Evidence map›Paper›PMID 24756971›Full record

ReviewJournal of nephrology2014

Osteoprotegerin and kidney disease.

Alejandra Montañez-Barragán, Isaias Gómez-Barrera, Maria D Sanchez-Niño, Alvaro C Ucero, Liliana González-Espinoza, Alberto Ortiz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of nephrology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

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

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Matrix Vesicles as a Therapeutic Target for Vascular Calcification.Frontiers in cell and developmental biology · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Urinary biomarkers in lupus nephritis.Journal of translational autoimmunity · 2020
    Review
  10. Review
  11. Evolving spectrum of diabetic nephropathy.World journal of diabetes · 2019
    Review
  12. Review
  13. Observational
  14. Article
  15. 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

6 authors.

Alejandra Montañez-BarragánEscuela Superior de Medicina del Instituto Politécnico Nacional, Ciudad de México, Mexico.
Isaias Gómez-BarreraEscuela Superior de Medicina del Instituto Politécnico Nacional, Ciudad de México, Mexico.
Maria D Sanchez-NiñoServicio de Nefrología, IdiPAZ, 28046, Madrid, Spain.
Alvaro C UceroIIS-Fundación Jiménez Díaz, Universidad Autónoma de Madrid and Fundación Renal Iñigo Álvarez de Toledo, 28040, Madrid, Spain.
Liliana González-EspinozaIIS-Fundación Jiménez Díaz, Universidad Autónoma de Madrid and Fundación Renal Iñigo Álvarez de Toledo, 28040, Madrid, Spain. liliana.gonzalez@fjd.es.
Alberto OrtizIIS-Fundación Jiménez Díaz, Universidad Autónoma de Madrid and Fundación Renal Iñigo Álvarez de Toledo, 28040, Madrid, Spain. aortiz@fjd.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular calcification in chronic kidney disease (CKD) patients is associated to increased mortality. Osteoprotegerin (OPG) is a soluble tumor necrosis factor (TNF) superfamily receptor that inhibits the actions of the cytokines receptor activator of nuclear factor kappa-B ligand (RANKL) and TNF-related apoptosis-inducing ligand (TRAIL) by preventing their binding to signaling receptors in the cell membrane. OPG-deficient mice display vascular calcification while OPG prevented calcification of cultured vascular smooth muscle cells and protected kidney cells from TRAIL-induced death. OPG may be a biomarker in patients with kidney disease. Circulating OPG is increased in predialysis, dialysis and transplant CKD patients and may predict vascular calcification progression and patient survival. By contrast, circulating OPG is decreased in nephrotic syndrome. In addition, free and exosome-bound urinary OPG is increased in human kidney disease. Increased urinary OPG has been associated with lupus nephritis activity. Despite the association of high OPG levels with disease, experimental functional information available suggests that OPG might be protective in kidney disease and in vascular injury in the context of uremia. Thus, tissue injury results in increased OPG, while OPG may protect from tissue injury. Recombinant OPG was safe in phase I randomized controlled trials. Further research is needed to fully define the therapeutic and biomarker potential of OPG in patients with kidney disease.

Indexed as

Signal TransductionAnimalsHumansKidney DiseasesMuscle, Smooth, VascularOsteoprotegerinRecombinant ProteinsTNF-Related Apoptosis-Inducing LigandVascular CalcificationOsteoprotegerinRecombinant ProteinsTNF-Related Apoptosis-Inducing LigandExosomeKidneyMortalityOsteoprotegerinTRAILVascular calcification

Identifiers

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.