Evidence map›Paper›PMID 19144760›Full record

Trial reportJournal of the American Society of Nephrology : JASN2009

Avosentan reduces albumin excretion in diabetics with macroalbuminuria.

René R Wenzel, Thomas Littke, Susan Kuranoff, Christiane Jürgens, Heike Bruck, Eberhard Ritz, Thomas Philipp, Anna Mitchell, SPP301 (Avosentan) Endothelin Antagonist Evaluation in Diabetic Nephropathy Study Investigators

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Society of Nephrology : JASN, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 2 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

96 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  8. Predictors of congestive heart failure after treatment with an endothelin receptor antagonist.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Trial
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  10. Avosentan for overt diabetic nephropathy.Journal of the American Society of Nephrology : JASN · 2010
    Trial
  11. Article
  12. Review
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  14. Review
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  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
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36 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

René R WenzelDepartment of Internal Medicine, Cardiology-Nephrology-Cardiovascular Research, AO Krankenhaus Zell am See, Teaching Hospital of the Paracelsus University Salzburg (Austria), Zell am See, Austria. rrwenzel@me.com
Thomas Littke
Susan Kuranoff
Christiane Jürgens
Heike Bruck
Eberhard Ritz
Thomas Philipp
Anna Mitchell
SPP301 (Avosentan) Endothelin Antagonist Evaluation in Diabetic Nephropathy Study Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the first-line use of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs), there is still a large need to improve the prevention and progression of diabetic nephropathy and its associated cardiovascular events. Endothelin antagonists have shown anti-inflammatory, antifibrotic, and antiproteinuric effects in experimental studies. This study was a randomized, placebo-controlled, double-blind, parallel-design, dosage-range study of the effect of the endothelin-A antagonist avosentan (SPP301) on urinary albumin excretion rate (UAER) in patients with diabetic nephropathy. We randomly assigned 286 patients with diabetic nephropathy, macroalbuminuria (UAER 0.2 to 5.6 mg/min), and BP <180/110 mmHg to 12 wk of avosentan (5, 10, 25, and 50 mg) or placebo, in addition to standard ACEI/ARB therapy. Relative to baseline, all avosentan dosages decreased mean relative UAER (-16.3 to -29.9%) compared with placebo (35.5%). Median relative UAER decreased with all avosentan dosages (-28.7 to -44.8%) compared with placebo (12.1%). Creatinine clearance and BP were unchanged at 12 wk. The main adverse events were peripheral edema (12%), mainly with high (>/=25 mg) dosages of avosentan; significant increases in liver enzymes did not occur. Twenty-one (7.3%) patients experienced adverse events that led to withdrawal from study medication. In summary, the endothelin-A antagonist avosentan given in addition to standard ACEI/ARB treatment decreases UAER in patients with diabetic nephropathy and macroalbuminuria.

Indexed as

AgedAlbuminuriaAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersDiabetic NephropathiesDose-Response Relationship, DrugDouble-Blind MethodEndothelin A Receptor AntagonistsFemaleHumansHypoglycemic AgentsMaleMiddle AgedPyridinesPyrimidinesAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersAvosentanEndothelin A Receptor AntagonistsHypoglycemic AgentsPyridinesPyrimidines

Identifiers

PMID19144760
PMCPMC2653691

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.