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Iron, Hepcidin, and Death in Human AKI.
Leaf, David E; Rajapurkar, Mohan; Lele, Suhas S; Mukhopadhyay, Banibrata; Boerger, Emily A S; Mc Causland, Finnian R; Eisenga, Michele F; Singh, Karandeep; Babitt, Jodie L; Kellum, John A; Palevsky, Paul M; Christov, Marta; Waikar, Sushrut S.
Afiliação
  • Leaf DE; Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts; DELEAF@bwh.harvard.edu.
  • Rajapurkar M; Department of Nephrology.
  • Lele SS; Department of Cardiology, and.
  • Mukhopadhyay B; Department of Biochemistry, Muljibhai Patel Urological Hospital, Gujarat, India.
  • Boerger EAS; Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Mc Causland FR; Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Eisenga MF; Department of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands; Departments of.
  • Singh K; Learning Health Sciences and.
  • Babitt JL; Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
  • Kellum JA; Nephrology Division, Program in Membrane Biology, Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts.
  • Palevsky PM; Center for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Christov M; Renal Section, Veterans Affairs Pittsburgh Healthcare System, Pittsburgh, Pennsylvania.
  • Waikar SS; Renal-Electrolyte Division, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; and.
J Am Soc Nephrol ; 30(3): 493-504, 2019 03.
Article em En | MEDLINE | ID: mdl-30737269
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Injúria Renal Aguda / Hepcidinas / Ferro Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Injúria Renal Aguda / Hepcidinas / Ferro Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article