4.7 Article

Iron: Innocent bystander or vicious culprit in COVID-19 pathogenesis?

Journal

INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES
Volume 97, Issue -, Pages 303-305

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ijid.2020.05.110

Keywords

Hyper-ferritinemia; Hypercoagulability; Iron homeostasis; Ferroptosis; Oxidative stress; Mitochondria

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The coronavirus 2 (SARS-CoV-2) pandemic is viciously spreading through the continents with rapidly increasing mortality rates. Current management of COVID-19 is based on the premise that respiratory failure is the leading cause of mortality. However, mounting evidence links accelerated pathogenesis in gravely ill COVID-19 patients to a hyper-inflammatory state involving a cytokine storm. Several components of the heightened inflammatory state were addressed as therapeutic targets. Another key component of the heightened inflammatory state is hyper-ferritinemia which reportedly identifies patients with increased mortality risk. In spite of its strong association with mortality, it is not yet clear if hyper-ferritinemia in COVID-19 patients is merely a systemic marker of disease progression, or a key modulator in disease pathogenesis. Here we address implications of a possible role for hyper-ferritinemia, and altered iron homeostasis in COVID-19 pathogenesis, and potential therapeutic targets in this regard. (c) 2020 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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