Evidence map›Paper›PMID 42648283›Full record

ArticleScience progress

Association of semaglutide use with kidney outcomes in adults with ADPKD: A propensity score-matched real-world study.

To-Pang Chen, Shang-Feng Tsai

Abstract read
In one paragraph

Article in Science progress. 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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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

To-Pang ChenDivision of Endocrinology and Metabolism, Show Chwan Memorial Hospital, Changhua, Taiwan.
Shang-Feng TsaiDivision of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.ORCID 0000-0002-6119-0587

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveAutosomal dominant polycystic kidney disease (ADPKD) is a progressive hereditary kidney disorder with limited treatment options. Although semaglutide has demonstrated kidney-protective effects in other populations, its renal effects in ADPKD remain unknown.MethodsWe conducted a retrospective propensity score-matched cohort study using the TriNetX Research Network. Adults with ADPKD between 2000 and 2024 were identified. Patients receiving sodium-glucose cotransporter-2 inhibitors, tolvaptan, or other glucagon-like peptide-1 receptor agonists were excluded. Semaglutide users were matched 1:1 with non-users. Outcomes included creatinine-based estimated glomerular filtration rate (eGFR), stage 5 chronic kidney disease (CKD), end-stage kidney disease (ESKD), body mass index (BMI), acute kidney injury (AKI), urinary tract infection (UTI), volume depletion, and all-cause mortality.ResultsAmong 45,613 adults with ADPKD, 323 semaglutide users and 31,300 non-users met the eligibility criteria; 320 matched pairs were analyzed. At follow-up, semaglutide users had a higher mean creatinine-based eGFR than non-users (57.52 ± 28.19 vs. 50.93 ± 33.80 mL/min/1.73 m

Indexed as

Glucagon-Like PeptidesKidneyPolycystic Kidney, Autosomal DominantAdultFemaleGlomerular Filtration RateHumansMaleMiddle AgedPropensity ScoreRetrospective StudiesSemaglutideGlucagon-Like PeptidesSemaglutideautosomal dominant polycystic kidney disease (ADPKD)renal functionsemaglutide

Identifiers

PMID42648283
PMCPMC13519180

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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 OpenQuestion graph.