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Published in: Clinical and Experimental Nephrology 3/2017

01-06-2017 | Original article

Polyuria due to vasopressin V2 receptor antagonism is not associated with increased ureter diameter in ADPKD patients

Authors: Niek F. Casteleijn, A. Lianne Messchendorp, Kyong T. Bae, Eiji Higashihara, Peter Kappert, Vicente Torres, Esther Meijer, Anna M. Leliveld

Published in: Clinical and Experimental Nephrology | Issue 3/2017

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Abstract

Background

Tolvaptan, a vasopressin V2 receptor antagonist, has been shown to reduce the rates of growth in total kidney volume (TKV) and renal function loss in ADPKD patients, but also leads to polyuria because of its aquaretic effect. Prolonged polyuria can result in ureter dilatation with consequently renal function loss. Therefore, we aimed to investigate the effect of tolvaptan-induced polyuria on ureter diameter in ADPKD patients.

Methods

70 ADPKD patients were included (51 were randomized to tolvaptan and 19 to placebo). At baseline and after 3 years of treatment renal function was measured (mGFR) and MRI was performed to measure TKV and ureter diameter at the levels of renal pelvis and fifth lumbar vertebral body (L5).

Results

In these patients [65.7 % male, age 41 ± 9 years, mGFR 74 ± 27 mL/min/1.73 m2 and TKV 1.92 (1.27–2.67) L], no differences were found between tolvaptan and placebo-treated patients in 24-h urine volume at baseline (2.5 vs. 2.5 L, p = 0.8), nor in ureter diameter at renal pelvis and L5 (4.0 vs. 4.2 mm, p = 0.4 and 3.0 vs. 3.1 mm, p = 0.3). After 3 years of treatment 24-h urine volume was higher in tolvaptan-treated patients when compared to placebo (4.7 vs. 2.3 L, p < 0.001), but no differences were found in ureter diameter between both groups (renal pelvis: 4.2 vs. 4.4 mm, p = 0.4 and L5: 3.1 vs. 3.3 mm, p = 0.4).

Conclusions

Tolvaptan-induced polyuria did not lead to an increase in ureter diameter, suggesting that tolvaptan is a safe therapy from a urological point of view.
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Metadata
Title
Polyuria due to vasopressin V2 receptor antagonism is not associated with increased ureter diameter in ADPKD patients
Authors
Niek F. Casteleijn
A. Lianne Messchendorp
Kyong T. Bae
Eiji Higashihara
Peter Kappert
Vicente Torres
Esther Meijer
Anna M. Leliveld
Publication date
01-06-2017
Publisher
Springer Japan
Published in
Clinical and Experimental Nephrology / Issue 3/2017
Print ISSN: 1342-1751
Electronic ISSN: 1437-7799
DOI
https://doi.org/10.1007/s10157-016-1297-1

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