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The iron cycle in chronic kidney disease (CKD): from genetics and experimental models to CKD patients.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
February 1, 2014
Kimberly Zumbrennen-Bullough et al. (2 authors)
Journal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tReviewHuman Study
Study Details

Study Goal

The researchers aimed to review advances in understanding iron homeostasis in chronic kidney disease (CKD) and explore potential improvements in anemia management for CKD patients.

Results Summary

The abstract highlights dysregulated iron homeostasis in CKD and its role in anemia, noting that iron supplementation is a key treatment but lacks rigorous large-scale trials. Genetic and animal model studies provide insights into iron regulation and potential therapeutic advances.

Population

Chronic kidney disease (CKD) patients

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (2)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Iron supplementation
decrease
anemia
CKD patients
-
is one cornerstone of anemia management
#1
Iron supplementation
neutral
-
CKD patients
-
has not been rigorously studied
#2
Abstract

Iron is essential for most living organisms but iron excess can be toxic. Cellular and systemic iron balance is therefore tightly controlled. Iron homeostasis is dysregulated in chronic kidney disease (CKD) and contributes to the anemia that is prevalent in this patient population. Iron supplementation is one cornerstone of anemia management in CKD patients, but has not been rigorously studied in large prospective randomized controlled trials. This review highlights important advances from genetic studies and animal models that have provided key insights into the molecular mechanisms governing iron homeostasis and its disturbance in CKD, and summarizes how these findings may yield advances in the care of this patient population.

Medical Subject Headings (MeSH)
Anemia, Iron-DeficiencyAnimalsDNADisease ProgressionGene Expression RegulationGenetic Predisposition to DiseaseHepcidinsHomeostasisHumansIronModels, TheoreticalRenal Insufficiency, Chronic
Study Links
Quality Scores
SafetyNot Assessed
Efficacy65/10
Quality70/10
Citation Metrics
Total Citations61
Citations/Year5.5
Relative Citation Ratio2.31
NIH Percentile78.7%
Research Impact Scores
APT Score0.75
Weight Score0.81
Normalized Score0.60
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