Evidence map›Paper›PMID 42584781›Full record

ReviewInternational urology and nephrology2026

SGLT2 inhibitors in autosomal dominant polycystic kidney disease: rationale, evidence gaps, and ongoing clinical trials.

Leonardo Spatola, Rosario Maccarrone, Gaspare Oddo, Salvatore Granata, Matthias Zeiler, Antonio Granata

Abstract readReview
PubMed Publisher
In one paragraph

Review in International urology and nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Leonardo SpatolaNephrology and Dialysis Unit, "Sant'Antonio" Hospital, ASPTrapani, Trapani, Italy. leonardospatola9@gmail.com.ORCID http://orcid.org/0000-0002-8883-4776
Rosario MaccarroneNephrology and Dialysis Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.
Gaspare OddoNephrology and Dialysis Unit, "Sant'Antonio" Hospital, ASPTrapani, Trapani, Italy.
Salvatore GranataDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Matthias ZeilerNephrology and Dialysis Unit, Department of Internal Medicine, "C. e G. Mazzoni" Hospital, Ascoli Piceno, Italy.
Antonio GranataNephrology and Dialysis Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) remains the leading inherited cause of chronic kidney disease (CKD), with specific management largely relying on the approval of the selective vasopressin V2 receptor antagonist, tolvaptan, in recent years. However, the administration of tolvaptan is associated with several potential risks, including aquaretic side effects, dehydration, and acute kidney and liver injuries, highlighting the need for careful consideration of the optimal dosage. In this context, there has been increasing interest in the use of SGLT2 inhibitors for both diabetic and non-diabetic chronic kidney disease given their cardio- and nephroprotective roles, as well as their potential to delay progression to end-stage renal disease. Nevertheless, the exclusion of ADPKD patients from randomized controlled trials (RCTs) involving CKD patients receiving SGLT2 inhibitors-due to concerns about eGFR decline, cyst growth, and increased total kidney volume-has created a gap in evidence and uncertainty. Available observational studies indicate both beneficial and adverse effects, while ongoing trials aim to provide more definitive evidence on the safety and efficacy of SGLT2 inhibitors in this inherited CKD population. Therefore, this review aims to focus on the current treatment options for ADPKD patients and the promising role of SGLT2 inhibitors, drawing on the available literature and ongoing RCTs.

Indexed as

ADPKDCKDESRDSGLT2 inhibitorsTolvaptan

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.