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Published on: January 7, 2018
Fasting Biomarkers and Glycated Haemoglobin Identify Children With Excess Weight at Risk of Dysglycaemia and Guide
Emre Sarıkaya1, Fatih Kilci1, Nurhan Özcan Murat1
1Department of Paediatric Endocrinology, Kocaeli City Hospital, Kocaeli, Türkiye.
Insights
Fasting biomarkers and HbA1c effectively identify children with excess weight who are at risk for dysglycaemia. These markers provide practical thresholds to guide the necessity of oral glucose tolerance testing (OGTT) for early intervention.
Area of Science:
- Pediatric Endocrinology
- Metabolic Health
- Obesity Research
Background:
- Childhood obesity is a significant public health concern.
- It is strongly linked to insulin resistance and dysglycaemia.
- Early identification of at-risk children is crucial for timely intervention.
Purpose of the Study:
- To evaluate fasting biomarkers and glycated haemoglobin (HbA1c).
- To identify children with excess weight at risk of dysglycaemia.
- To guide the need for oral glucose tolerance testing (OGTT).
Main Methods:
- A single-centre study of 475 children (aged 5-18 years) with excess weight.
- Fasting glucose (FG), fasting insulin (FI), HOMA-IR, HOMA-β, and HbA1c were assessed.
- Receiver operating characteristic (ROC) analysis determined optimal cut-offs for predicting dysglycaemia.
Main Results:
- 81.5% of children had insulin resistance and 18.9% had dysglycaemia.
- FG, FI, HOMA-IR, and HbA1c were significantly associated with dysglycaemia (p < 0.05).
- ROC analysis identified specific cut-offs for FG (5.27 mmol/L), HbA1c (39 mmol/mol), and HOMA-IR (4.88).
Conclusions:
- Fasting biomarkers and HbA1c are valuable tools for risk assessment in children with excess weight.
- Established thresholds can help clinicians decide on the need for OGTT.
- This approach supports personalized management of metabolic health in pediatric obesity.
Aim:
Childhood obesity has been strongly associated with insulin resistance and dysglycaemia. We aimed to evaluate fasting biomarkers and glycated haemoglobin (HbA1c) for identifying children at risk and guiding the need for oral glucose tolerance testing (OGTT).
Methods:
This single-centre study included 475 consecutive children aged 5-18 years with excess weight who underwent OGTT. Insulin resistance and dysglycaemia were defined based on OGTT-derived indices. Fasting glucose (FG), fasting insulin (FI), homeostatic model assessment of insulin resistance (HOMA-IR), homeostatic model assessment of β-cell function (HOMA-β), and HbA1c were evaluated. Receiver operating characteristic (ROC) analysis was used to determine optimal cut-offs for predicting dysglycaemia.
Results:
The cohort comprised 281 girls (59.2%) and 194 boys, with a median age of 13.8 years. Insulin resistance was present in 81.5% (387/475) and dysglycaemia in 18.9% (90/475). FG above the 90th percentile, FI and HOMA-IR above the 97.5th percentile, and HbA1c ≥ 39 mmol/mol (5.7%) were significantly associated with dysglycaemia (p < 0.05). ROC analysis for the entire cohort identified FG 5.27 mmol/L, HbA1c 39 mmol/mol, and HOMA-IR 4.88 as significant cut-offs (all p < 0.001).
Conclusion:
Fasting biomarkers and HbA1c identified children with excess weight at risk of dysglycaemia, providing practical thresholds to guide the need for OGTT.
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