Evidence map›Paper›PMID 31411074›Full record

ArticleAmerican journal of physiology. Renal physiology2019

Long-term outcomes in mouse models of ischemia-reperfusion-induced acute kidney injury.

Lauren Scarfe, Anna Menshikh, Emily Newton, Yuantee Zhu, Rachel Delgado, Charlene Finney, Mark P de Caestecker

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. A Review of Experimental Models of Feline Kidney Disease.Journal of the American Association for Laboratory Animal Science : JAALAS · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Rodent models of AKI and AKI-CKD transition: an update in 2024.American journal of physiology. Renal physiology · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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

7 authors.

Lauren ScarfeDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0003-3012-5771
Anna MenshikhDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Emily NewtonDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Yuantee ZhuDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Rachel DelgadoDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Charlene FinneyDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Mark P de CaesteckerDivision of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Funding

UAB-UCSD O'Brien Core Center for Acute Kidney Injury ResearchP30DK079337 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AGARWAL, ANUPAM · 2008 to 2022
$18.3M
Mechanisms and therapeutic manipulation of retinoic acid signaling in Acute Kidney InjuryR01DK112688 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DE CAESTECKER, MARK P. · 2017 to 2020
$1.7M
NIDDK NIH HHS P30 DK079337NIDDK NIH HHS R01 DK112688
6 · The paper itself

Abstract

Severe acute kidney injury has a high mortality and is a risk factor for progressive chronic kidney disease. None of the potential therapies that have been identified in preclinical studies have successfully improved clinical outcomes. This failure is partly because animal models rarely reflect the complexity of human disease: most preclinical studies are short term and are commonly performed in healthy, young, male mice. Therapies that are effective in preclinical models that share common clinical features seen in patients with acute kidney injury, including genetic diversity, different sexes, and comorbidities, and evaluate long-term outcomes are more likely to predict success in the clinic. Here, we evaluated susceptibility to chronic kidney disease after ischemia-reperfusion injury with delayed nephrectomy by monitoring long-term functional and histological responses to injury. We defined conditions required to induce long-term postinjury renal dysfunction and fibrosis without increased mortality in a reproducible way and evaluate effect of mouse strains, sexes, and preexisting diabetes on these responses.

Indexed as

Acute Kidney InjuryAnimalsDiabetes Mellitus, ExperimentalDiabetic NephropathiesDisease Models, AnimalFemaleFibrosisKidney Function TestsMaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, Inbred DBANephrectomyReperfusion InjurySex Characteristicsacute kidney injurydiabetesglomerular filtration rateischemia-reperfusion injurymouse strains

Identifiers

PMID31411074
PMCPMC7132317

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.