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Role of Cinacalcet in Management of Mineral Bone Disorder in Chronic Kidney Disease (Control of Calcium, Phosphorus and Parathyroid Hormone)
Author(s) -
Tahara Hideki
Publication year - 2008
Publication title -
therapeutic apheresis and dialysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.415
H-Index - 53
eISSN - 1744-9987
pISSN - 1744-9979
DOI - 10.1111/j.1744-9987.2008.00628.x
Subject(s) - cinacalcet , medicine , parathyroid hormone , hyperphosphatemia , secondary hyperparathyroidism , vitamin d and neurology , endocrinology , kidney disease , hyperparathyroidism , calcium , bone mineral , osteoporosis
The management of hemodialysis patients with chronic kidney disease–mineral bone disorder includes treatment to control levels of calcium, phosphorus and parathyroid hormone, so as to prevent bone and soft‐tissue complications. Recently, pleiotropic effects of active vitamin D have attracted much attention, and its effect on outcome has also gained recognition. However, administration of active vitamin D may cause hypercalcemia and hyperphosphatemia. Now, the use of a novel class of drugs, cinacalcet hydrochloride, has been proposed as a strategy to reduce parathyroid hormone secretion, while decreasing levels of serum calcium, phosphorus, and calcium × phosphorus products. Among subjects with secondary hyperparathyroidism undergoing hemodialysis, combined therapy with cinacalcet and vitamin D sterols improved achievement of the biochemical targets for chronic kidney disease–mineral bone disorder recommended by the guidelines.