Evidence map›Paper›PMID 30737269›Full record

ArticleJournal of the American Society of Nephrology : JASN2019

Iron, Hepcidin, and Death in Human AKI.

David E Leaf, Mohan Rajapurkar, Suhas S Lele, Banibrata Mukhopadhyay, Emily A S Boerger, Finnian R Mc Causland, Michele F Eisenga, Karandeep Singh, Jodie L Babitt, John A Kellum and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 68 citations in OpenAlex.

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  9. Biomarkers as Beacons: Illuminating Sepsis-Associated Hepato-Renal Injury.International journal of molecular sciences · 2025
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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

13 authors at 7 institutions in 3 countries.

David E LeafDivision of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts; DELEAF@bwh.harvard.edu.
Mohan RajapurkarDepartment of Nephrology.
Suhas S LeleDepartment of Cardiology, and.
Banibrata MukhopadhyayDepartment of Biochemistry, Muljibhai Patel Urological Hospital, Gujarat, India.
Emily A S BoergerDivision of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Finnian R Mc CauslandDivision of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Michele F EisengaDepartment of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands; Departments of.
Karandeep SinghLearning Health Sciences and.
Jodie L BabittNephrology Division, Program in Membrane Biology, Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts.
John A KellumCenter for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Paul M PalevskyRenal Section, Veterans Affairs Pittsburgh Healthcare System, Pittsburgh, Pennsylvania.
Marta ChristovDepartment of Medicine, New York Medical College, Valhalla, New York.
Sushrut S WaikarDivision of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Brigham and Women's Hospital · USUniversity of Pittsburgh · USCenter for Systems Biology · USMuljibhai Patel Urological Hospital · INNew York Medical College · USUniversity Medical Center Groningen · NLUniversity of Michigan–Ann Arbor · US

Funding

UAB-UCSD O'Brien Core Center for Acute Kidney Injury ResearchP30DK079337 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AGARWAL, ANUPAM · 2008 to 2022
$18.3M
Regulation of Iron Homeostasis by BMP SignalingR01DK087727 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BABITT, JODIE L · 2010 to 2024
$6.0M
Urinary Biomarkers of Chronic Kidney Disease Pathology and ProgressionU01DK085660 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT, WAIKAR, SUSHRUT S. · 2009 to 2019
$5.3M
Biomarkers of Kidney PathologyR01DK093574 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI WAIKAR, SUSHRUT S. · 2012 to 2015
$2.4M
Biological Markers of Recovery for the KidneyR01DK070910 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KELLUM, JOHN A · 2006 to 2010
$1.8M
Cardiac Complications of Hemodynamic Instability during HemodialysisK23DK102511 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI MCCAUSLAND, FINNIAN R · 2015 to 2019
$964k
Dysregulated Mineral Metabolism and Acute Kidney InjuryK23DK106448 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI LEAF, DAVID EVAN · 2015 to 2019
$964k
Dissecting the Mechanisms that control FGF23K08DK093608 · NIDDK · NEW YORK MEDICAL COLLEGE · PI CHRISTOV, MARTA · 2012 to 2016
$752k
NIDDK NIH HHS K08 DK093608NIDDK NIH HHS K23 DK102511NIDDK NIH HHS K23 DK106448NIDDK NIH HHS P30 DK079337NIDDK NIH HHS R01 DK070910NIDDK NIH HHS R01 DK087727NIDDK NIH HHS R01 DK093574NIDDK NIH HHS U01 DK085660NIDDK NIH HHS Y01 DK003508
6 · The paper itself

Abstract

backgroundIron is a key mediator of AKI in animal models, but data on circulating iron parameters in human AKI are limited.

methodsWe examined results from the ARF Trial Network study to assess the association of plasma catalytic iron, total iron, transferrin, ferritin, free hemoglobin, and hepcidin with 60-day mortality. Participants included critically ill patients with AKI requiring RRT who were enrolled in the study.

resultsOf the 807 study participants, 409 (51%) died by day 60. In both unadjusted and multivariable adjusted models, higher plasma concentrations of catalytic iron were associated with a significantly greater risk of death, as were lower concentrations of hepcidin. After adjusting for other factors, patients with catalytic iron levels in the highest quintile versus the lowest quintile had a 4.06-fold increased risk of death, and patients with hepcidin levels in the lowest quintile versus the highest quintile of hepcidin had a 3.87-fold increased risk of death. These findings were consistent across multiple subgroups. Other iron markers were also associated with death, but the magnitude of the association was greatest for catalytic iron and hepcidin. Higher plasma concentrations of catalytic iron and lower concentrations of hepcidin are each independently associated with mortality in critically ill patients with AKI requiring RRT.

conclusionsThese findings suggest that plasma concentrations of catalytic iron and hepcidin may be useful prognostic markers in patients with AKI. Studies are needed to determine whether strategies to reduce catalytic iron or increase hepcidin might be beneficial in this patient population.

Indexed as

Acute Kidney InjuryAgedBiomarkersCohort StudiesFemaleFerritinsHemoglobinsHepcidinsHumansIronMaleMiddle AgedPrognosisRandomized Controlled Trials as TopicRenal Replacement TherapyRisk FactorsBiomarkersFerritinsHemoglobinsHepcidinsIronTransferrinacute renal failuremortality risknephrotoxicityoutcomes

Identifiers

PMID30737269
PMCPMC6405140
OpenAlexW2912140935

What OpenQuestion holds

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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.