Evidence map›Paper›PMID 28348063›Full record

ArticleJournal of the American Society of Nephrology : JASN2017

Long-Term Endothelin-A Receptor Antagonism Provides Robust Renal Protection in Humanized Sickle Cell Disease Mice.

Malgorzata Kasztan, Brandon M Fox, Joshua S Speed, Carmen De Miguel, Eman Y Gohar, Tim M Townes, Abdullah Kutlar, Jennifer S Pollock, David M Pollock

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

51 citing papers in PubMed, 67 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Impact of renal iron overload on sickle cell nephropathy in a humanized mouse model.American journal of physiology. Renal physiology · 2026
    Article
  4. Review
  5. Urinary megalin expression in children with sickle cell nephropathy.Pediatric nephrology (Berlin, Germany) · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Endothelin-1 signaling in the kidney: recent advances and remaining gaps.American journal of physiology. Renal physiology · 2025
    Review
  14. Article
  15. Review
  16. 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
  17. Article
  18. Review
  19. Endothelin System in Hypertension and Chronic Kidney Disease.Hypertension (Dallas, Tex. : 1979) · 2024
    Review
  20. Sickle Cell Disease and CKD: An Update.American journal of nephrology · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Malgorzata KasztanCardio-Renal Physiology and Medicine, Department of Medicine, and.
Brandon M FoxCardio-Renal Physiology and Medicine, Department of Medicine, and.
Joshua S SpeedCardio-Renal Physiology and Medicine, Department of Medicine, and.
Carmen De MiguelCardio-Renal Physiology and Medicine, Department of Medicine, and.
Eman Y GoharCardio-Renal Physiology and Medicine, Department of Medicine, and.
Tim M TownesDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, Alabama; and.
Abdullah KutlarDivision of Hematology and Oncology, and.
Jennifer S PollockCardio-Renal Physiology and Medicine, Department of Medicine, and.
David M PollockCardio-Renal Physiology and Medicine, Department of Medicine, and dpollock@uab.edu.
Metabolism and Renal Physiology · FRAugusta University · USPalmetto Hematology Oncology · USUniversity of Alabama at Birmingham · US

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
The Role of Endothelin-1 in Sickle Cell DiseaseU01HL117684 · NHLBI · AUGUSTA UNIVERSITY · PI KUTLAR, ABDULLAH, MEILER, STEFFEN · 2013 to 2017
$8.1M
TRAINING IN CELLULAR PHYSIOLOGY MEMBRANE TRANSPORTT32DK007545 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GUTIERREZ, ORLANDO M · 1987 to 2023
$4.5M
Endothelin - Mechanisms in Hypertension and ObesityK99HL127178 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SPEED, JOSHUA S · 2016 to 2017
$308k
Novel Mechanisms of Decreased NO Bioavailability in Sickle Cell NephropathyF30DK107194 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FOX, BRANDON M · 2015 to 2018
$153k
NHLBI NIH HHS K99 HL127178NHLBI NIH HHS U01 HL117684NIDDK NIH HHS F30 DK107194NIDDK NIH HHS P30 DK079337NIDDK NIH HHS T32 DK007545
6 · The paper itself

Abstract

Sickle cell disease (SCD)-associated nephropathy is a major source of morbidity and mortality in patients because of the lack of efficacious treatments targeting renal manifestations of the disease. Here, we describe a long-term treatment strategy with the selective endothelin-A receptor (ET

Indexed as

Anemia, Sickle CellAnimalsDisease Models, AnimalEndothelin A Receptor AntagonistsFemaleHumansKidney DiseasesMaleMicePhenylpropionatesPyridazinesTime FactorsambrisentanEndothelin A Receptor AntagonistsPhenylpropionatesPyridazinesendothelinglomerular filtration barrierproteinuriarenal injurysickle nephropathy

Identifiers

PMID28348063
PMCPMC5533228
OpenAlexW2597810023

What Socratic 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 Socratic graph.