Elevated serum vascular adhesion protein-1 levels (≥1335 ng/mL) were independently associated with a nearly threefold increased risk of major adverse cardiovascular events in heart failure patients.
Cohort (n=165)
No
Do higher circulating VAP-1 levels predict major adverse cardiovascular events and disease progression in patients with heart failure?
356 individuals receiving treatment at Soochow University Hospital, including 165 diagnosed with heart failure
Higher circulating vascular adhesion protein-1 (VAP-1) concentrations
Lower circulating VAP-1 concentrations (e.g., lowest quartile)
Major adverse cardiovascular events (MACE)composite
Elevated circulating VAP-1 levels are independently associated with an increased risk of MACE and heart failure progression, suggesting its potential utility as a prognostic biomarker.
Effect estimate: HR 2.85 (95% CI 1.1-7.36)
Absolute Event Rate: 49.1% vs 30.9%
p-value: p=0.031
Vascular adhesion protein-1 (VAP-1), a multifunctional inflammatory mediator, has been implicated in cardiovascular pathology. Current evidence regarding its prognostic relevance in heart failure (HF) is incomplete. This investigation was designed to evaluate circulating VAP-1 as a biomarker for its association with HF progression susceptibility and its clinical prognostic value for adverse cardiovascular events. This retrospective observational cohort study included 356 individuals receiving treatment at Soochow University Hospital from May 2020 to September 2022, among whom 165 were diagnosed with heart failure. During the baseline evaluation, VAP-1 concentrations in blood serum were measured through ELISA testing. Major adverse cardiovascular events (MACE) were designated the principal study endpoints, with data collected from electronic health records and telephone follow-ups. Analytical methods incorporated multiple regression analysis, nonlinear modeling approaches, and Kaplan-Meier survival probability assessments. Additional analyses examined the association between heart failure progression and VAP-1 levels through multiple regression modeling, ROC curve assessment, and AUC calculations to establish VAP-1’s diagnostic potential for heart failure identification. When accounting for potential confounding factors, higher concentrations of VAP-1 showed a correlation with MACE in patients with HF (Q2 versus Q1: hazard ratios HR = 1.7, 95% confidence intervals CI = 0.71–4.12; Q3 versus Q1: HR = 2.85, 95% CI = 1.1–7.36). These results were further validated through survival probability assessments and non-linear regression modeling. Multiple regression analysis demonstrated that increased VAP-1 levels served as an independent risk factor for heart failure progression (P = 0.0271, HR = 1.0012, 95% CI = 1.0001–1.0022). The study demonstrates a meaningful relationship between heightened VAP-1 concentrations and both the development of heart failure and cardiovascular complications, indicating VAP-1’s possible utility as a diagnostic marker for assessing heart failure risk and clinical outcomes.
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Zhang et al. (Wed,) conducted a cohort in Heart failure (n=165). Vascular adhesion protein-1 (VAP-1) highest tertile vs. Lowest VAP-1 tertile (≤860 ng/mL) was evaluated on Major adverse cardiovascular events (MACE) (HR 2.85, 95% CI 1.1-7.36, p=0.031). Elevated serum vascular adhesion protein-1 levels (≥1335 ng/mL) were independently associated with a nearly threefold increased risk of major adverse cardiovascular events in heart failure patients.
synapsesocial.com/papers/69fd7f86bfa21ec5bbf08030 — DOI: https://doi.org/10.1186/s12872-026-05935-1
You Zhang
Soochow University
Chi Geng
Soochow University
Feng Li
Soochow University
BMC Cardiovascular Disorders
Soochow University
First Affiliated Hospital of Soochow University
Second Affiliated Hospital of Soochow University
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