
- 2Yale Center for Clinical Investigation, New Haven, CT
- 3Department of Emergency Medicine, Yale University School of Medicine, New Haven, CT
- 4Fair Haven Community Health Center, New Haven, CT
- 5Pediatric and Medical Associates, New Haven, CT
- 6Children’s Medical Group, Hamden, CT
- 7Yale Center for Analytical Sciences, School of Public Health, New Haven, CT
- 8Division of Pediatrics, Department of Clinical Science, Intervention, and Technology, Karolinska Institute, Stockholm, Sweden
- Corresponding author: Mary Savoye, .
OBJECTIVE The childhood obesity epidemic has been accompanied by an increasing prevalence of type 2 diabetes (T2D), particularly in minority children. Twenty to thirty percent of obese youth have “prediabetes,” a precursor to diabetes marked by insulin resistance, β-cell dysfunction, and impaired glucose tolerance. The Diabetes Prevention Program demonstrated that T2D could be prevented/delayed by intensive lifestyle modification in adults with prediabetes, but efficacy of similar interventions in youth has not been established. Therefore, we evaluated the effects of the Bright Bodies (BB) Healthy Lifestyle Program on 2-h oral glucose tolerance test (OGTT) glucose in comparison with adolescents receiving standard of care.
RESEARCH DESIGN AND METHODS A parallel-group randomized controlled trial comparing BB with standard clinical care (CC) in obese adolescents (10–16 years old, Tanner stage >2) with elevated OGTT 2-h blood glucose (130–199 mg/dL) from a racially/ethnically diverse population. OGTTs, including cardiovascular and anthropometric assessments, were conducted at baseline and 6 months. Children attended BB twice per week for exercise and nutrition/behavior modification, and the CC group received CC from their pediatrician. Primary outcome was change in 2-h OGTT glucose and percentage conversion from elevated 2-h blood glucose to nonelevated (<130 mg/dL) 2-h blood glucose. Changes in outcomes were compared between groups using an ANCOVA, with adjustment for baseline outcome and multiple imputation for missing data.
RESULTS Reductions in 2-h glucose were more favorable in BB compared with CC (−27.2 vs. −10.1 mg/dL; difference = −17.1, 95% CI; P = 0.005). Moreover, greater conversion to <130 mg/dL 2-h glucose occurred in BB than CC (P = 0.003), and other insulin sensitivity indices were significantly improved.
CONCLUSIONS Compared with standard of care, the Yale BB Program is a more effective means of reducing the risk of T2D in obese adolescents with elevated 2-h glucose levels.
This article contains Supplementary Data online at http://care.diabetesjournals.org/lookup/suppl/doi:10.2337/dc13-1571/-/DC1.
- Received July 3, 2013.
- Accepted August 31, 2013.
- © 2014 by the American Diabetes Association.
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