Evidence map›Paper›PMID 38808486›Full record

ReviewClinical science (London, England : 1979)2024

Mechanism of protective actions of sparsentan in the kidney: lessons from studies in models of chronic kidney disease.

Donald E Kohan, Patricia W Bedard, Celia Jenkinson, Bruce Hendry, Radko Komers

Abstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. The disordered structure of sparsentan: energy calculations for competing chain conformations.Acta crystallographica. Section C, Structural chemistry · 2025
    Article
  13. Late Allograft Loss and Contemporary Cardiorenal Metabolic Therapies.Journal of the American Society of Nephrology : JASN · 2025
    Review
  14. Selective endothelin A receptor antagonism in chronic kidney disease: improving clinical application.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. 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

5 authors.

Donald E KohanDivision of Nephrology, University of Utah Health, Salt Lake City, UT, U.S.A.
Patricia W BedardTravere Therapeutics, Inc., San Diego, CA, U.S.A.
Celia JenkinsonTravere Therapeutics, Inc., San Diego, CA, U.S.A.
Bruce HendryTravere Therapeutics, Inc., San Diego, CA, U.S.A.
Radko KomersTravere Therapeutics, Inc., San Diego, CA, U.S.A.ORCID 0009-0006-7814-5324

Funding

Travere Therapeutics, Inc.
6 · The paper itself

Abstract

Simultaneous inhibition of angiotensin II AT1 and endothelin ETA receptors has emerged as a promising approach for treatment of chronic progressive kidney disease. This therapeutic approach has been advanced by the introduction of sparsentan, the first dual AT1 and ETA receptor antagonist. Sparsentan is a single molecule with high affinity for both receptors. It is US Food and Drug Administration approved for immunoglobulin A nephropathy (IgAN) and is currently being developed as a treatment for rare kidney diseases, such as focal segmental glomerulosclerosis. Clinical studies have demonstrated the efficacy and safety of sparsentan in these conditions. In parallel with clinical development, studies have been conducted to elucidate the mechanisms of action of sparsentan and its position in the context of published evidence characterizing the nephroprotective effects of dual ETA and AT1 receptor inhibition. This review summarizes this evidence, documenting beneficial anti-inflammatory, antifibrotic, and hemodynamic actions of sparsentan in the kidney and protective actions in glomerular endothelial cells, mesangial cells, the tubulointerstitium, and podocytes, thus providing the rationale for the use of sparsentan as therapy for focal segmental glomerulosclerosis and IgAN and suggesting potential benefits in other renal diseases, such as Alport syndrome.

Indexed as

KidneyRenal Insufficiency, ChronicAngiotensin II Type 1 Receptor BlockersAnimalsDisease Models, AnimalEndothelin A Receptor AntagonistsHumansAngiotensin II Type 1 Receptor BlockersEndothelin A Receptor AntagonistsAngiotensin IIEndothelin-1Endothelin Type A receptorFSGSIgA nephropathySparsentan

Identifiers

PMID38808486
PMCPMC11139641

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Registered trials

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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.