Key result
Novel C-peptide-glucose index detects pediatric insulin resistance with ~87% sensitivity.
Why the study?
Does the 20/ (fasting C-peptide × fasting plasma glucose) index accurately detect insulin resistance in obese children and adolescents?
Case-Control (n=100)
Does the 20/ (fasting C-peptide × fasting plasma glucose) index accurately detect insulin resistance in obese children and adolescents?
Answers are grounded in this paper and cite their sources.
The 20/ (fasting C-peptide × fasting plasma glucose) index is a promising and reliable surrogate marker for detecting insulin resistance in obese children and adolescents.
Background Insulin resistance (IR) constitutes a critical pathophysiological mechanism linking pediatric obesity to type 2 diabetes mellitus (T2DM) and cardiovascular disease. Recent investigations in adult populations have proposed 20/ fasting C-peptide × fasting plasma glucose (20/ (Fcpep X FBG)) as a good biomarker for IR. We aimed to evaluate the diagnostic utility of this novel index in detecting IR among obese pediatric patients. Methods This case-control study included 100 children (50 obese and 50 controls), aged 6–16 years. Anthropometric, clinical, and laboratory assessments were performed, including fasting blood glucose, fasting serum insulin, fasting C-peptide, and lipid profile. IR was evaluated using HOMA-IR, HbA1c, TyG index, and 20/ (Fcpep X FBG). Results Obese children demonstrated significantly elevated metabolic parameters, including body mass index (BMI), HOMA-IR, and fasting C-peptide. The (20/Fcpep x FBG) index was significantly lower in obese subjects (0.10 ± 0.04 vs. 0.18 ± 0.05, p < 0.001) and exhibited strong inverse correlations with HOMA-IR, BMI, TyG index, and HbA1c. 20/ Fcpep X FBG can significantly predict IR at a cut-off ≤0.164 with 86.67% sensitivity, 85% specificity. Conclusions The 20/ (Fcpep X FBG) index represents a convenient and accurate biomarker for IR detection in obese pediatric populations, demonstrating robust correlations with established metabolic indicators. Impact Insulin resistance (IR) constitutes a critical pathophysiological mechanism linking pediatric obesity to type 2 diabetes mellitus (T2DM) and cardiovascular disease. Homeostatic model assessment of insulin resistance (HOMA-IR) and Triglyceride glucose (TyG) index serve as the established surrogate markers; recent investigations in adult populations have proposed 20/ fasting C-peptide × fasting plasma glucose (20/ (Fcpep X FBG) as a superior alternative. However, its utility in pediatric patients with obesity has not been evaluated. We found that the (20/ (Fcpep X FBG) is a promising and reliable marker for detecting IR in obese children and adolescents.
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Amrousy et al. (2026) conducted a case-control in Obesity and Insulin Resistance (n=100). Obesity vs. Healthy controls was evaluated on 20/ (fasting C-peptide × fasting plasma glucose) index (p=< 0.001). The 20/ (fasting C-peptide × fasting plasma glucose) index was lower in obese children than controls and predicted insulin resistance with 86.67% sensitivity.
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