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Prognostic role of copeptin with all-cause mortality after heart failure: a systematic review and meta-analysis
Peng Zhang1, Xiaomei Wu1, Guangxiao Li1
1Department of Clinical Epidemiology, Center of Evidence-Based Medicine, Institute of Cardiovascular Disease, The First Hospital of China Medical University, Shenyang, People's Republic of China.
Insights
Elevated copeptin levels in heart failure (HF) patients are linked to a higher risk of all-cause mortality. This meta-analysis confirms copeptin as a valuable prognostic biomarker for HF.
Area of Science:
- Cardiology
- Biomarkers
- Prognostics
Background:
- Copeptin, a vasopressin precursor fragment, is a potential prognostic biomarker in heart failure (HF).
- Previous studies suggest a link between copeptin levels and HF outcomes.
Purpose of the Study:
- To evaluate the prognostic value of plasma copeptin levels for all-cause mortality in patients with heart failure (HF).
Main Methods:
- A meta-analysis of 17 prospective studies involving 5,989 participants.
- Pooled hazard ratios (HRs) and standardized mean differences (SMDs) were calculated.
- Subgroup and sensitivity analyses were conducted to assess heterogeneity.
Main Results:
- Higher circulating copeptin levels were significantly associated with an increased risk of all-cause mortality in HF patients.
- Copeptin levels were significantly higher in HF patients who died compared to survivors (SMD = 1.19).
- Results remained stable across sensitivity and subgroup analyses.
Conclusions:
- Circulating copeptin is a novel and valuable biomarker for predicting all-cause mortality in patients with heart failure (HF).
- Copeptin may improve risk stratification and patient management in HF.
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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