Evidence map›Paper›PMID 37441472›Full record

ArticleKidney international reports2023

The Effects of Peroxisome Proliferator-Activated Receptor-Delta Modulator ASP1128 in Patients at Risk for Acute Kidney Injury Following Cardiac Surgery.

J W Olivier van Till, Hiroyuki Nojima, Chisato Kameoka, Chieri Hayashi, Taishi Sakatani, T Benton Washburn, Bruce A Molitoris, Andrew D Shaw, Daniel T Engelman, John A Kellum

Open access · goldAbstract read
In one paragraph

Article in Kidney international reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. New drugs for acute kidney injury.Journal of intensive medicine · 2025
    Review
  5. Article
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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

10 authors at 6 institutions in 2 countries.

J W Olivier van TillMitobridge Inc., Cambridge, Massachusetts, USA.
Hiroyuki NojimaAstellas Pharma Global Development Inc., Northbrook, Illinois, USA.
Chisato KameokaAstellas Pharma Inc, Development, Tokyo, Japan.
Chieri HayashiAstellas Pharma Global Development Inc., Northbrook, Illinois, USA.
Taishi SakataniAstellas Pharma Inc, Development, Tokyo, Japan.
T Benton WashburnDepartment of Thoracic Surgery, Heart Center, Huntsville, Alabama, USA.
Bruce A MolitorisDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Andrew D ShawDepartment of Intensive Care and Resuscitation, Cleveland Clinic, Cleveland, Ohio, USA.
Daniel T EngelmanHeart and Vascular Program, Baystate Health and University of Massachusetts Medical School-Baystate, Springfield, Massachusetts, USA.
John A KellumCenter for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Astellas Pharma (Japan) · JPAstellas Pharma (United States) · USCleveland Clinic · USIndiana University School of MedicineUniversity of Massachusetts Chan Medical School · USUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Peroxisome proliferator-activated receptor δ (PPARδ) plays a central role in modulating mitochondrial function in ischemia-reperfusion injury. The novel PPARδ modulator, ASP1128, was evaluated. Methods: A randomized, double-blind, placebo-controlled, biomarker assignment-driven, multicenter study was performed in adult patients at risk for acute kidney injury (AKI) following cardiac surgery, examining efficacy and safety of a 3-day, once-daily intravenous dose of 100 mg ASP1128 versus placebo (1:1). AKI risk was based on clinical characteristics and postoperative urinary biomarker (TIMP2)•(IGFBP7). The primary end point was the proportion of patients with AKI based on serum creatinine within 72 hours postsurgery (AKI-SCr72h). Secondary endpoints included the composite end point of major adverse kidney events (MAKE: death, renal replacement therapy, and/or ≥25% reduction of estimated glomerular filtration rate [eGFR]) at days 30 and 90). Results: A total of 150 patients were randomized and received study medication (81 placebo, 69 ASP1128). Rates of AKI-SCr72h were 21.0% and 24.6% in the placebo and ASP1128 arms, respectively ( Conclusion: ASP1128 was safe and well-tolerated in patients at risk for AKI following cardiac surgery, but it did not show efficacy in renal endpoints.

Indexed as

acute kidney injurycardiac surgical procedurescontrolled trialPPAR deltarandomizedreperfusion injury

Identifiers

PMID37441472
PMCPMC10334402
OpenAlexW4362722682

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.