4.3 Review

Disorders of Iron Metabolism and Anemia in Chronic Kidney Disease

Journal

SEMINARS IN NEPHROLOGY
Volume 36, Issue 4, Pages 252-261

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.semnephrol.2016.05.002

Keywords

Hepcidin; fibroblast growth factor 23; vitamin D; chronic kidney disease; anemia of chronic kidney disease; iron metabolism

Funding

  1. Frommeyer Young Investigator Award
  2. National Institutes of Health [R01NS080850]

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Dysregulated iron homeostasis plays a central role in the development of anemia of chronic kidney disease (CKD) and is a major contributor toward resistance to treatment with erythropoiesis-stimulating agents. Understanding the underlying pathophysiology requires an in-depth understanding of normal iron physiology and regulation. Recent discoveries in the field of iron biology have greatly improved our understanding of the hormonal regulation of iron trafficking in human beings and how its alterations lead to the development of anemia of CKD. In addition, emerging evidence has suggested that iron homeostasis interacts with bone and mineral metabolism on multiple levels, opening up new avenues of investigation into the genesis of disordered iron metabolism in CKD. Building on recent advances in our understanding of normal iron physiology and abnormalities in iron homeostasis in CKD, this review characterizes how anemia related to disordered iron metabolism develops in the setting of CKD. In addition, this review explores our emerging recognition of the connections between iron homeostasis and mineral metabolism and their implications for the management of altered iron status and anemia of CKD. (C) 2016 Elsevier Inc. All rights reserved.

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