Abstract

BackgroundIt is controversial for the effect and safety between cinacalcet and other treatments in treating secondary hyperparathyroidism for patients with chronic kidney disease (CKD) or end-stage renal disease (ESRD).MethodsEmbase, PubMed, and Cochrane Library were searched through Feb 2017. 21 randomized controlled trials were included. We calculated the pooled mean difference (MD), relative risk (RR) and corresponding 95% confidence interval (CI).ResultPatients received calcimimetic agents had significantly decreased serum parathyroid hormone (MD = − 259.24 pg/mL, 95% CI: − 336.23 to − 182.25), calcium (MD = − 0.92 mg/dL, 95% CI: − 0.98 to − 0.85) and calcium phosphorus product (MD = − 5.97 mg2/dL2, 95% CI: − 9.77 to − 2.16) concentration compared with control treatment. However, the differences in cardiovascular mortality and all-cause mortality between calcimimetics agents and control group were not statistically significant. The incidence of nausea (RR = 2.13, 95% CI: 1.62 to 2.79), vomiting (RR = 1.99, 95% CI: 1.78 to 2.23) and hypocalcemia (RR = 10.10, 95% CI: 7.60 to 13.43) in CKD patients with calcimimetics agents was significantly higher than that with control treatment.ConclusionCinacalcet improved the biochemical parameters in CKD patients, but did not improve all-cause mortality and cardiovascular mortality. Moreover, cinacalcet can cause some adverse events.

Highlights

  • It is controversial for the effect and safety between cinacalcet and other treatments in treating secondary hyperparathyroidism for patients with chronic kidney disease (CKD) or end-stage renal disease (ESRD)

  • Cinacalcet improved the biochemical parameters in CKD patients, but did not improve all-cause mortality and cardiovascular mortality

  • Cinacalcet acts by increasing the sensitivity of the calcium-sensing receptor (CaSR) on parathyroid cells to extracellular calcium ion levels, thereby decreasing serum parathyroid hormone (PTH) without increasing serum calcium, phosphate or the calcium phosphate product (Ca × P) in secondary hyperparathyroidism (SHPT) patients [4, 5]

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Summary

Introduction

It is controversial for the effect and safety between cinacalcet and other treatments in treating secondary hyperparathyroidism for patients with chronic kidney disease (CKD) or end-stage renal disease (ESRD). Cardiovascular (CV) events in patients with chronic kidney disease (CKD) occur frequently [1]. CKD patient population experiences a high burden of cardiovascular mortality etyjhigher than general population. There are many causes of CV disease in chronic kidney disease, but mineral and bone disorder (MBD), including hyperphosphatemia, secondary hyperparathyroidism (SHPT) and vascular calcification. Cinacalcet, an orally administered calcimimetic agent was originally approved in 2004 for the treatment of SHPT in patients with ESRD [4]. Cinacalcet acts by increasing the sensitivity of the calcium-sensing receptor (CaSR) on parathyroid cells to extracellular calcium ion levels, thereby decreasing serum PTH without increasing serum calcium, phosphate or the calcium phosphate product (Ca × P) in SHPT patients [4, 5]. Cinacalcet lowers serum fibroblast growth factor-23 (FGF23) levels in haemodialysis patients

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