Association between impaired fasting glycaemia in pediatric obesity and type 2 diabetes in young adulthood

E Hagman1, P Danielsson1, L Brandt2

  • 1Division of Pediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Nutrition & Diabetes
|August 23, 2016
PubMed

Insights

Children with obesity are significantly more likely to develop type 2 diabetes mellitus (T2DM). Impaired fasting glucose (IFG) and elevated hemoglobin A1c (HbA1c) in obese children are key risk markers for T2DM development.

Area of Science:

  • Endocrinology
  • Pediatrics
  • Metabolic Disorders

Background:

  • Obesity in children is a growing concern with long-term health implications.
  • Impaired fasting glucose (IFG) and elevated hemoglobin A1c (HbA1c) are known risk factors for type 2 diabetes mellitus (T2DM) in adults.
  • The predictive value of these markers in obese children transitioning to adulthood requires further investigation.

Purpose of the Study:

  • To assess the long-term risk of developing T2DM in individuals with a history of childhood obesity.
  • To determine if IFG and elevated HbA1c levels in obese children serve as early risk markers for T2DM.
  • To compare the predictive value of different IFG definitions (WHO vs. ADA) in this population.

Main Methods:

  • A prospective cohort study involving 1620 subjects from the Swedish Childhood Obesity Treatment Registry (BORIS) and 8046 matched controls.
  • IFG was defined using both American Diabetes Association (ADA) and World Health Organization (WHO) criteria.
  • Elevated HbA1c was defined by ADA criteria. T2DM diagnosis was determined by medication use from a national registry.

Main Results:

  • The childhood obesity cohort had a 24-fold increased likelihood of receiving T2DM medication in early adulthood compared to controls.
  • WHO-defined IFG (≥6.1 mmol/l) was a significant predictor of future T2DM medication use (adjusted HR=3.73).
  • Elevated HbA1c (≥39 mmol/l) also predicted T2DM medication use (adjusted HR=3.12), while the ADA-defined IFG interval (5.6-6.0 mmol/l) did not show significant predictive value beyond obesity itself.

Conclusions:

  • WHO-defined IFG and elevated HbA1c are significant prediabetes indicators in obese Swedish children.
  • The fasting glucose interval proposed by the ADA (5.6-6.0 mmol/l) is not a sufficient marker for prediabetes in this pediatric obese population.
  • These findings highlight the importance of early identification and management of metabolic risks in obese children to prevent T2DM.
Abstract

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