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An assessment of cinacalcet HCl effects on bone histology in dialysis patients with secondary hyperparathyroidism

Title
An assessment of cinacalcet HCl effects on bone histology in dialysis patients with secondary hyperparathyroidism
Type
Article in International Scientific Journal
Year
2008
Authors
Malluche, HH
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Monier Faugere, MC
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Wang, G
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João Frazão
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Charytan, C
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Coburn, JW
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Coyne, DW
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Kaplan, MR
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Baker, N
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McCary, LC
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Turner, SA
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Goodman, WG
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Journal
Title: Clinical NephrologyImported from Authenticus Search for Journal Publications
Vol. 69
Pages: 269-278
ISSN: 0301-0430
Other information
Authenticus ID: P-004-0B1
Abstract (EN): Aims: Cinacalcet lowers plasma parathyroid hormone (PTH) levels in patients with secondary hyperparathyroidism (sHPT), but the bone histologic response has not been described. This prospective, double-blind, placebo-controlled trial assessed the effects of cinacalcet on bone histology and serum markers of bone metabolism in dialysis patients with sHPT. Methods: Patients with intact PTH (iPTH) >= 300 pg/ml were randomly assigned 2:1 to receive cinacalcet or placebo with concurrent vitamin D and/or phosphate bindertherapy. Cinacalcet (30-180 mg/day) was used to achieve iPTH levels! 200 pg/ml. Bone biopsies were performed before and after one year of treatment. Results: Baseline and end-of-study data were available from 32 patients (19 cinacalcet, 13 placebo). Baseline bone tunnover was elevated in 27, reduced in 3 and normal in 2 patients. Serum bone-specific alkaline phosphatase (BSAP) and N-telopeptide (NTx) were elevated. Cinacalcet treatment decreased PTH and diminished activation frequency, bone formation rate/bone surface, and fibrosis surface/bone surface. Adynamic bone was observed in three patients receiving cinacalcet; in two of these, PTH levels were persistently low (< 100 pg/ml). The histomorphometric parameter changes in bone corresponded to PTH, BSAP and NTx reductions. Bone mineralization parameters remained normal. Conclusions: Treatment with cinacalcet lowered PTH and reduced bone turnover and tissue fibrosis among most dialysis patients with biochemical evience of sHPT.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 10
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