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Glucagon-stimulated copeptin response in children: a proof-of-concept study
Rita Indirli1,2, Federico Giacchetti1, Eriselda Profka1,2
1Endocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy.
Insights
The glucagon stimulation test (GST) effectively increases copeptin levels in children, showing promise for diagnosing polyuria-polydipsia syndrome (PPS). Further research is needed to confirm its diagnostic accuracy in pediatric cases.
Area of Science:
- Pediatric Endocrinology
- Diagnostic Testing
- Hormone Assays
Background:
- The diagnostic workup for polyuria-polydipsia syndrome (PPS) in children is not well-established.
- Non-osmotic copeptin-stimulating agents are being investigated for PPS diagnosis.
- Glucagon stimulation test (GST) shows a robust copeptin response in adults, but data in children are lacking.
Purpose of the Study:
- To investigate the copeptin response to the glucagon stimulation test (GST) in children.
- To evaluate GST's potential in diagnosing growth hormone (GH) deficiency and PPS in pediatric patients.
Main Methods:
- Twenty children (9 girls, mean age 10.3 years) without PPS underwent GST.
- Plasma glucose, GH, cortisol, and copeptin levels were measured pre- and post-glucagon injection at multiple time points.
Main Results:
- GST induced a significant increase in copeptin levels, with peak concentration at 150 minutes (+87%).
- Median copeptin increased from 4.1 pmol/L at baseline to 10.6 pmol/L at peak.
- No adverse events were reported during the GST procedure.
Conclusions:
- GST is a safe and effective method for stimulating copeptin secretion in children with normal neurohypophysial function.
- Further studies are warranted to establish GST's accuracy in the differential diagnosis of pediatric PPS.
Purpose:
The diagnostic workup of polyuria-polydipsia syndrome (PPS) is not well-established in children and adolescents, and several non-osmotic copeptin-stimulating agents have been investigated. Glucagon stimulation test (GST) induced a robust copeptin response in adults, but data in children are lacking. This study aimed to investigate copeptin response to GST in children tested for suspected growth hormone (GH) deficiency.
Methods:
Twenty children (9 girls, age 10.3 ± 2.9 years) with no PPS underwent GST (30 µg/kg of glucagon i.m.). Plasma glucose, GH, cortisol, and copeptin were measured before and 60, 90, 120, 150, and 180 min after glucagon injection.
Results:
Median copeptin concentration was 4.1 pmol/L (IQR 3.3-6.7) at baseline and 10.6 pmol/L (5.4-17.9) at peak concentration (+87% at 150 min). No adverse events were recorded.
Conclusion:
GST is safe and effective at enhancing copeptin secretion in children with intact neurohypophysial function, and further studies are warranted to assess its accuracy in the differential diagnosis of PPS.
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