Literature DB >> 25565307

Increased plasma catalytic iron in patients may mediate acute kidney injury and death following cardiac surgery.

David E Leaf1, Mohan Rajapurkar2, Suhas S Lele3, Banibrata Mukhopadhyay2, James D Rawn4, Gyorgy Frendl5, Sushrut S Waikar1.   

Abstract

Catalytic iron, the chemical form of iron capable of participating in redox cycling, is a key mediator of acute kidney injury (AKI) in multiple animal models, but its role in human AKI has not been studied. Here we tested in a prospective cohort of 250 patients undergoing cardiac surgery whether plasma catalytic iron levels are elevated and associated with the composite outcome of AKI requiring renal replacement therapy or in-hospital mortality. Plasma catalytic iron, free hemoglobin, and other iron parameters were measured preoperatively, at the end of cardiopulmonary bypass, and on postoperative days 1 and 3. Plasma catalytic iron levels, but not other iron parameters, rose significantly at the end of cardiopulmonary bypass and were directly associated with bypass time and number of packed red blood cell transfusions. In multivariate analyses adjusting for age and preoperative eGFR, patients in the highest compared with the lowest quartile of catalytic iron on postoperative day 1 had a 6.71 greater odds of experiencing the primary outcome, and also had greater odds of AKI, hospital mortality, and postoperative myocardial injury. Thus, our data are consistent with and expand on findings from animal models demonstrating a pathologic role of catalytic iron in mediating adverse postoperative outcomes. Interventions aimed at reducing plasma catalytic iron levels as a strategy for preventing AKI in humans are warranted.

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Year:  2015        PMID: 25565307      PMCID: PMC5137505          DOI: 10.1038/ki.2014.374

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  39 in total

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4.  Effect of surface roughness on hemolysis in a pivot bearing supported Gyro centrifugal pump (C1E3).

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5.  Nitric oxide scavenging by red blood cell microparticles and cell-free hemoglobin as a mechanism for the red cell storage lesion.

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  21 in total

Review 1.  Iron Chelation as a Potential Therapeutic Strategy for AKI Prevention.

Authors:  Shreyak Sharma; David E Leaf
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2.  Iron, Hepcidin, and Death in Human AKI.

Authors:  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
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3.  What's new in trace elements?

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Review 4.  Iron Homeostasis Pathways as Therapeutic Targets in Acute Kidney Injury.

Authors:  Sundararaman Swaminathan
Journal:  Nephron       Date:  2018-07-06       Impact factor: 2.847

Review 5.  Catalytic iron and acute kidney injury.

Authors:  David E Leaf; Dorine W Swinkels
Journal:  Am J Physiol Renal Physiol       Date:  2016-08-17

6.  A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury.

Authors:  Bixiao Zhao; Qiongshi Lu; Yuwei Cheng; Justin M Belcher; Edward D Siew; David E Leaf; Simon C Body; Amanda A Fox; Sushrut S Waikar; Charles D Collard; Heather Thiessen-Philbrook; T Alp Ikizler; Lorraine B Ware; Charles L Edelstein; Amit X Garg; Murim Choi; Jennifer A Schaub; Hongyu Zhao; Richard P Lifton; Chirag R Parikh
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7.  Ferrotoxicity and its amelioration by endogenous vitamin D in experimental acute kidney injury.

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8.  Length Polymorphisms in Heme Oxygenase-1 and AKI after Cardiac Surgery.

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9.  Renal Handling of Circulating and Renal-Synthesized Hepcidin and Its Protective Effects against Hemoglobin-Mediated Kidney Injury.

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Journal:  J Am Soc Nephrol       Date:  2016-01-29       Impact factor: 10.121

Review 10.  Mechanisms of haemolysis-induced kidney injury.

Authors:  Kristof Van Avondt; Erfan Nur; Sacha Zeerleder
Journal:  Nat Rev Nephrol       Date:  2019-08-27       Impact factor: 28.314

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