Abstract

BackgroundSecondary hyperparathyroidism (SHPT) is a common complication in chronic kidney disease (CKD) patients. Cinacalcet could be a therapeutic option although its use is controversial in patients not receiving dialysis. Thus, the aim of this study is to assess the effectiveness and safety of cinacalcet in patients with CKD and SHPT without renal replacement treatment (RRT) and without renal transplantation (RT).MethodsA retrospective observational study was conducted. Patients were included if they had collected cinacalcet, under off-label use, during 2010 and 2011. Patients selected were followed from the beginning of cinacalcet therapy for one year of treatment.ResultsA total of 37 patients were included with CKD stage 3 (38%), 4 (51%) and 5 (11%). Baseline mean PTH value was 400.86 ± 168.60 mg/dl. At 12 months, a 67% of patients achieved at least a 30% reduction in their PTH value (p<0.001; CI 49.7–83.6), and the overall mean reduction of PTH values was 38% (p< 0.001; IC -49.1, -27.5). A 28% of the patients achieved KDOQI PTH goals (p = 0.003, CI 12%-50%). At 12 months, mean serum calcium values decreased by 6% and mean serum phosphorus values increased by 13%. A 19% of patients experienced hypocalcemia episodes while an increase of 24% in hyperphosphatemia episodes was observed. A 25% of patients finished cinacalcet before a year of treatment. Main withdrawal reasons were: gastrointestinal and other discomfort (8%), hypocalcaemia (8%), non-compliance (3%), interactions (3%) and excess of efficacy (3%).ConclusionsCinacalcet was effective in patients with CKD and SHPT not receiving dialysis. Electrolytic imbalances could be managed with administration of vitamin D and analogues or phosphate binders.

Highlights

  • Cinacalcet was effective in patients with chronic kidney disease (CKD) and Secondary hyperparathyroidism (SHPT) not receiving dialysis

  • Secondary hyperparathyroidism (SHPT) is a complication of chronic kidney disease (CKD) that develops in the early stages and worsens as kidney function deteriorates

  • SHPT is caused by reduced phosphate excretion that leads to an increase of fibroblast growth factor-23, a reduced synthesis of 1,25-dihydroxy vitamin D and hypocalcemia, all of which promote parathyroid hormone (PTH) synthesis and release [1]

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Summary

Introduction

Secondary hyperparathyroidism (SHPT) is a complication of chronic kidney disease (CKD) that develops in the early stages and worsens as kidney function deteriorates. SHPT is caused by reduced phosphate excretion that leads to an increase of fibroblast growth factor-23, a reduced synthesis of 1,25-dihydroxy vitamin D and hypocalcemia, all of which promote parathyroid hormone (PTH) synthesis and release [1]. PTH values increase to restore calcium and phosphorus homeostasis. Available treatment options include diet phosphorus restriction, vitamin D and analogues, phosphate binders, calcimimetics and, in severe cases, parathyroidectomy [1,2,3,4]. Cinacalcet hydrochloride (Amgen, Thousand Oaks, CA, United States) is a type II calcimimetic that increases the sensitivity to extracellular calcium of the calcium-sensing receptor (CaR) located in chief cells of parathyroid gland, thereby reducing PTH synthesis and release [4]. Secondary hyperparathyroidism (SHPT) is a common complication in chronic kidney disease (CKD) patients. The aim of this study is to assess the effectiveness and safety of cinacalcet in patients with CKD and SHPT without renal replacement treatment (RRT) and without renal transplantation (RT)

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