Evidence map›Paper›PMID 23228194›Full record

ReviewBritish journal of clinical pharmacology2013

Endothelin antagonists for diabetic and non-diabetic chronic kidney disease.

Donald E Kohan, David M Pollock

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of clinical pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Predictors of congestive heart failure after treatment with an endothelin receptor antagonist.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Trial
  8. Observational
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Pathomechanisms of Diabetic Kidney Disease.Journal of clinical medicine · 2023
    Review
  16. Article
  17. Endothelin Receptor Antagonists in Kidney Disease.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Review
  20. Review
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

2 authors at 2 institutions in 1 country.

Donald E KohanDivision of Nephrology, University of Utah Health Sciences Center, Salt Lake City, UT.
David M Pollock
Augusta University · USUniversity of Utah · US

Funding

Renal endothelin receptor-specific function in angiotensin ll-dependent hypertensP01HL095499 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SULLIVAN, JENNIFER C · 2010 to 2014
$11.1M
NHLBI NIH HHS P01HL095499
6 · The paper itself

Abstract

Numerous pre-clinical studies have implicated endothelin-1 in the pathogenesis of diabetic and non-diabetic chronic kidney disease (CKD). Renal endothelin-1 production is almost universally increased in kidney disease. The pathologic effects of endothelin-1, including vasoconstriction, proteinuria, inflammation, cellular injury and fibrosis, are likely mediated by the endothelin A (ETA) receptor. ETA antagonism alone, and/or combined ETA/B blockade, reduces CKD progression. Based on the strong pre-clinical data, several clinical trials using ETA antagonists were conducted. Small trials involving acute intravenous endothelin receptor blockade suggest that ETA, but not ETB, blockade exerts protective renal and vascular effects in CKD patients. A large phase 3 trial (ASCEND) examined the effects of avosentan, an endothelin receptor antagonist, on renal disease progression in diabetic nephropathy. Proteinuria was reduced after 3-6 months of treatment. However the study was terminated due to increased morbidity and mortality associated with avosentan-induced fluid retention. Several phase 2 trials using avosentan at lower doses than in ASCEND, atrasentan or sitaxsentan (the latter two being highly ETA-selective) showed reductions in proteinuria on top of renin-angiotensin system blockade. Infrequent and clinically insignificant fluid retention was observed at the most effective doses. Additional trials using ETA blockers are ongoing or being planned in patients with diabetic nephropathy or focal segmental glomerulosclerosis. Moving forward, such studies must be conducted with careful patient selection and attention to dosing in order to minimize adverse side effects. Nonetheless, there is cause for optimism that this class of agents will ultimately prove to be effective for the treatment of CKD.

Indexed as

AnimalsClinical Trials as TopicDiabetic NephropathiesDose-Response Relationship, DrugEndothelin-1Endothelin A Receptor AntagonistsEndothelin B Receptor AntagonistsHumansIsoxazolesKidney Failure, ChronicPyridinesPyrimidinesRenal DialysisRenal Insufficiency, ChronicThiophenesTreatment OutcomeAvosentanEndothelin-1Endothelin A Receptor AntagonistsEndothelin B Receptor AntagonistsIsoxazolesPyridinesPyrimidinessitaxsentanThiophenesantagonistchronic kidney diseasediabetesendothelinreceptor

Identifiers

PMID23228194
PMCPMC3791980
OpenAlexW1539206659

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.