Congenital and acquired nephrogenic diabetes insipidus: Diagnostic and therapeutic update [Diabetes insípida nefrogénica congénita y adquirida: Actualización diagnóstica y terapéutica]

Authors

DOI:

https://doi.org/10.62574/hxe96t68

Keywords:

diabetes insipidus nephrogenic, vasopressins, aquaporin 2

Abstract

Objective: To review current literature on pathophysiology, diagnosis and treatment of nephrogenic diabetes insipidus, improving clinical understanding and management. Materials and methods: A systematic review was conducted in PubMed, SciELO, ScienceDirect and Google Scholar, including articles published between 2020-2025. Terms such as nephrogenic diabetes insipidus, vasopressin, diagnosis and treatment were used. Results: Incidence is 1 in 100,000-250,000 people. 90% of congenital cases are due to AVPR2 mutations, predominantly affecting males. Lithium causes renal resistance to vasopressin in 40-55% of long-term treated patients. Diagnosis is based on elevated plasma osmolality, low urinary osmolality and absence of desmopressin response. Conclusions: Early diagnosis through clinical evaluation and renal function tests is crucial. Treatment includes adequate hydration, low-sodium diet, thiazides and NSAIDs, improving quality of life.

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References

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Published

2025-10-20

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Originales breves

How to Cite

1.
Valencia-Herrera AR, Moscoso-Estrella MA, Morales-Andino DG. Congenital and acquired nephrogenic diabetes insipidus: Diagnostic and therapeutic update [Diabetes insípida nefrogénica congénita y adquirida: Actualización diagnóstica y terapéutica]. CER [Internet]. 2025 Oct. 20 [cited 2026 Jul. 27];3(especial2):47-53. Available from: https://revistasinstitutoperspectivasglobales.rperspectivasinvestigativas.org/index.php/CER/article/view/895

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