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Role of Hepcidin in Heart Failure with Iron Deficiency - Deception or Disposition
Gaurav Saxena1, Peyush Khera2, Deepak Jain3
1Senior Professor & Head,Department of Medicine and Division of Nephrology, Pt. B.D. Sharma University of Health Sciences, Rohtak, Haryana; *Corresponding Author.
Insights
Ferric citrate effectively lowers phosphate levels and improves anemia in chronic kidney disease (CKD) patients. This study shows significant improvements in phosphate, hemoglobin, ferritin, and transferrin saturation in CKD patients after three months of ferric citrate treatment.
Area of Science:
- Nephrology
- Hematology
- Biochemistry
Background:
- Chronic kidney disease (CKD) is linked to mineral and bone disorders, increasing risks of cardiovascular calcification and osteoporosis.
- Anemia is common in CKD, associated with disease progression and mortality.
- Ferric citrate, a novel oral phosphate binder, also addresses iron deficiency in CKD patients.
Purpose of the Study:
- To evaluate the efficacy of ferric citrate as a phosphate binder in pre-dialysis CKD patients.
- To assess the impact of ferric citrate on hematologic parameters, including iron status.
Main Methods:
- A prospective study involving 40 pre-dialysis adult CKD patients (stage 3-5).
- Patients received ferric citrate (1.1 gm tablets, 3 times daily) for three months.
- Exclusion criteria included prior use of intravenous iron or erythropoiesis-stimulating agents.
Main Results:
- Significant reduction in mean serum phosphate from 6.55±0.70 mg/dl to 4.36±0.50 mg/dl (p<0.001).
- Mean hemoglobin increased from 7.92±1.05 g/dl to 10.96±1.04 g/dl (p<0.001).
- Serum ferritin and transferrin saturation also showed significant increases.
Conclusions:
- Ferric citrate is an effective and well-tolerated phosphate binder for CKD patients.
- Ferric citrate significantly improves hematologic parameters, addressing anemia and iron deficiency in CKD.
Introduction:
Disorders of mineral and bone metabolism in chronic kidney disease (CKD) are associated with increased risk for cardiovascular calcification and osteoporosis. Anemia has been associated with progressive loss of kidney function and increased mortality. Ferric citrate was recently developed, primarily as a novel oral, non-calcium phosphate binder, which has also shown to replenish the iron deficient state of the CKD patients.
Material And Methods:
This prospective study was done on 40 pre-dialysis adult patients of CKD (stage 3-5) from a tertiary care centre in North India. Patients on intravenous iron, erythropoietin stimulating agents or other phosphate binders were excluded from the study. All the patients were given tablet ferric citrate (each tablet containing ferric citrate 1.1 gm equivalent to ferric iron 210 mg) in a dose of 3 tablets per day for three months. Patients were followed up at two weekly intervals and relevant investigations were done. They were divided into three groups according to their CKD stages for subgroup analysis.
Observations:
After three months of therapy with ferric citrate there was a significant decrease in mean serum phosphate from 6.55±0.70 mg/dl at baseline to 4.36±0.50 mg/dl at the end of three months (p<0.001). Mean hemoglobin increased from 7.92±1.05 g/dl at baseline to 10.96±1.04 g/dl at the end of three months (p<0.001). Serum ferritin and serum transferrin saturation increased from 278.25±110.56 ng/dl, 25.02±4.03 % at baseline to 401.24±152.47 ng/dl and 29.62±3.77 % at the end of three months. The mean serum vitamin D and serum iPTH levels, at baseline and at the end of 3 months were 14.61±10.80 ng/ml, 509.48±210.75 pg/ml and 23.65±14.00 ng/ml, 424.14±173.18 pg/ml respectively. The change in all these parameters were significant irrespective of the CKD stages.
Conclusion:
The present study has shown that ferric citrate is an effective and well tolerated phosphate binder, which also significantly improves hematologic parameters in an iron deficient CKD patient.
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