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http://dx.doi.org/10.1056/NEJMc2314326 | DOI Listing |
Wilderness Environ Med
December 2024
University of Arizona College of Medicine, Phoenix, AZ, USA.
Nat Rev Nephrol
October 2024
Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.
Congenital nephrogenic diabetes insipidus (NDI; also known as arginine vasopressin resistance) is a rare inherited disorder of water homeostasis, caused by insensitivity of the distal nephron to arginine vasopressin. Consequently, the kidney loses its ability to concentrate urine, which leads to polyuria, polydipsia and the risk of hypertonic dehydration. The diagnosis and management of NDI are very challenging and require an integrated, multidisciplinary approach.
View Article and Find Full Text PDFEur J Endocrinol
October 2024
Department of Endocrinology, Diabetology and Metabolism, University Hospital Basel, Basel, Switzerland.
Objective: Differentiating between arginine vasopressin deficiency (AVP-D) and primary polydipsia (PP) requires a copeptin stimulation test. We aimed to characterize changes in apelin, an endogenous hormone antagonizing AVP, upon copeptin stimulation tests.
Design: Post hoc secondary analysis of a multi-centric cross-over diagnostic study (NCT03572166).
Int J Mol Sci
October 2024
Faculty of Medicine and Pharmacy, University "Dunarea de Jos" of Galati, 800201 Galati, Romania.
Endocr J
November 2024
Department of Diabetes and Endocrinology, Kanto Central Hospital of the Mutual Aid Association of Public School Teachers, Tokyo 158-8531, Japan.
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