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Urinary C-peptide creatinine ratio to differentiate type 2 diabetes mellitus from type 1 in pediatric patients
Wafaa Elzahar1, Ahmed Arafa1, Amira Youssef2
1Pediatric Department, Faculty of Medicine, Tanta University Hospital, El motasem street No 6, Tanta, Egypt.
Insights
Urinary C-peptide to creatinine ratio (UCPCR) effectively distinguishes type 2 diabetes mellitus (T2DM) from type 1 DM (T1DM) in children. This noninvasive marker shows high sensitivity and specificity, aiding accurate pediatric diabetes diagnosis.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Diabetes Research
Background:
- Type 2 diabetes mellitus (T2DM) is often misdiagnosed in children as type 1 DM (T1DM), leading to inappropriate insulin treatment.
- Urinary C-peptide to creatinine ratio (UCPCR) is a validated measure of pancreatic beta-cell function and endogenous insulin production.
Purpose of the Study:
- To evaluate the diagnostic utility of UCPCR in differentiating T2DM from T1DM in pediatric patients.
- To establish an optimal UCPCR cutoff value for distinguishing between T1DM and T2DM in children.
Main Methods:
- Assessed UCPCR from post-lunch urine samples in 50 children with T1DM and 30 with T2DM (disease duration ≥2 years, no renal impairment).
- Measured fasting and postprandial C-peptide levels in all participants.
- Utilized Receiver Operating Characteristic (ROC) curve analysis to determine the optimal UCPCR cutoff.
Main Results:
- UCPCR levels were significantly lower in children with T1DM compared to those with T2DM (P < 0.001).
- UCPCR demonstrated high diagnostic accuracy, with a sensitivity of 97% and specificity of 88% at a cutoff of ≥0.28 nmol/nmol.
- Significant correlations were observed between UCPCR and C-peptide levels, age of onset, HbA1c, and DM duration.
Conclusions:
- UCPCR serves as a reliable, noninvasive, and easily accessible biomarker for differentiating T2DM from T1DM in pediatric populations.
- The established UCPCR cutoff value aids in accurate diagnosis, potentially improving treatment strategies for children with diabetes.
Abstract:
Type 2 diabetes mellitus (T2DM) is frequently misdiagnosed in children and treated as type 1 DM (T1DM) with insulin. Urinary C-peptide to creatinine ratio (UCPCR) can be used to measure ß cell function and endogenous insulin. We aimed to assess the value of UCPCR to differentiate T2DM from T1DM in pediatric patients. We assessed UCPCR from urine sample taken 2 h after lunch in 50 children with T1DM and 30 children with T2DM (duration of the disease ≥ 2 years and without renal impairment). Fasting and postprandial C-peptide levels were also evaluated in all included children. Receiver operating characteristic (ROC) curve was performed to assess the optimal UCPCR cutoff level to differentiate T2DM from T1DM in children. UCPCR was significantly lower in children with T1DM compared with those with T2DM (P < 0.001). There was a significant positive correlation between UCPCR and fasting C-peptide, postprandial C-peptide, and age of onset. There was a significant negative correlation between the UCPCR and both HbA1c and duration of DM in T1DM. Fasting C-peptide had a sensitivity of 63%, a specificity of 84% at a cutoff point ≥ 1.3 ng/ml to differentiate T2DM from T1DM. Postprandial C-peptide had a sensitivity of 87%, a specificity of 86% at a cutoff point ≥ 3.2 ng/ml to differentiate T2DM from T1DM. Finally, UCPCR had a sensitivity of 97%, a specificity of 88% at a cutoff point ≥ 0.28 nmol/nmol to differentiate T2DM from T1DM in pediatric patients.Conclusion: UCPCR is an easy noninvasive reliable marker to differentiate T2DM from T1DM in pediatric patients.What is Known:• Type 2 DM (T2DM) is frequently misdiagnosed in children and treated as type 1 DM (T1DM) with insulin.• Urinary C-peptide to creatinine ratio (UCPCR) can be used to measure ß cell function and endogenous insulin.What is New:• We revealed that UCPCR had a sensitivity of 97%, a specificity of 88% at a cutoff point ≥ 0.28 nmol/nmol to differentiate T2DM from T1DM.• UCPCR is an easy noninvasive dependable marker to diagnose T2DM from T1DM in pediatric patients.
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