Evidence map›Paper›PMID 31542779›Full record

ArticleAging2019

Fibroblast growth factor 23 expression in human calcified vascular tissues.

Javier Donate-Correa, Ernesto Martín-Núñez, Carolina Hernández-Carballo, Carla Ferri, Víctor G Tagua, Alejandro Delgado-Molinos, Ángel López-Castillo, Sergio Rodríguez-Ramos, Purificación Cerro-López, Victoria Castro López-Tarruella and 5 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  8. Article
  9. Article
  10. Article
  11. Review
  12. Role of Glycosylation in Vascular Calcification.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. Observational
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

15 authors at 3 institutions in 1 country.

Javier Donate-CorreaResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Ernesto Martín-NúñezResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Carolina Hernández-CarballoResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Carla FerriResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Víctor G TaguaResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Alejandro Delgado-MolinosVascular Surgery Service, UHNSC, Santa Cruz de Tenerife, Spain.
Ángel López-CastilloVascular Surgery Service, UHNSC, Santa Cruz de Tenerife, Spain.
Sergio Rodríguez-RamosTransplant Coordination, UHNSC, Santa Cruz de Tenerife, Spain.
Purificación Cerro-LópezTransplant Coordination, UHNSC, Santa Cruz de Tenerife, Spain.
Victoria Castro López-TarruellaPathology Service, UHNSC, Santa Cruz de Tenerife, Spain.
Raquel Felipe-GarcíaPathology Service, UHNSC, Santa Cruz de Tenerife, Spain.
Miguel A Arévalo-GomezHuman Anatomy and Histology Department, University of Salamanca, Salamanca, Spain.
Nayra Pérez-DelgadoClinical Analysis Service, UHNSC, Santa Cruz de Tenerife, Spain.
Carmen Mora-FernándezResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Juan F Navarro-GonzálezResearch Unit, University Hospital Nuestra Señora de Candelaria (UHNSC), Santa Cruz de Tenerife, Spain.
Hospital Universitario Nuestra Señora de Candelaria · ESUniversidad de La Laguna · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular calcification is a major risk for cardiovascular disease and implies the transformation of smooth muscle cells to an osteoblastic phenotype as a consequence of dysregulation of calcium and phosphate metabolism. Fibroblast growth factor (FGF) 23 is the most potent phosphate regulator. Observational studies suggest that high levels of FGF23 are related to cardiovascular morbidity and mortality. In this work, we determined the levels of both the intact and the carboxi-terminal fragments of circulating FGF23 in 133 patients with established cardiovascular disease, the expression of FGF23, its receptors 1 and 3, and its co-receptor Klotho in vascular fragments of aorta, carotid and femoral in 43 out of this group of patients, and in a control group of 20 organ donors. Patients with atherosclerosis and vascular calcification presented increased levels of FGF23 respect to the control group. Vascular immunoreactivity for FGF23 was also significantly increased in patients with vascular calcification as compared to patients without calcification and to controls. Finally, gene expression of

Indexed as

AgedAortaCarotid ArteriesFemaleFemoral ArteryFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseHumansKlotho ProteinsMaleMiddle AgedMuscle, Smooth, VascularMyocytes, Smooth MuscleVascular CalcificationFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseKlotho ProteinsFGF23KlothoVascular calcification

Identifiers

PMID31542779
PMCPMC6781973
OpenAlexW2974238420

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.