Evidence map›Paper›PMID 42347886›Full record

ArticleClinical and experimental nephrology2026

The effect of tolvaptan on total kidney volume and inflammatory markers in autosomal dominant polycystic kidney disease.

Merve Oruc, Mehmet Burak Ercin, Ahmet Oruc, Kultigin Turkmen, Ismail Baloglu

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Article in Clinical and experimental nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Merve OrucDepartment of Nephrology, Meram School of Medicine, Necmettin Erbakan University, Konya, Turkey. merveboztepe@hotmail.com.ORCID http://orcid.org/0009-0004-4973-8804
Mehmet Burak ErcinDepartment of Nephrology, Meram School of Medicine, Necmettin Erbakan University, Konya, Turkey.
Ahmet OrucDepartment of Medical Oncology, Meram School of Medicine, Necmettin Erbakan University, Konya, Turkey.
Kultigin TurkmenDepartment of Nephrology, Meram School of Medicine, Necmettin Erbakan University, Konya, Turkey.
Ismail BalogluDepartment of Nephrology, Meram School of Medicine, Necmettin Erbakan University, Konya, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive cyst growth, kidney enlargement, and decline in renal function. Increasing evidence suggests that inflammatory processes may contribute to disease progression. This study aimed to evaluate the association between tolvaptan use, systemic inflammatory markers, and total kidney volume (TKV) progression in patients with ADPKD.

methodsThis retrospective study included 67 patients with ADPKD, including 40 receiving tolvaptan and 27 untreated controls. Neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), estimated glomerular filtration rate (eGFR), and TKV were evaluated at baseline and after 24 months. Longitudinal changes were assessed using Wilcoxon signed-rank tests and linear mixed-effects models.

resultsPatients receiving tolvaptan were younger and had higher baseline TKV values than untreated patients. During follow-up, NLR, PLR, and SII decreased in the tolvaptan group, whereas these markers increased in untreated patients. eGFR declined in both groups but appeared less pronounced in patients receiving tolvaptan. TKV increased in both groups; however, the percentage increase in TKV was lower among patients receiving tolvaptan. Significant time × treatment interactions were observed for NLR, PLR, SII, and TKV. In the non-tolvaptan group, NLR at 24 months showed a significant positive association with TKV.

conclusionsTolvaptan use was associated with differences in longitudinal changes in systemic inflammatory markers and kidney volume progression in ADPKD. Further prospective studies are needed to clarify the clinical relevance of these associations.

Indexed as

Autosomal dominant polycystic kidney disease (ADPKD)InflammationNeutrophil-to-lymphocyte ratioSystemic immune-inflammation indexTolvaptanTotal kidney volume

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.