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Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity

Ferric citrate hydrate was recently approved in Japan as an oral phosphate binder to be taken with food for the control of hyperphosphatemia in patients with chronic kidney disease (CKD). The daily therapeutic dose is about 3 to 6 g, which comprises about 2 to 4 g of citrate. Oral citrate solubilize...

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Autor principal: Gupta, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210856/
https://www.ncbi.nlm.nih.gov/pubmed/25341358
http://dx.doi.org/10.3390/ph7100990
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author Gupta, Ajay
author_facet Gupta, Ajay
author_sort Gupta, Ajay
collection PubMed
description Ferric citrate hydrate was recently approved in Japan as an oral phosphate binder to be taken with food for the control of hyperphosphatemia in patients with chronic kidney disease (CKD). The daily therapeutic dose is about 3 to 6 g, which comprises about 2 to 4 g of citrate. Oral citrate solubilizes aluminum that is present in food and drinking water, and opens the tight junctions in the intestinal epithelium, thereby increasing aluminum absorption and urinary excretion. In healthy animals drinking tap water, oral citrate administration increased aluminum absorption and, over a 4-week period, increased aluminum deposition in brain and bone by about 2- and 20-fold, respectively. Renal excretion of aluminum is impaired in patients with chronic kidney disease, thereby increasing the risk of toxicity. Based on human and animal studies it can be surmised that patients with CKD who are treated with ferric citrate hydrate to control hyperphosphatemia are likely to experience enhanced absorption of aluminum from food and drinking water, thereby increasing the risk of aluminum overload and toxicity.
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spelling pubmed-42108562014-10-28 Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity Gupta, Ajay Pharmaceuticals (Basel) Commentary Ferric citrate hydrate was recently approved in Japan as an oral phosphate binder to be taken with food for the control of hyperphosphatemia in patients with chronic kidney disease (CKD). The daily therapeutic dose is about 3 to 6 g, which comprises about 2 to 4 g of citrate. Oral citrate solubilizes aluminum that is present in food and drinking water, and opens the tight junctions in the intestinal epithelium, thereby increasing aluminum absorption and urinary excretion. In healthy animals drinking tap water, oral citrate administration increased aluminum absorption and, over a 4-week period, increased aluminum deposition in brain and bone by about 2- and 20-fold, respectively. Renal excretion of aluminum is impaired in patients with chronic kidney disease, thereby increasing the risk of toxicity. Based on human and animal studies it can be surmised that patients with CKD who are treated with ferric citrate hydrate to control hyperphosphatemia are likely to experience enhanced absorption of aluminum from food and drinking water, thereby increasing the risk of aluminum overload and toxicity. MDPI 2014-09-26 /pmc/articles/PMC4210856/ /pubmed/25341358 http://dx.doi.org/10.3390/ph7100990 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Commentary
Gupta, Ajay
Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity
title Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity
title_full Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity
title_fullStr Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity
title_full_unstemmed Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity
title_short Ferric Citrate Hydrate as a Phosphate Binder and Risk of Aluminum Toxicity
title_sort ferric citrate hydrate as a phosphate binder and risk of aluminum toxicity
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210856/
https://www.ncbi.nlm.nih.gov/pubmed/25341358
http://dx.doi.org/10.3390/ph7100990
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