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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Effect of atorvastatin on iron metabolism regulation in patients with chronic kidney disease - a randomized double
Anna Masajtis-Zagajewska1, Michal Nowicki1
1a Department of Nephrology, Hypertension and Kidney Transplantation , Medical University of Lodz, University Hospital and Teaching Center , Lodz , Poland.
Insights
Atorvastatin therapy in chronic kidney disease (CKD) patients significantly reduced hepcidin and inflammatory markers, potentially improving anemia. Hemojuvelin levels remained unchanged, but iron metabolism showed some positive shifts.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Chronic kidney disease (CKD) is associated with altered iron metabolism and inflammation.
- Hepcidin and hemojuvelin are key regulators of iron homeostasis, often dysregulated in CKD.
- Anemia is a common complication in CKD patients, influenced by iron status and inflammation.
Purpose of the Study:
- To investigate the impact of atorvastatin on hepcidin, hemojuvelin, inflammatory markers, and iron metabolism in CKD stages 3 and 4.
- To assess the potential of atorvastatin in managing anemia in CKD patients.
Main Methods:
- A double-blind, randomized crossover study involving 36 patients with CKD stages 3-4.
- Patients received either atorvastatin or placebo for two 6-month periods.
- Measurements included hepcidin, hemojuvelin, hsCRP, IL-6, hemoglobin, and iron parameters before and after each treatment.
Main Results:
- Atorvastatin significantly decreased hepcidin levels (p < .001) and inflammatory markers (IL-6, hsCRP).
- Hemojuvelin levels did not change. Hemoglobin showed a slight but significant increase (p = .002) with atorvastatin.
- Total iron binding capacity (TIBC) and unsaturated iron binding capacity (UIBC) increased, with a trend towards increased serum iron.
Conclusions:
- Atorvastatin demonstrates a potentially beneficial effect on serum hepcidin in CKD patients.
- This reduction in hepcidin may contribute to improved anemia control in this population.
- Further research is warranted to confirm the long-term benefits of statin therapy on iron metabolism and anemia in CKD.
Introduction:
To determine the effect of 6-month administration of atorvastatin on hepcidin and hemojuvelin levels, inflammatory parameters and iron metabolism in patients with chronic kidney disease (CKD) stages 3 and 4.
Methods:
Thirty six statin- and erythropoiesis-stimulating agent-naive patients with CKD stages 3 and 4 and LDL cholesterol ≥100 mg/dl received atorvastatin or placebo for two 6-month periods in a double blind, randomized crossover study. Hepcidin, hemojuvelin, hsCRP, IL-6, hemoglobin, red blood cell distribution width, iron, total iron binding capacity (TIBC), and unsaturated iron binding capacity (UIBC) were measured before and after each treatment period.
Results:
Hepcidin decreased (from 102 [307] to 63 [170] pg/ml (p > .001)) in the course of statin therapy but remained unchanged after placebo administration (173 [256] to 153 [204] pg/ml, respectively). Hemojuvelin did not change after either part of the study. Both IL-6 and hsCRP decreased following statin therapy (from 8.7 [12.0] to 8.1 [13.9] pg/ml; p = .04 and from 4.7 [4.0] to 4.0 [3.6] mg/l; p = .4, respectively), but did not change after placebo administration. Blood hemoglobin increased slightly but significantly after 6-month statin therapy (from 11.6 ± 1.6 to 11.9 ± 1.5 g/dl, p = .002), and was unchanged after placebo treatment. TIBC and UIBC increased significantly after 6-month statin therapy, and serum iron also tended to increase. The change of eGFR during the study did not differ between the two treatment periods.
Conclusions:
Statin may have a small but potentially beneficial effect on serum hepcidin, which may lead to improvement of anemia control in CKD patients.
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