Oncotarget

Meta-Analysis:

Safety and efficacy of ferric citrate in phosphate reduction and iron supplementation in patients with chronic kidney disease

Mei-Yi Wu, Ying-Chun Chen, Chun-Hung Lin, Yun-Chun Wu, Yu-Kang Tu and Der-Cherng Tarng _

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Oncotarget. 2017; 8:107283-107294. https://doi.org/10.18632/oncotarget.21990

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Abstract

Mei-Yi Wu1,2,3, Ying-Chun Chen4, Chun-Hung Lin5, Yun-Chun Wu3, Yu-Kang Tu3 and Der-Cherng Tarng6,7,8

1Division of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, Taipei, Taiwan

2Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

3Graduate Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan

4Department of Pharmacy, Taipei Medical University, Shuang Ho Hospital, Taipei, Taiwan

5Department of Education, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

6Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan

7Department and Institute of Physiology, National Yang-Ming University, Taipei, Taiwan

8Division of Nephrology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan

Correspondence to:

Der-Cherng Tarng, email: [email protected], [email protected]

Keywords: ferric citrate, chronic kidney disease, phosphate binder, anemia, meta-analysis

Received: August 16, 2017     Accepted: September 20, 2017     Published: October 20, 2017

ABSTRACT

Ferric citrate has been reported to have the potential to reduce phosphate and increase iron availability in patients with chronic kidney disease. In the present study, we evaluated its safety and efficacy in phosphate reduction and iron supplementation in chronic kidney disease stage 3-5 requiring dialysis patients. We systematically searched for clinical trials published in PubMed, Medline, and Cochrane databases. Only randomized controlled trials on the effects of ferric citrate in chronic kidney disease stage 3–5 requiring dialysis patients were selected. The primary outcomes were changes in serum phosphate, calcium, and anemia-related parameters. The secondary outcomes were the adverse effects of ferric citrate. Nine studies providing data on 1755 patients were included in the meta-analysis. Ferric citrate significantly reduced serum phosphate compared with placebo (mean difference, –1.39; 95% confidence interval, –2.12 to –0.66) and had a non-inferior effect compared with active treatment. Furthermore, ferric citrate significantly improved hemoglobin, transferrin saturation and ferritin. Adverse effects of constipation did not differ significantly between ferric citrate and placebo or active treatment. This review provides evidence that ferric citrate effectively alleviates hyperphosphatemia and iron deficiency in patients with chronic kidney disease stage 3–5 requiring dialysis patients. However, the included studies did not have cardiovascular complications or mortality information and could not assess whether ferric citrate affected the risk of all-cause death or cardiovascular complications in patients with chronic kidney disease. Further studies are required to assess whether the long-term use of ferric citrate can reduce the risk of cardiovascular events and all-cause mortality.


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