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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Erythropoiesis-independent effects of iron in chronic kidney disease
Edwin Patino1, Oleh Akchurin2,3
1Department of Medicine, Division of Nephrology and Hypertension, Weill Cornell Medical College, New York, NY, USA.
Insights
Chronic kidney disease (CKD) alters iron metabolism, impacting anemia and requiring iron supplementation. Iron therapy in CKD has wide-ranging effects beyond blood, influencing inflammation, fibrosis, and bone health.
Area of Science:
- Nephrology
- Hematology
- Biochemistry
Background:
- Chronic kidney disease (CKD) is associated with disturbed iron metabolism.
- Elevated hepcidin levels in CKD patients cause significant iron redistribution.
- Anemia is a common complication of CKD, often requiring iron supplementation.
Purpose of the Study:
- To review the pleiotropic effects of iron supplementation in CKD.
- To explore the impact of iron on various organ systems beyond hematologic effects.
- To discuss novel applications of iron therapy in CKD management.
Main Methods:
- Literature review of recent data on iron metabolism and supplementation in CKD.
- Analysis of the effects of iron on inflammation, oxidative stress, fibrosis, cardiovascular disease, and bone and mineral disorders.
- Examination of iron-based phosphate binders as a dual-indication therapy.
Main Results:
- Iron supplementation in CKD has effects beyond anemia, influencing inflammation, oxidative stress, kidney fibrosis, cardiovascular health, and bone-mineral disorders.
- The route of administration and specific iron preparation significantly impact these effects.
- Iron-based phosphate binders offer a novel approach for treating both anemia and hyperphosphatemia.
Conclusions:
- Optimizing iron therapy in CKD can lead to new strategies for managing complications.
- Iron supplementation may play a role in modifying CKD progression.
- Further research into iron's multifaceted roles is crucial for advancing CKD care.
Abstract:
Chronic kidney disease (CKD) leads to alterations of iron metabolism, which contribute to the development of anemia and necessitates iron supplementation in patients with CKD. Elevated hepcidin accounts for a significant iron redistribution in CKD. Recent data indicate that these alterations in iron homeostasis coupled with therapeutic iron supplementation have pleiotropic effects on many organ systems in patients with CKD, far beyond the traditional hematologic effects of iron; these include effects of iron on inflammation, oxidative stress, kidney fibrosis, cardiovascular disease, CKD-mineral and bone disorder, and skeletal growth in children. The effects of iron supplementation appear to be largely dependent on the route of administration and on the specific iron preparation. Iron-based phosphate binders exemplify the opportunity for using iron for both traditional (anemia) and novel (hyperphosphatemia) indications. Further optimization of iron therapy in patients with CKD may inform new approaches to the treatment of CKD complications and potentially allow modification of disease progression.
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