Evidence map›Paper›PMID 24552640›Full record

ReviewTrends in pharmacological sciences2014

The pathophysiology and pharmacology of hepcidin.

Piotr Ruchala, Elizabeta Nemeth

2 registry-linked trialsAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
10.3field-weighted citation impact, top 1% 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.

NCT03001687 naunknown statusnot on this mapstarted 2017, after this paper: background citation

Impact of Vitamin D Enteral Supplementation on Hepcidin Serum Levels and Transfusion Requirements in Surgical and Critically Ill Patients

TypeinterventionalSponsorIuliu Hatieganu University of Medicine and PharmacyRan2017 to 2017Enrolled40ConditionsSystemic Inflammatory Response Syndrome, Sepsis, Surgical InjuriesArmsenteral supplementation with vitamin D, blood collection 3mL
NCT03145896 naunknown statusnot on this mapstarted 2017, after this paper: background citation

The Correlation Between Anemia of Chronic Diseases, Hepcidin and Vitamin D in IBD Patients

TypeinterventionalSponsorTel-Aviv Sourasky Medical CenterRan2017 to 2018Enrolled40ConditionsIBDArmsvitamin D
3 · Its place in the literature

Who cites it

65 citing papers in PubMed, 138 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Targeting macro- and micro-nutrient regulation of HNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Managing the Dual Nature of Iron to Preserve Health.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Hepatocrinology.Medical sciences (Basel, Switzerland) · 2021
    Review

5 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Piotr RuchalaDepartment of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Elizabeta NemethDepartment of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA, USA. Electronic address: enemeth@mednet.ucla.edu.
University of California, Los Angeles · US

Funding

Hepcidin therapy for iron overload and hematologic disordersR01DK090554 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI RIVELLA, STEFANO · 2010 to 2021
$5.2M
The Hepcidin-Ferroportin Axis in Anemia of Inflammation: Mechanisms and TargetsR01DK082717 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NEMETH, ELIZABETA · 2008 to 2012
$1.6M
NIDDK NIH HHS R01 DK082717NIDDK NIH HHS R01 DK090554
6 · The paper itself

Abstract

Inappropriate production of the iron-regulatory hormone hepcidin contributes to the pathogenesis of common iron disorders. Absolute or relative deficiency of hepcidin causes iron overload in hereditary hemochromatosis and iron-loading anemias. Elevated hepcidin causes iron restriction in inflammatory conditions including autoimmune disease, critical illness, some cancers, and chronic kidney disease. Multiple agents targeting hepcidin and its regulators are under development as novel therapeutics for iron disorders. This review summarizes hepcidin biology and discusses the current landscape for hepcidin-targeting therapeutic strategies.

Indexed as

AnemiaAnimalsHepcidinsHumansIronIron OverloadHepcidinsIronanemiaferroportiniron disordersiron overload

Identifiers

PMID24552640
PMCPMC3978192
OpenAlexW2087535882

What OpenQuestion holds

Textmetadata
LicenceTDM
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.