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Clinical Research
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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, Paul M. Palevsky, Marta Christov and Sushrut S. Waikar
JASN February 2019, ASN.2018100979; DOI: https://doi.org/10.1681/ASN.2018100979
David E. Leaf
Division of Renal Medicine, Brigham and Women’s Hospital, Boston, Massachusetts;
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Mohan Rajapurkar
Department of Nephrology,
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Suhas S. Lele
Department of Cardiology, and
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Banibrata Mukhopadhyay
Department of Biochemistry, Muljibhai Patel Urological Hospital, Gujarat, India;
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Emily A.S. Boerger
Division of Renal Medicine, Brigham and Women’s Hospital, Boston, Massachusetts;
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Finnian R. Mc Causland
Division of Renal Medicine, Brigham and Women’s Hospital, Boston, Massachusetts;
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Michele F. Eisenga
Department of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands; Departments of
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Karandeep Singh
Learning Health Sciences andInternal Medicine, University of Michigan Medical School, Ann Arbor, Michigan;
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Jodie L. Babitt
Nephrology Division, Program in Membrane Biology, Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts;
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John A. Kellum
Center for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania;
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Paul M. Palevsky
Renal Section, Veterans Affairs Pittsburgh Healthcare System, Pittsburgh, Pennsylvania;Renal-Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; and
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Marta Christov
Department of Medicine, New York Medical College, Valhalla, New York
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Sushrut S. Waikar
Division of Renal Medicine, Brigham and Women’s Hospital, Boston, Massachusetts;
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Significance Statement

Dysregulated iron metabolism plays an important pathogenic role in AKI in animal models, but limited data are available on circulating iron parameters in human AKI. To assess the association of plasma catalytic iron, total iron, transferrin, TSAT, ferritin, free hemoglobin, and hepcidin with 60-day mortality, the authors examined observations in a cohort study of 807 critically ill patients with AKI (all requiring RRT) who were enrolled the ARF Trial Network study. They found that higher concentrations of catalytic iron and lower concentrations of hepcidin are each monotonically and independently associated with increased mortality. These findings identify plasma catalytic iron and hepcidin as potentially useful prognostic markers or therapeutic targets in patients with AKI requiring RRT.

Abstract

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

Methods We 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.

Results Of 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.

Conclusions These 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.

  • acute renal failure
  • mortality risk
  • nephrotoxicity
  • outcomes
  • Copyright © 2019 by the American Society of Nephrology
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Journal of the American Society of Nephrology: 30 (2)
Journal of the American Society of Nephrology
Vol. 30, Issue 2
February 2019
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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, Paul M. Palevsky, Marta Christov, Sushrut S. Waikar
JASN Feb 2019, ASN.2018100979; DOI: 10.1681/ASN.2018100979

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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, Paul M. Palevsky, Marta Christov, Sushrut S. Waikar
JASN Feb 2019, ASN.2018100979; DOI: 10.1681/ASN.2018100979
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Keywords

  • acute renal failure
  • mortality risk
  • nephrotoxicity
  • outcomes

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