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Polycystic kidney disease

An early urea-selective urine-concentrating defect in ADPKD

A defect in urine-concentrating ability is discernable in patients with autosomal dominant polycystic kidney disease (ADPKD) before any decline in glomerular filtration rate, and is associated with elevated concentrations of vasopressin and copeptin. This defect is 'urea-selective' and accordingly, the urine-to-plasma ratio of urea concentration could be a clinically relevant early marker of renal dysfunction in patients with ADPKD.

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Figure 1: Urea handling in the renal medulla and its disturbance in patients with ADPKD.

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Correspondence to Lise Bankir.

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D. G. Bichet has worked as a consultant for Otsuka Pharmaceutical and received speakers bureau honoraria and grant/research support from Otsuka Pharmaceutical. L. Bankir declares no competing interests.

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Bankir, L., Bichet, D. An early urea-selective urine-concentrating defect in ADPKD. Nat Rev Nephrol 8, 437–439 (2012). https://doi.org/10.1038/nrneph.2012.139

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