Evidence map›Paper›PMID 20421884›Full record

ReviewNature reviews. Nephrology2010

Nuclear hormone receptors in diabetic nephropathy.

Xiaoxin X Wang, Tao Jiang, Moshe Levi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Nephrology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  14. Review
  15. Anti-fibrosis therapy and diabetic nephropathy.Current diabetes reports · 2012
    Review
  16. Article
  17. Kidney aging--inevitable or preventable?Nature reviews. Nephrology · 2011
    Review
  18. Pathophysiology of the diabetic kidney.Comprehensive Physiology · 2011
    Review
  19. The proximal tubule in the pathophysiology of the diabetic kidney.American journal of physiology. Regulatory, integrative and comparative physiology · 2011
    Review
  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.

Xiaoxin X WangDepartment of Medicine, Division of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO 80045, USA.
Tao Jiang
Moshe Levi
University of Colorado Denver · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes is the leading cause of end-stage renal disease in developed countries. In spite of glucose and blood pressure control, for example by use of angiotensin II receptor blockers, diabetic nephropathy still develops and progresses in affected patients and the development of additional protective therapeutic interventions is, therefore, required. Nuclear hormone receptors are transcription factors that regulate carbohydrate metabolism, lipid metabolism, the immune response, and inflammation. These receptors also modulate the development of fibrosis. As a result of their diverse biological effects, nuclear hormone receptors have become major pharmaceutical targets for the treatment of a host of diseases. The increasing prevalence of diabetic nephropathy has led intense investigation into the role that nuclear hormone receptors may have in slowing or preventing the progression of renal disease. This role of nuclear hormone receptors would be associated with improvements in metabolism, the immune response, and inflammation. Eight nuclear receptors have shown a renoprotective effect in the context of diabetic nephropathy. This Review discusses the evidence regarding the beneficial effects of the activation of these receptors in preventing the progression of diabetic nephropathy and describes how the discovery and development of compounds that modulate the activity of nuclear hormone receptors may provide potential additional therapeutic approaches in the management of diabetic nephropathy.

Indexed as

AnimalsClinical Trials as TopicDiabetic NephropathiesDisease ProgressionHeat-Shock ProteinsHepatocyte Nuclear Factor 4HumansHypolipidemic AgentsIsoxazolesLiver X ReceptorsOrphan Nuclear ReceptorsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaReceptor, Farnesoid X-ActivatedReceptors, CalcitriolReceptors, Cytoplasmic and NuclearReceptors, EstrogenGW 4064Heat-Shock ProteinsHepatocyte Nuclear Factor 4Hypolipidemic AgentsIsoxazolesLiver X ReceptorsOrphan Nuclear ReceptorsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanReceptor, Farnesoid X-ActivatedReceptors, CalcitriolReceptors, Cytoplasmic and NuclearReceptors, EstrogenThiazolidinedionesTranscription FactorsVitamin D

Identifiers

PMID20421884
OpenAlexW2034616694

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.