Evidence map›Paper›PMID 22262480›Full record

ArticleAmerican journal of physiology. Renal physiology2012

Preischemic targeting of HIF prolyl hydroxylation inhibits fibrosis associated with acute kidney injury.

Pinelopi P Kapitsinou, Jonathan Jaffe, Mark Michael, Christina E Swan, Kevin J Duffy, Connie L Erickson-Miller, Volker H Haase

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05010460 (Roxadustat Reduces the Incidence of Acute Kidney Injury After Coronary Artery Bypass Grafting), which is not on this map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.0field-weighted citation impact, top 9% 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.

NCT05010460 phase2terminatednot on this mapstarted 2021, after this paper: background citation

Roxadustat Reduces the Incidence of Acute Kidney Injury After Coronary Artery Bypass Grafting: a Multicenter, Randomized, Double-blind, Placebo-controlled Study

TypeinterventionalSponsorPeking Union Medical College HospitalRan2021 to 2025Enrolled98ConditionsCoronary Artery BypassArmsRoxadustat, Placebo
3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 115 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Personalized Antifibrotic Therapy in CKD Progression.Journal of personalized medicine · 2024
    Review
  5. Hypoxia-inducible factor prolyl hydroxylase inhibitors for anaemia in chronic kidney disease: a clinical practice document by the European Renal Best Practice board of the European Renal Association.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. From AKI to CKD: Maladaptive Repair and the Underlying Mechanisms.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Roxadustat: Not just for anemia.Frontiers in pharmacology · 2022
    Review
  19. Review
  20. Review

3 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Pinelopi P KapitsinouDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Jonathan Jaffe
Mark Michael
Christina E Swan
Kevin J Duffy
Connie L Erickson-Miller
Volker H Haase
Vanderbilt University · USGlaxoSmithKline (United States) · US

Funding

Molecular Mechanisms of Renal InjuryR01DK081646 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HAASE, VOLKER HANS · 2008 to 2021
$4.3M
Regulation of Renal Function by PGE2 and PGF2a ReceptorsR01DK037097 · NIDDK · VANDERBILT UNIVERSITY · PI BREYER, RICHARD M. · 1986 to 2011
$3.9M
NIDDK NIH HHS R01 DK037097NIDDK NIH HHS R01 DK081646NIDDK NIH HHS R01-DK081646NIDDK NIH HHS R01-DK37097
6 · The paper itself

Abstract

Acute kidney injury (AKI) due to ischemia is an important contributor to the progression of chronic kidney disease (CKD). Key mediators of cellular adaptation to hypoxia are oxygen-sensitive hypoxia-inducible factors (HIF), which are regulated by prolyl-4-hydroxylase domain (PHD)-containing dioxygenases. While activation of HIF protects from ischemic cell death, HIF has been shown to promote fibrosis in experimental models of CKD. The impact of HIF activation on AKI-induced fibrosis has not been defined. Here, we investigated the role of pharmacologic HIF activation in AKI-associated fibrosis and inflammation. We found that pharmacologic inhibition of HIF prolyl hydroxylation before AKI ameliorated fibrosis and prevented anemia, while inhibition of HIF prolyl hydroxylation in the early recovery phase of AKI did not affect short- or long-term clinical outcome. Therefore, preischemic targeting of the PHD/HIF pathway represents an effective therapeutic strategy for the prevention of CKD resulting from AKI, and it warrants further investigation in clinical trials.

Indexed as

Acute Kidney InjuryAnimalsDisease Models, AnimalEnzyme InhibitorsFibrosisHydroxylationHypoxia-Inducible Factor 1KidneyMaleMiceMice, Inbred C57BLProcollagen-Proline DioxygenaseTranscription FactorsXylazineEnzyme InhibitorsHIF-2 protein, mouseHypoxia-Inducible Factor 1Procollagen-Proline DioxygenaseTranscription FactorsXylazine

Identifiers

PMID22262480
PMCPMC3362175
OpenAlexW2090646335

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.