Long-Term Effect of Ferric Citrate Hydrate on Mineral Metabolism and Anemia in Maintenance Hemodialysis Patients
- 1 Department of Nephrology, Jyoban Hospital, Fukushima, Japan
- 2 Department of Nephrology, Jyoban Hospital, Fukushima, Japan
- 3 Department of Nephrology, Jyoban Hospital, Fukushima, Japan
- 4 Department of Nephrology, Jyoban Hospital, Fukushima, Japan
- 5 Department of Nephrology, Tokyo Women’s Medical University, Tokyo, Japan
Abstract
Background: Ferric citrate hydrate is a phosphate (P)-binder drug that is indicated for patients with chronic kidney disease (CKD) undergoing maintenance hemodialysis (MHD). Objectives: The objectives of this study were to evaluate the changes in the serum mineral metabolism biomarker levels and treatment status of anemia in MHD patients receiving ferric citrate hydrate. Methods: A total of 132 adult dialysis patients were enrolled in this study. Bone turnover marker levels, anemia status and iron biomarker levels over a period of 18 months after the start of the ferric citrate hydrate treatment were extracted from the medical records of the patients. Results: At enrollment, 14 (10.6%) patients were P-binder-na ï ve, and 118 (89.4%) patients were receiving other P-binders. The serum P level before the start of ferric citrate hydrate treatment was ≤5.5 mg/dL in 18.8% of the patients. After 18 months of ferric citrate hydrate treatment, the proportion of patients with serum P levels ≤ 5.5 mg/dL increased to 47.7%. The mean ± standard error of the mean (SEM) of the serum P level was 7.05 ± 0.14 mg/dL at the baseline, and decreased to 5.83 ± 0.17 mg/dL after 18 months of treatment with ferric citrate hydrate. The mean ± SEM of the serum hemoglobin (Hb), ferritin, and transferrin saturation (TSAT) levels were 11.96 ± 0.76 g/dL, 71.13 ± 6.09 ng/mL, and 25.19% ± 1.21%, respectively, at the baseline, and 11.45 ± 0.13 g/dL, 124.94 ± 8.62 ng/mL, and 26.18% ± 0.99%, respectively, after 18 months of ferric citrate hydrate treatment. Conclusions: These results suggest that the serum P and anemia biomarker levels observed in this study were similar to those reported in clinical trials.
- Coladonato, J.A. (2005) Control of Hyperphosphatemia among Patients with ESRD. Journal of American Society of Nephrology, 16, S1107-S1114. https://doi.org/10.1681/ASN.2005060663
- Noordzij, M., Korevaar, J.C., Boeschoten, E.W., Dekker, F.W., Bos, W.J. and Krediet, R.T. (2006) Hyperphosphataemia and Related Mortality. Nephrology Dialysis Transplantation, 21, 2676-2677. https://doi.org/10.1093/ndt/gfl229
- Isakova, M., Gutierrez, O.M., Chang, Y., Shah, A., Tamez, H., Smith, K., Thadhari, R. and Wolf. M. (2009) Phosphorus Binders and Survival on Hemodialysis. Journal of American Society of Nephrology, 20, 388-396. https://doi.org/10.1681/ASN.2008060609
- Yokoyama, K., Hirakata, H., Akiba, T., Sawada, K. and Kumagai, Y. (2012) Effect of Oral JTT-751 (Ferric Citrate) on Hyperphosphatemia in Hemodialysis Patients: Results of a Randomized, Double-Blind, Placebo-Controlled Trial. American Journal of Nephrology, 36, 478-487. https://doi.org/10.1159/000344008
- Yokoyama, K., Akiba, T., Fukagawa, M., Nakayama, M., Sawada, K., Kumagai, Y., Chertow, G.M. and Hirakata, H. (2014) A Randomized Trial of JTT-751 versus Sevelamer Hydrochloride in Patients on Hemodialysis. Nephrology Dialysis Transplantation, 29, 1053-1060. https://doi.org/10.1093/ndt/gft483
- Uhlig, K., Berns, J.S., Kestenbaum, B., Kumar, R., Leonard, M.B., Martin, K.J., Sprague, S.M. and Goldfarb, S. (2010) KDOQI US Commentary on the 2009 KDIGO Clinical Practice Guideline for the Diagnosis, Evaluation, and Treatment of CKD-Mineral and Bone Disorder (CKD-MBD). American Journal of Kidney Diseases, 7, 3-6. https://doi.org/10.1053/j.ajkd.2010.02.340
- Okazaki, M., Komatsu, M., Kawaguchi, H. and Nitta, K. (2014) Erythropoietin Resistance Index and the All-Cause Mortality of Chronic Hemodialysis Patients. Blood Purification, 37, 106-112. https://doi.org/10.1159/000358215
- Yokoyama, K., Fukagawa, M., Akiba, T., Nakayama, M., Otoguro, T., Yamada, K., Nagamine, Y., Fishbane, S. and Hirakata, H. (2017) Ferritin Elevation and Improved Responsiveness to Erythropoiesis-Stimulating Agents in Patients on Ferric Citrate Hydrate. Kidney International Reports, 2, 359-365. https://doi.org/10.1016/j.ekir.2016.12.005
- Blayney, M.J. and Tentori, F. (2009) Trends and Consequences of Mineral Bone Disorder in Haemodialysis Patients: Lessons from the Dialysis Outcomes and Practice Patterns Study (DOPPS). Journal of Renal Care, 35, 7-13. https://doi.org/10.1111/j.1755-6686.2009.00048.x
- Yokoyama, K., Fukagawa, M., Akiba, T., Nakayama, M., Ito, K., Hanaki, K., Wolf, M. and Hirakata, H. (2019) Randomised Clinical Trial of Ferric Citrate Hydrate on Anaemia Management in Haemodialysis Patients with Hyperphosphataemia: ASTRIO Study. Scientific Reports, 9, 8877. https://doi.org/10.1038/s41598-019-45335-4