Evidence map›Paper›PMID 30909513›Full record

ReviewToxins2019

FGF23, Biomarker or Target?

Cristian Rodelo-Haad, Rafael Santamaria, Juan R Muñoz-Castañeda, M Victoria Pendón-Ruiz de Mier, Alejandro Martin-Malo, Mariano Rodriguez

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Toxins, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05356325 (The Role of FGF23 on the Induction of Cardiovascular Damage in Anemia With an Without Chronic Kidney Disease), which is not on this map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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.

NCT05356325 recruitingnot on this mapstarted 2021, after this paper: background citation

The Role of FGF23 on the Induction of Cardiovascular Damage in Anemia With an Without Chronic Kidney Disease

Typeobservational_patient_registrySponsorMaimónides Biomedical Research Institute of CórdobaRan2021 to 2025Enrolled401ConditionsFibroblast Growth Factor 23, Anemia, CKD
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Cardiovascular Biomarkers in Nocturnal Hemodialysis and Their Association With Physical Performance.Hemodialysis international. International Symposium on Home Hemodialysis · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Non-Classical Effects of FGF23: Molecular and Clinical Features.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Review
  14. Fibroblast growth factor 23 as a biomarker of right ventricular dysfunction in pulmonary hypertension.Clinical research in cardiology : official journal of the German Cardiac Society · 2023
    Observational
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

6 authors at 1 institution in 1 country.

Cristian Rodelo-HaadNephrology Service, University Hospital Reina Sofia, 14005 Cordoba, Spain. crisroha@yahoo.com.
Rafael SantamariaNephrology Service, University Hospital Reina Sofia, 14005 Cordoba, Spain. rsantamariao@gmail.com.
Juan R Muñoz-CastañedaNephrology Service, University Hospital Reina Sofia, 14005 Cordoba, Spain. juanr.munoz.exts@juntadeandalucia.es.
M Victoria Pendón-Ruiz de MierNephrology Service, University Hospital Reina Sofia, 14005 Cordoba, Spain. z22perum@uco.com.
Alejandro Martin-MaloNephrology Service, University Hospital Reina Sofia, 14005 Cordoba, Spain. amartinma@senefro.org.
Mariano RodriguezNephrology Service, University Hospital Reina Sofia, 14005 Cordoba, Spain. marianorodriguezportillo@gmail.com.
Instituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factor 23 (FGF23) plays a key role in the complex network between the bones and other organs. Initially, it was thought that FGF23 exclusively regulated phosphate and vitamin D metabolism; however, recent research has demonstrated that an excess of FGF23 has other effects that may be detrimental in some cases. The understanding of the signaling pathways through which FGF23 acts in different organs is crucial to develop strategies aiming to prevent the negative effects associated with high FGF23 levels. FGF23 has been described to have effects on the heart, promoting left ventricular hypertrophy (LVH); the liver, leading to production of inflammatory cytokines; the bones, inhibiting mineralization; and the bone marrow, by reducing the production of erythropoietin (EPO). The identification of FGF23 receptors will play a remarkable role in future research since its selective blockade might reduce the adverse effects of FGF23. Patients with chronic kidney disease (CKD) have very high levels of FGF23 and may be the population suffering from the most adverse FGF23-related effects. The general population, as well as kidney transplant recipients, may also be affected by high FGF23. Whether the association between FGF23 and clinical events is causal or casual remains controversial. The hypothesis that FGF23 could be considered a therapeutic target is gaining relevance and may become a promising field of investigation in the future.

Indexed as

AnimalsBiomarkersFibroblast Growth Factor-23Fibroblast Growth FactorsHumansHyperparathyroidism, SecondaryBiomarkersFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth Factorscalciumchronic kidney diseasedialysisfibroblast growth factor 23 (FGF23), fibroblast growth factor receptor (FGFR), Klothoparathyroid hormonephosphate

Identifiers

PMID30909513
PMCPMC6468608
OpenAlexW2933433997

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.