Evidence map›Paper›PMID 38418382›Full record

ReviewPhysiological reports2024

NRF2 in kidney physiology and disease.

Corry D Bondi, Hannah L Hartman, Roderick J Tan

Open access · goldAbstract readReview
In one paragraph

Review in Physiological reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  10. Article
  11. Review
  12. METTL3-driven mFrontiers in immunology · 2026
    Article
  13. Review
  14. Review
  15. Advances in Parathyroid Hormone-based medicines.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Review
  16. Review
  17. NRF2 Dysregulation and Therapeutic Insights Across Chronic Kidney Diseases.International journal of molecular sciences · 2025
    Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Corry D BondiRenal-Electrolyte Division, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Hannah L HartmanRenal-Electrolyte Division, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Roderick J TanRenal-Electrolyte Division, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.ORCID 0000-0003-1012-1722
University of Pittsburgh · US

Funding

Single Nephron and MetabolomicsP30DK079307 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2008 to 2022
$13.4M
Tenancin-C as a major component of the fibrogenic nicheR01DK064005 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TAN, RODERICK JASON · 2003 to 2021
$5.1M
Resource Development CoreU54DK137329 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Thomas R Kleyman · 2023 to 2026
$4.8M
Renal and Epithelial Biology Training ProgramT32DK061296 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLEYMAN, THOMAS R · 2002 to 2022
$3.1M
Effect of Renal Nerves on Chronic Kidney DiseaseR01DK131991 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Roderick Jason Tan · 2022 to 2026
$2.6M
The Role of MCP-1 in Tubular-to-Glomerular Crosstalk in Proteinuric Kidney DiseaseK01DK124357 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BONDI, CORRY DOMINIC · 2021 to 2025
$740k
The Role of Nrf2 in Proteinuric Chronic Kidney DiseaseI01BX005680 · VA · VETERANS HEALTH ADMINISTRATION · PI TAN, RODERICK JASON · 2022 to 2025
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BLRD VA I01 BX005680NIDDK NIH HHS K01 DK124357NIDDK NIH HHS P30 DK079307NIDDK NIH HHS R01 DK064005NIDDK NIH HHS R01 DK131991NIDDK NIH HHS T32 DK061296NIDDK NIH HHS U54 DK137329
6 · The paper itself

Abstract

The role of NRF2 in kidney biology has received considerable interest over the past decade. NRF2 transcriptionally controls genes responsible for cellular protection against oxidative and electrophilic stress and has anti-inflammatory functions. NRF2 is expressed throughout the kidney and plays a role in salt and water handling. In disease, animal studies show that NRF2 protects against tubulointerstitial damage and reduces interstitial fibrosis and tubular atrophy, and may slow progression of polycystic kidney disease. However, the role of NRF2 in proteinuric glomerular diseases is controversial. Although the NRF2 inducer, bardoxolone methyl (CDDO-Me), increases glomerular filtration rate in humans, it has not been shown to slow disease progression in diabetic kidney disease and Alport syndrome. Furthermore, bardoxolone methyl was associated with negative effects on fluid retention, proteinuria, and blood pressure. Several animal studies replicate findings of worsened proteinuria and a more rapid progression of kidney disease, although considerable controversy exists. It is clear that further study is needed to better understand the effects of NRF2 in the kidney. This review summarizes the available data to clarify the promise and risks associated with targeting NRF2 activity in the kidney.

Indexed as

Diabetic NephropathiesNF-E2-Related Factor 2AnimalsHumansKidneyOleanolic AcidProteinuriabardoxolone methylNF-E2-Related Factor 2Oleanolic Acidbardoxolone methylchronic kidney diseaseelectrophilesoxidative stressproteinuria

Identifiers

PMID38418382
PMCPMC10901725
OpenAlexW4392291500

What OpenQuestion holds

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LicenceCC BY
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.