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Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis

BACKGROUND: The elevated calcium and phosphorus levels in patients undergoing hemodialysis may increase the risk of all-cause mortality. Paricalcitol, as a new vitamin D receptor activator (VDRA), seemed to be effective in reducing the calcium and phosphorus levels. OBJECTIVES: The aim of this study...

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Autores principales: Liu, Yang, Liu, Ling-Yun, Jia, Ye, Wu, Mei-Yan, Sun, Yan-Yan, Ma, Fu-Zhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445244/
https://www.ncbi.nlm.nih.gov/pubmed/30992658
http://dx.doi.org/10.2147/DDDT.S176257
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author Liu, Yang
Liu, Ling-Yun
Jia, Ye
Wu, Mei-Yan
Sun, Yan-Yan
Ma, Fu-Zhe
author_facet Liu, Yang
Liu, Ling-Yun
Jia, Ye
Wu, Mei-Yan
Sun, Yan-Yan
Ma, Fu-Zhe
author_sort Liu, Yang
collection PubMed
description BACKGROUND: The elevated calcium and phosphorus levels in patients undergoing hemodialysis may increase the risk of all-cause mortality. Paricalcitol, as a new vitamin D receptor activator (VDRA), seemed to be effective in reducing the calcium and phosphorus levels. OBJECTIVES: The aim of this study was to compare the efficacy and safety of paricalcitol with other VDRAs in patients undergoing hemodialysis. METHODS: PubMed, Embase, and Web of Science database were systematically reviewed. SELECTION CRITERIA: Studies that focused on the use of paricalcitol for hemodialysis patients were eligible for inclusion. DATA COLLECTION AND ANALYSIS: Two independent investigators performed the literature search, data extraction, and assessment of methodological quality. The outcomes were expressed with standard mean difference (SMD), HR, or risk ratio (RR) with 95% CI. RESULTS: Thirteen studies involving 112,695 patients were included in this meta-analysis. Among these studies, four studies were cohort studies and nine studies were randomized controlled trials (RCTs). For cohort studies, they were regarded as being of high quality; for RCTs, only one was classified as being at low risk of bias; and the remaining eight studies were at being unclear risk of bias. Compared with other VDRAs, paricalcitol significantly improved the overall survival (HR =0.86, 95% CI: 0.80, 0.92; P<0.001) and reduced the intact parathyroid hormone (iPTH) (SMD =−0.53, 95% CI: −0.90, −0.17; P=0.004). Paricalcitol offered similar effect with other VDRAs in the control of calcium (SMD =0.32, 95% CI: −0.04, 0.67; P=0.078) and phosphorus (SMD =0.06, 95% CI: −0.26, 0.37; P=0.727) levels. However, the serum change in calcium phosphate product was greater in the paricalcitol group than in the other VDRA group (SMD =2.13, 95% CI: 0.19, 4.07; P=0.031). There was no significant difference in the incidence of adverse events between the two groups (RR =1.02, 95% CI: 0.93, 1.12; P=0.674). CONCLUSION: Paricalcitol was crucial in reducing the mortality in patients undergoing hemodialysis. Moreover, both paricalcitol and other VDRAs were effective in control of the serum iPTH, calcium, and phosphorus levels. Given the potential limitations in this study, more prospective large-scale, well-conducted RCTs are needed to confirm these findings.
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spelling pubmed-64452442019-04-16 Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis Liu, Yang Liu, Ling-Yun Jia, Ye Wu, Mei-Yan Sun, Yan-Yan Ma, Fu-Zhe Drug Des Devel Ther Original Research BACKGROUND: The elevated calcium and phosphorus levels in patients undergoing hemodialysis may increase the risk of all-cause mortality. Paricalcitol, as a new vitamin D receptor activator (VDRA), seemed to be effective in reducing the calcium and phosphorus levels. OBJECTIVES: The aim of this study was to compare the efficacy and safety of paricalcitol with other VDRAs in patients undergoing hemodialysis. METHODS: PubMed, Embase, and Web of Science database were systematically reviewed. SELECTION CRITERIA: Studies that focused on the use of paricalcitol for hemodialysis patients were eligible for inclusion. DATA COLLECTION AND ANALYSIS: Two independent investigators performed the literature search, data extraction, and assessment of methodological quality. The outcomes were expressed with standard mean difference (SMD), HR, or risk ratio (RR) with 95% CI. RESULTS: Thirteen studies involving 112,695 patients were included in this meta-analysis. Among these studies, four studies were cohort studies and nine studies were randomized controlled trials (RCTs). For cohort studies, they were regarded as being of high quality; for RCTs, only one was classified as being at low risk of bias; and the remaining eight studies were at being unclear risk of bias. Compared with other VDRAs, paricalcitol significantly improved the overall survival (HR =0.86, 95% CI: 0.80, 0.92; P<0.001) and reduced the intact parathyroid hormone (iPTH) (SMD =−0.53, 95% CI: −0.90, −0.17; P=0.004). Paricalcitol offered similar effect with other VDRAs in the control of calcium (SMD =0.32, 95% CI: −0.04, 0.67; P=0.078) and phosphorus (SMD =0.06, 95% CI: −0.26, 0.37; P=0.727) levels. However, the serum change in calcium phosphate product was greater in the paricalcitol group than in the other VDRA group (SMD =2.13, 95% CI: 0.19, 4.07; P=0.031). There was no significant difference in the incidence of adverse events between the two groups (RR =1.02, 95% CI: 0.93, 1.12; P=0.674). CONCLUSION: Paricalcitol was crucial in reducing the mortality in patients undergoing hemodialysis. Moreover, both paricalcitol and other VDRAs were effective in control of the serum iPTH, calcium, and phosphorus levels. Given the potential limitations in this study, more prospective large-scale, well-conducted RCTs are needed to confirm these findings. Dove Medical Press 2019-03-28 /pmc/articles/PMC6445244/ /pubmed/30992658 http://dx.doi.org/10.2147/DDDT.S176257 Text en © 2019 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed
spellingShingle Original Research
Liu, Yang
Liu, Ling-Yun
Jia, Ye
Wu, Mei-Yan
Sun, Yan-Yan
Ma, Fu-Zhe
Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
title Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
title_full Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
title_fullStr Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
title_full_unstemmed Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
title_short Efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
title_sort efficacy and safety of paricalcitol in patients undergoing hemodialysis: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445244/
https://www.ncbi.nlm.nih.gov/pubmed/30992658
http://dx.doi.org/10.2147/DDDT.S176257
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