Evidence map›Paper›PMID 22290531›Full record

ReviewAmerican journal of hematology2012

Targeting the hepcidin-ferroportin axis to develop new treatment strategies for anemia of chronic disease and anemia of inflammation.

Chia Chi Sun, Valentina Vaja, Jodie L Babitt, Herbert Y Lin

Registry-linked trialAbstract readReview
In one paragraph

Review in American journal of hematology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02876211 (Benefits of the Paricalcitol), which is not on this map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
11.2field-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.

NCT02876211 phase4terminatednot on this mapstarted 2014, after this paper: background citation

Benefits of the Paricalcitol (Selective Vitamin D Receptor Activator) on Anemia of Inflammation in Dialysis Patients Under Erythropoiesis-stimulating Agents Treatment.

TypeinterventionalSponsorHospital Son EspasesRan2014 to 2024Enrolled19ConditionsAnemiaArmsParicalcitol, Epoetin beta, Placebo
3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 183 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Review
  8. Article
  9. Article
  10. Review
  11. Inflammation alters iron distribution in bone and spleen in mice.Metallomics : integrated biometal science · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Article

19 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

4 authors at 1 institution in 2 countries.

Chia Chi SunProgram in Membrane Biology, Division of Nephrology, Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Valentina Vaja
Jodie L Babitt
Herbert Y Lin
Massachusetts General Hospital · US

Funding

Regulation of Iron Homeostasis by BMP SignalingR01DK087727 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BABITT, JODIE L · 2010 to 2024
$6.0M
Regulation of BMP Signaling in the KidneyR01DK069533 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LIN, HERBERT Y · 2005 to 2014
$3.3M
Mechanisms of Action of HemojuvelinR01DK071837 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LIN, HERBERT Y · 2005 to 2014
$3.3M
BMP Signaling and Iron MetabolismK08DK075846 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BABITT, JODIE L · 2006 to 2010
$736k
NIDDK NIH HHS K08 DK075846NIDDK NIH HHS R01 DK069533NIDDK NIH HHS R01 DK071837NIDDK NIH HHS R01 DK087727
6 · The paper itself

Abstract

Anemia of chronic disease (ACD) or anemia of inflammation is prevalent in patients with chronic infection, autoimmune disease, cancer, and chronic kidney disease. ACD is associated with poor prognosis and lower quality of life. Management of ACD using intravenous iron and erythropoiesis stimulating agents are ineffective for some patients and are not without adverse effects, driving the need for new alternative therapies. Recent advances in our understanding of the molecular mechanisms of iron regulation reveal that increased hepcidin, the iron regulatory hormone, is a key factor in the development of ACD. In this review, we will summarize the role of hepcidin in iron homeostasis, its contribution to the pathophysiology of ACD, and novel strategies that modulate hepcidin and its target ferroportin for the treatment of ACD.

Indexed as

Molecular Targeted TherapyTherapies, InvestigationalAnemiaAnimalsAntibodies, MonoclonalAntimicrobial Cationic PeptidesBone Morphogenetic Protein 6Cation Transport ProteinsChronic DiseaseClinical Trials as TopicDrug Evaluation, PreclinicalFerroportinGPI-Linked ProteinsHemochromatosis ProteinHepcidinsHomeostasisAntibodies, MonoclonalAntimicrobial Cationic PeptidesBMP6 protein, humanBone Morphogenetic Protein 6Cation Transport ProteinsFerroportinGPI-Linked ProteinsHAMP protein, humanHamp protein, mouseHemochromatosis ProteinHepcidinsHJV protein, humanIL6 protein, humanInterleukin-6Interleukin-6 InhibitorsIronLDN 193189PyrazolesPyrimidinesRNA, Small InterferingSmad ProteinsSTAT3 protein, humanSTAT3 Transcription FactorVitamin D

Identifiers

PMID22290531
PMCPMC3653431
OpenAlexW2012068458

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.