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Home urine C-peptide creatinine ratio (UCPCR) testing can identify type 2 and MODY in pediatric diabetes
Rachel E J Besser1, Beverley M Shields, Suzanne E Hammersley
1Peninsula NIHR Clinical Research Facility, Peninsula Medical School, University of Exeter, Exeter, UK. rachel.besser@nhs.net
Insights
Postprandial urinary C-peptide creatinine ratio (UCPCR) effectively distinguishes type 1 diabetes from type 2 and MODY in children over two years duration. This non-invasive test aids in accurate pediatric diabetes diagnosis.
Area of Science:
- Pediatric Endocrinology
- Diabetes Diagnostics
- Metabolic Disorders
Background:
- Accurate diabetes diagnosis in children is vital for lifelong management.
- Differentiating type 1 diabetes from type 2 and MODY in pediatric patients presents diagnostic challenges.
- Postprandial urinary C-peptide creatinine ratio (UCPCR) is an underutilized non-invasive measure of insulin secretion.
Purpose of the Study:
- To evaluate the utility of UCPCR in differentiating pediatric diabetes subtypes.
- To assess UCPCR as a diagnostic tool in children with diabetes duration less than 5 years.
- To determine if UCPCR can distinguish type 1 diabetes from MODY and type 2 diabetes in pediatric populations.
Main Methods:
- Measured 2-hour postprandial UCPCR in 264 pediatric patients (<21 years) with type 1 diabetes (n=160), type 2 diabetes (n=41), and MODY (n=63).
- Employed receiver operating characteristic (ROC) curve analysis to establish optimal UCPCR cutoffs for subtype discrimination.
- Analyzed UCPCR values in relation to diabetes type and duration of disease.
Main Results:
- UCPCR was significantly lower in type 1 diabetes compared to type 2 diabetes and MODY (p<0.0001).
- UCPCR values were similar between type 2 diabetes and MODY (p=0.25).
- For diabetes duration >2 years, UCPCR ≥ 0.7 nmol/mmol demonstrated 100% sensitivity and 97% specificity in identifying non-type 1 diabetes (MODY + type 2) from type 1 diabetes (AUC 0.997).
Conclusions:
- UCPCR testing is a practical, non-invasive method for identifying non-type 1 diabetes in pediatric patients with diabetes duration exceeding 2 years.
- UCPCR can reliably differentiate type 1 diabetes from other forms in the pediatric outpatient setting.
- UCPCR showed limited ability to discriminate between MODY and type 2 diabetes.
Background:
Making the correct diabetes diagnosis in children is crucial for lifelong management. Type 2 diabetes and maturity onset diabetes of the young (MODY) are seen in the pediatric setting, and can be difficult to discriminate from type 1 diabetes. Postprandial urinary C-peptide creatinine ratio (UCPCR) is a non-invasive measure of endogenous insulin secretion that has not been tested as a diagnostic tool in children or in patients with diabetes duration <5 yr. We aimed to assess whether UCPCR can discriminate type 1 diabetes from MODY and type 2 in pediatric diabetes.
Methods:
Two-hour postprandial UCPCR was measured in 264 patients aged <21 yr (type 1, n = 160; type 2, n = 41; and MODY, n = 63). Receiver operating characteristic curves were used to identify the optimal UCPCR cutoff for discriminating diabetes subtypes.
Results:
UCPCR was lower in type 1 diabetes [0.05 (<0.03-0.39) nmol/mmol median (interquartile range)] than in type 2 diabetes [4.01 (2.84-5.74) nmol/mmol, p < 0.0001] and MODY [3.51 (2.37-5.32) nmol/mmol, p < 0.0001]. UCPCR was similar in type 2 diabetes and MODY (p = 0.25), so patients were combined for subsequent analyses. After 2-yr duration, UCPCR ≥ 0.7 nmol/mmol has 100% sensitivity [95% confidence interval (CI): 92-100] and 97% specificity (95% CI: 91-99) for identifying non-type 1 (MODY + type 2 diabetes) from type 1 diabetes [area under the curve (AUC) 0.997]. UCPCR was poor at discriminating MODY from type 2 diabetes (AUC 0.57).
Conclusions:
UCPCR testing can be used in diabetes duration greater than 2 yr to identify pediatric patients with non-type 1 diabetes. UCPCR testing is a practical non-invasive method for use in the pediatric outpatient setting.
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