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Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis

BACKGROUND: As the C-terminal section of vasopressin precursor, copeptin has been recently suggested as a new prognostic biomarker after heart failure (HF). Thus, the aim of this study was to evaluate the prognostic value of plasma copeptin level with all-cause mortality in patients with HF. METHODS...

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Autores principales: Zhang, Peng, Wu, Xiaomei, Li, Guangxiao, Sun, Hao, Shi, Jingpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221547/
https://www.ncbi.nlm.nih.gov/pubmed/28115852
http://dx.doi.org/10.2147/TCRM.S124689
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author Zhang, Peng
Wu, Xiaomei
Li, Guangxiao
Sun, Hao
Shi, Jingpu
author_facet Zhang, Peng
Wu, Xiaomei
Li, Guangxiao
Sun, Hao
Shi, Jingpu
author_sort Zhang, Peng
collection PubMed
description BACKGROUND: As the C-terminal section of vasopressin precursor, copeptin has been recently suggested as a new prognostic biomarker after heart failure (HF). Thus, the aim of this study was to evaluate the prognostic value of plasma copeptin level with all-cause mortality in patients with HF. METHODS: Comprehensive strategies were used to search relevant studies from electronic databases. Pooled hazard ratios (HRs) and standardized mean differences (SMDs) together with their 95% confidence intervals (CIs) were calculated. Subgroup analysis and sensitivity analysis were performed to find the potential sources of heterogeneity. RESULTS: A total of 5,989 participants from 17 prospective studies were included in this meta-analysis. A significant association was observed between circulating copeptin levels and risk of all-cause mortality in patients with HF (categorical copeptin: HR =1.69, 95% CI =1.42–2.01; per unit copeptin: HR =1.03, 95% CI =1.00–1.07; log unit copeptin: HR =3.26, 95% CI =0.95–11.25). Pooled SMD showed that copeptin levels were significantly higher in patients with HF who died during the follow-up period than in survivors (SMD =1.19, 95% CI =0.81–1.57). Subgroup analyses also confirmed this significant association, while sensitivity analyses indicated that the overall results were stable. CONCLUSION: This study demonstrated that circulating copeptin seemed to be a novel biomarker to provide better prediction of all-cause mortality in patients with HF.
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spelling pubmed-52215472017-01-23 Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis Zhang, Peng Wu, Xiaomei Li, Guangxiao Sun, Hao Shi, Jingpu Ther Clin Risk Manag Original Research BACKGROUND: As the C-terminal section of vasopressin precursor, copeptin has been recently suggested as a new prognostic biomarker after heart failure (HF). Thus, the aim of this study was to evaluate the prognostic value of plasma copeptin level with all-cause mortality in patients with HF. METHODS: Comprehensive strategies were used to search relevant studies from electronic databases. Pooled hazard ratios (HRs) and standardized mean differences (SMDs) together with their 95% confidence intervals (CIs) were calculated. Subgroup analysis and sensitivity analysis were performed to find the potential sources of heterogeneity. RESULTS: A total of 5,989 participants from 17 prospective studies were included in this meta-analysis. A significant association was observed between circulating copeptin levels and risk of all-cause mortality in patients with HF (categorical copeptin: HR =1.69, 95% CI =1.42–2.01; per unit copeptin: HR =1.03, 95% CI =1.00–1.07; log unit copeptin: HR =3.26, 95% CI =0.95–11.25). Pooled SMD showed that copeptin levels were significantly higher in patients with HF who died during the follow-up period than in survivors (SMD =1.19, 95% CI =0.81–1.57). Subgroup analyses also confirmed this significant association, while sensitivity analyses indicated that the overall results were stable. CONCLUSION: This study demonstrated that circulating copeptin seemed to be a novel biomarker to provide better prediction of all-cause mortality in patients with HF. Dove Medical Press 2017-01-05 /pmc/articles/PMC5221547/ /pubmed/28115852 http://dx.doi.org/10.2147/TCRM.S124689 Text en © 2017 Zhang 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
Zhang, Peng
Wu, Xiaomei
Li, Guangxiao
Sun, Hao
Shi, Jingpu
Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
title Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
title_full Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
title_fullStr Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
title_full_unstemmed Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
title_short Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
title_sort prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221547/
https://www.ncbi.nlm.nih.gov/pubmed/28115852
http://dx.doi.org/10.2147/TCRM.S124689
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