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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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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. |
format | Online Article Text |
id | pubmed-5221547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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