Glucagon-stimulated copeptin measurements in the differential diagnosis of diabetes insipidus: a double-blind, randomized, placebo-controlled study

Author:

Atila Cihan12ORCID,Gaisl Odile12,Vogt Deborah R12,Werlen Laura2,Szinnai Gabor3,Christ-Crain Mirjam12ORCID

Affiliation:

1. Department of Endocrinology, Diabetology and Metabolism, University Hospital Basel , Basel, Switzerland

2. Department of Clinical Research, University Hospital Basel, University of Basel , Basel, Switzerland

3. Department of Paediatric Endocrinology and Diabetology, University Children's Hospital Basel , Basel, Switzerland

Abstract

Abstract Background The differential diagnosis of diabetes insipidus is challenging. The most reliable approaches are copeptin measurements after hypertonic saline infusion or arginine, which is a known growth hormone secretagogue but has recently also been shown to stimulate the neurohypophysis. Similar to arginine, glucagon stimulates growth hormone release, but its effect on the neurohypophysis is poorly studied. Design Double-blind, randomized, placebo-controlled trial including 22 healthy participants, 10 patients with central diabetes insipidus, and 10 patients with primary polydipsia at the University Hospital Basel, Switzerland. Methods Each participant underwent the glucagon test (s.c. injection of 1 mg glucagon) and placebo test. The primary objective was to determine whether glucagon stimulates copeptin and to explore whether the copeptin response differentiates between diabetes insipidus and primary polydipsia. Copeptin levels were measured at baseline, 30, 60, 90, 120, 150, and 180 min after injection. Results In healthy participants, glucagon stimulated copeptin with a median increase of 7.56 (2.38; 28.03) pmol/L, while placebo had no effect (0.10 pmol/L (−0.70; 0.68); P < 0.001). In patients with diabetes insipidus, copeptin showed no relevant increase upon glucagon, with an increase of 0.55 (0.21; 1.65) pmol/L, whereas copeptin was stimulated in patients with primary polydipsia with an increase of 15.70 (5.99; 24.39) pmol/L. Using a copeptin cut-off level of 4.6pmol/L had a sensitivity of 100% (95% CI: 100–100) and a specificity of 90% (95% CI: 70–100) to discriminate between diabetes insipidus and primary polydipsia. Conclusion Glucagon stimulates the neurohypophysis, and glucagon-stimulated copeptin has the potential for a safe, novel, and precise test in the differential diagnosis of diabetes insipidus.

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Reference24 articles.

1. Diabetes insipidus: differential diagnosis and management;Robertson;Best Practice and Research: Clinical Endocrinology and Metabolism,2016

2. Polyuria-polydipsia syndrome: a diagnostic challenge;Nigro;Internal Medicine Journal,2018

3. Copeptin in the differential diagnosis of the polydipsia-polyuria syndrome – revisiting the direct and indirect water deprivation tests;Fenske;Journal of Clinical Endocrinology and Metabolism,2011

4. Assay for the measurement of copeptin, a stable peptide derived from the precursor of vasopressin;Morgenthaler;Clinical Chemistry,2006

5. A copeptin-based approach in the diagnosis of diabetes insipidus;Fenske;New England Journal of Medicine,2018

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