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Circulating copeptin level and the clinical prognosis of patients with chronic liver disease

BACKGROUND: The relationship between copeptin and the severity of circulatory dysfunction and systemic stress response in patients with chronic liver disease (CLD) has been established. Nevertheless, the potential of serum copeptin levels to predict the prognosis of CLD patients remains unclear. AIM...

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Autores principales: Tan, Hao-Qian, Zhao, Ming, Huang, Zan, Liu, Yang, Li, Han, Ma, Long-Hui, Liu, Jun-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473920/
https://www.ncbi.nlm.nih.gov/pubmed/37664154
http://dx.doi.org/10.3748/wjg.v29.i31.4797
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author Tan, Hao-Qian
Zhao, Ming
Huang, Zan
Liu, Yang
Li, Han
Ma, Long-Hui
Liu, Jun-Ying
author_facet Tan, Hao-Qian
Zhao, Ming
Huang, Zan
Liu, Yang
Li, Han
Ma, Long-Hui
Liu, Jun-Ying
author_sort Tan, Hao-Qian
collection PubMed
description BACKGROUND: The relationship between copeptin and the severity of circulatory dysfunction and systemic stress response in patients with chronic liver disease (CLD) has been established. Nevertheless, the potential of serum copeptin levels to predict the prognosis of CLD patients remains unclear. AIM: To conduct a systematic review and meta-analysis to investigate the correlation between serum copeptin and transplant-free survival (TFS) in this population. METHODS: To achieve the objective of the meta-analysis, PubMed, Embase, the Cochrane Library, and the Web of Science were searched to identify observational studies with longitudinal follow-up. The Cochrane Q test was utilized to assess between-study heterogeneity, and the I(2) statistic was estimated. Random-effects models were employed to combine the outcomes, taking into account the potential influence of heterogeneity. RESULTS: Ten datasets including 3133 patients were involved. The follow-up durations were 1 to 48 mo (mean: 12.5 mo). Overall, it was shown that a high level of serum copeptin was associated with a poor TFS [risk ratio (RR): 1.82, 95% confidence interval: 1.52-2.19, P < 0.001; I(2) = 0%]. In addition, sensitivity analysis by omitting one dataset at a time showed consistent results (RR: 1.73-2.00, P < 0.05). Finally, subgroup analyses according to study country, study design, patient diagnosis, cutoff of copeptin, follow-up duration, and study quality score also showed similar results (P for subgroup difference all > 0.05). CONCLUSION: Patients with CLD who have high serum copeptin concentrations may be associated with a poor clinical prognosis.
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spelling pubmed-104739202023-09-03 Circulating copeptin level and the clinical prognosis of patients with chronic liver disease Tan, Hao-Qian Zhao, Ming Huang, Zan Liu, Yang Li, Han Ma, Long-Hui Liu, Jun-Ying World J Gastroenterol Meta-Analysis BACKGROUND: The relationship between copeptin and the severity of circulatory dysfunction and systemic stress response in patients with chronic liver disease (CLD) has been established. Nevertheless, the potential of serum copeptin levels to predict the prognosis of CLD patients remains unclear. AIM: To conduct a systematic review and meta-analysis to investigate the correlation between serum copeptin and transplant-free survival (TFS) in this population. METHODS: To achieve the objective of the meta-analysis, PubMed, Embase, the Cochrane Library, and the Web of Science were searched to identify observational studies with longitudinal follow-up. The Cochrane Q test was utilized to assess between-study heterogeneity, and the I(2) statistic was estimated. Random-effects models were employed to combine the outcomes, taking into account the potential influence of heterogeneity. RESULTS: Ten datasets including 3133 patients were involved. The follow-up durations were 1 to 48 mo (mean: 12.5 mo). Overall, it was shown that a high level of serum copeptin was associated with a poor TFS [risk ratio (RR): 1.82, 95% confidence interval: 1.52-2.19, P < 0.001; I(2) = 0%]. In addition, sensitivity analysis by omitting one dataset at a time showed consistent results (RR: 1.73-2.00, P < 0.05). Finally, subgroup analyses according to study country, study design, patient diagnosis, cutoff of copeptin, follow-up duration, and study quality score also showed similar results (P for subgroup difference all > 0.05). CONCLUSION: Patients with CLD who have high serum copeptin concentrations may be associated with a poor clinical prognosis. Baishideng Publishing Group Inc 2023-08-21 2023-08-21 /pmc/articles/PMC10473920/ /pubmed/37664154 http://dx.doi.org/10.3748/wjg.v29.i31.4797 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Meta-Analysis
Tan, Hao-Qian
Zhao, Ming
Huang, Zan
Liu, Yang
Li, Han
Ma, Long-Hui
Liu, Jun-Ying
Circulating copeptin level and the clinical prognosis of patients with chronic liver disease
title Circulating copeptin level and the clinical prognosis of patients with chronic liver disease
title_full Circulating copeptin level and the clinical prognosis of patients with chronic liver disease
title_fullStr Circulating copeptin level and the clinical prognosis of patients with chronic liver disease
title_full_unstemmed Circulating copeptin level and the clinical prognosis of patients with chronic liver disease
title_short Circulating copeptin level and the clinical prognosis of patients with chronic liver disease
title_sort circulating copeptin level and the clinical prognosis of patients with chronic liver disease
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473920/
https://www.ncbi.nlm.nih.gov/pubmed/37664154
http://dx.doi.org/10.3748/wjg.v29.i31.4797
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