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Lanthanum: a safe phosphate binder.
Veerle P Persy1, Geert J Behets, An R Bervoets
1University of Antwerp, Antwerp, Belgium. veerle.persy@ua.ac.be
Seminars in Dialysis
|May 13, 2006
Summary
Lanthanum carbonate effectively manages hyperphosphatemia in dialysis patients without increasing calcium load. Studies show no toxic effects, with the liver being the primary excretion route and no lanthanum detected in brain tissue.
Area of Science:
- Nephrology
- Pharmacology
- Toxicology
Background:
- Elevated inorganic phosphate in dialysis patients contributes to cardiovascular mortality and vascular calcification.
- Traditional calcium-based phosphate binders and vitamin D may increase calcium-phosphate product, raising ectopic mineralization risks.
- Calcium-free phosphate binders offer an alternative to manage hyperphosphatemia without augmenting calcium load.
Purpose of the Study:
- To discuss the metabolism and effects of lanthanum carbonate, a calcium-free phosphate binder.
- To evaluate the safety profile of lanthanum carbonate in bone, liver, and brain.
- To compare lanthanum's effects with other metal cations like aluminum.
Main Methods:
- Review of clinical studies and preclinical data on lanthanum carbonate.
- Analysis of lanthanum's pharmacokinetic and toxicological profile.
- Investigation of lanthanum distribution and effects in target organs.
Main Results:
- Lanthanum carbonate effectively controls hyperphosphatemia without increasing patient calcium load.
- Clinical studies show no toxic effects of lanthanum carbonate up to four years.
- Lanthanum exhibits extremely low bioavailability; observed bone effects are due to phosphate depletion, not direct toxicity.
- The liver is the primary route of lanthanum excretion, localized in hepatocyte lysosomes.
- No lanthanum was detected in brain tissue.
Conclusions:
- Lanthanum carbonate is a safe and effective calcium-free phosphate binder for dialysis patients.
- Its low bioavailability and specific excretion pathway contribute to a favorable safety profile.
- Further research supports its use in managing renal failure-associated hyperphosphatemia.