Evidence map›Paper›PMID 41041531›Full record

ArticleResearch square2025

An Observational Study of SGLT2 Inhibitors and Their Use in Autosomal Dominant Tubulointerstitial Kidney Disease.

Kendrah O Kidd, Adrienne H Williams, Elhussein A E Elhassan, Abbigail Taylor, Lauren Martin, Alice Kim, Michael V Rocco, Michael J Choi, Martina Zivna, Stanislav Kmoch and 2 more

Abstract readPreprint
In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

12 authors.

Kendrah O KiddWake Forest School University of Medicine.
Adrienne H WilliamsWake Forest School University of Medicine.
Elhussein A E ElhassanBeaumont Hospital.
Abbigail TaylorWake Forest School University of Medicine.
Lauren MartinWake Forest School University of Medicine.
Alice KimWake Forest School University of Medicine.
Michael V RoccoWake Forest School University of Medicine.
Michael J ChoiMedStar Georgetown University Hospital.
Martina ZivnaCharles University.
Stanislav KmochCharles University.
Peter J ConlonBeaumont Hospital.
Anthony J BleyerWake Forest School University of Medicine.

Funding

CTSA UM1 Program at Wake ForestUM1TR004929 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jamy D Ard, KRISTIE L FOLEY · 2024 to 2026
$11.9M
Chronic Kidney Disease (CKD) Biomarkers Consortium Data Coordinating CenterU01DK103225 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI SCHRAUBEN, SARAH JEANNE · 2014 to 2020
$5.5M
Genetic Variation in Age of Onset of Kidney Failure in Uromodulin Kidney DiseaseR21DK106584 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BLEYER, ANTHONY J · 2015 to 2016
$426k
NCATS NIH HHS UM1 TR004929NIDDK NIH HHS R21 DK106584NIDDK NIH HHS U01 DK103225
6 · The paper itself

Abstract

Background: There are no specific treatments available for autosomal dominant tubulointerstitial kidney disease (ADTKD). As SGLT2 inhibitors have proven effective in other forms of CKD, we performed an observational study to determine their safety and effect on kidney function in ADTKD. Methods: We obtained clinical and laboratory data before and after starting an SGLT2 inhibitor on 27 individuals with ADTKD. We created a propensity-matched cohort from a Wake Forest prospective ADTKD observational study. Results: Of the 27 individuals, 12 stopped medication prior to one year due to concerns about the (anticipated) acute rise in serum creatinine. There were no adverse effects. The slope of eGFR after SGLT 2 inhibitor initiation was - 2.61 ± 2.58 ml/min/1.73m Conclusions: SGLT2 inhibitors were well tolerated in ADTKD patients. There was neither a rise in hemoglobin levels nor a fall in plasma or urinary KIM-1 levels, suggesting that these agents may not be beneficial in ADTKD.

Indexed as

ADTKDAutosomal Dominant Tubulointerstitial Kidney DiseaseMUC1SGLT2 inhibitorsSodium-glucose cotransporter 2 inhibitorsUMOD

Identifiers

PMID41041531
PMCPMC12486101

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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.