ESPE2023 Poster Category 2 Pituitary, Neuroendocrinology and Puberty (28 abstracts)
1Vall d'Hebron University Hospital, Barcelona, Spain. 2Josep Trueta University Hospital, Girona, Spain
Introduction: Differential diagnosis of partial arginine vasopressin deficiency (P-AVPD) and primary polydipsia (PP) can be challenging. Arginine-stimulated copeptin concentrations have been used to differentiate between arginine vasopressin deficiency (AVPD) and PP, setting a copeptin value of 3.8pmol/L at 60 min as a cut-off point in adults.
Objective: To evaluate the efficacy and safety of the arginine-stimulated test in paediatrics.
Methods: Descriptive and prospective study on a diagnostic method in six paediatric patients with polydipsia-polyuria syndrome (PPS).
Inclusion criteria: Patients under 18 years with polyuria (>2mL/kg/h), normal glycaemia and no electrolytic changes. The arginine-copeptin test is performed with analytical control and vital signs (Times: basal, 0', 30', 60', 90', 120'). Patients description and results (Table 1 and 2): -Patient 1: 5-year-old boy with sudden PPS and MRI showing hypoplastic adenohypophysis and absence of neurohypophysis signal. Arginine-copeptin test <3.8pmol/L. -Patient 2: 12-year-old boy with long-standing PPS and syntelencephaly without alterations in the hypothalamic-pituitary region. Arginine-copeptin test >3.8pmol/L. -Patient 3: 13-year-old boy with sudden PPS. MRI showed an absence of the neurohypophysis and thickening of the pituitary stalk, etiological study pending. Arginine-copeptin test <3.8pmol/L. -Patient 4: 3-year-old girl with SGA, monosomy X, and Kabuki-like syndrome with long-standing PPS. MRI without alterations in the hypothalamic-pituitary axis. Arginine-copeptin test >3.8pmol/L. -Patient 5: 4-year-old girl with long-standing PPS. Arginine-copeptin test >3.8pmol/L. -Patient 6: 10-year-old boy with GH deficiency under treatment and MRI showing interruption of the pituitary stalk and ectopic neurohypophysis. He presents long-standing PPS. Arginine-copeptin test >3.8pmol/L. All patients were asymptomatic and hemodynamically stable during the procedure. Blood tests at the beginning and end of the test show no alterations.
1 | 2 | 3 | 4 | |
Duration (hours) | 15 | 17 | Basal (without restriction; plasma osmolality of 303mOsm/Kg) | 10 |
Urinary osmolarity before Desmopressin (mOsm/kg) | 601 | 495 | 98 | 304 |
Urinary osmolarity after Desmopressin (mOsm/kg) | 845 | 687 | 507 | 415 |
1 | 2 | 3 | 4 | 5 | 6 | |
Copeptin (pmol/L) | ||||||
Basal | 2,4 | 3,8 | 1,61 | 4.42 | 2.7 | 3,94 |
30’ | 2,5 | 4 | 1,48 | 5.24 | 3 | 5,3 |
60’ | 2,3 | 4,13 | 1,78 | 8.44 | 4.8 | 5,2 |
90’ | 1,8 | 3,8 | 1,98 | 4.5 | 6 | |
120’ | 2,4 | 1,47 | 9.72 | 3.7 | 5,8 | |
180’ | 3.7 | 4,5 | ||||
Diagnosis | P-AVPD | PP | AVPD | PP | PP | PP |
Conclusion: The arginine-stimulated copeptin test is a safe procedure and can represent an alternative to the diagnosis of AVPD.