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

TitlePolyuria due to vasopressin V2 receptor antagonism is not associated with increased ureter diameter in ADPKD patients
Authors
KeywordsAutosomal dominant polycystic kidney disease
Polyuria
Tolvaptan
Ureter
Issue Date2017
Citation
Clinical and Experimental Nephrology, 2017, v. 21, n. 3, p. 375-382 How to Cite?
AbstractBackground: 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.
Persistent Identifierhttp://hdl.handle.net/10722/316132
ISSN
2023 Impact Factor: 2.2
2023 SCImago Journal Rankings: 0.620
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorCasteleijn, Niek F.-
dc.contributor.authorMesschendorp, A. Lianne-
dc.contributor.authorBae, Kyong T.-
dc.contributor.authorHigashihara, Eiji-
dc.contributor.authorKappert, Peter-
dc.contributor.authorTorres, Vicente-
dc.contributor.authorMeijer, Esther-
dc.contributor.authorLeliveld, Anna M.-
dc.date.accessioned2022-08-24T15:49:21Z-
dc.date.available2022-08-24T15:49:21Z-
dc.date.issued2017-
dc.identifier.citationClinical and Experimental Nephrology, 2017, v. 21, n. 3, p. 375-382-
dc.identifier.issn1342-1751-
dc.identifier.urihttp://hdl.handle.net/10722/316132-
dc.description.abstractBackground: 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.-
dc.languageeng-
dc.relation.ispartofClinical and Experimental Nephrology-
dc.subjectAutosomal dominant polycystic kidney disease-
dc.subjectPolyuria-
dc.subjectTolvaptan-
dc.subjectUreter-
dc.titlePolyuria due to vasopressin V2 receptor antagonism is not associated with increased ureter diameter in ADPKD patients-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s10157-016-1297-1-
dc.identifier.pmid27339446-
dc.identifier.scopuseid_2-s2.0-84976336966-
dc.identifier.volume21-
dc.identifier.issue3-
dc.identifier.spage375-
dc.identifier.epage382-
dc.identifier.eissn1437-7799-
dc.identifier.isiWOS:000403422600003-

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