Why the study?
Predicting MACEs offers significant clinical benefits in coronary artery disease, prompting an evaluation of the prognostic value of plasma von Willebrand factor levels.
Do elevated plasma von Willebrand factor levels predict major adverse cardiovascular events in patients with coronary artery disease?
Do elevated plasma von Willebrand factor levels predict major adverse cardiovascular events in patients with coronary artery disease?
Elevated plasma von Willebrand factor levels at 24 and 48 hours after admission may serve as an independent prognostic biomarker for major adverse cardiovascular events in patients with coronary artery disease.
Answers are grounded in this paper and cite their sources.
Plasma vWF levels were associated with MACE risk in CAD; leaves open added prognostic value beyond standard scores in prospective cohorts.
BACKGROUND: Prediction of major adverse cardiovascular events (MACEs) may offer great benefits for patients with coronary artery disease (CAD). Von Willebrand factor (vWF) is stored in endothelial cells and released into blood plasma upon vascular dysfunction. This meta-analysis was performed to evaluate the prognostic value of plasma vWF levels in CAD patients with MACEs. METHODS: A total of 15 studies were included in this meta-analysis through the search in PubMed, Embase and CNKI. Data were collected from 960 patients who had MACEs after CAD and 3224 controls nested without the adverse events. The standard mean difference (SMD) and 95% confidence intervals (95% CI) were calculated using random-effects model. RESULTS: The plasma vWF levels examined at 24 h and 48 h after admission were significantly higher in CAD patients with MACEs than those without. The pooled SMD among the MACEs group and the non-MACEs group was 0.55 (95% CI = 0.30-0.80, P < 0.0001) and 0.70 (95% CI = 0.27-1.13, P = 0.001), respectively. However, no significant difference was found in plasma vWF levels on admission between the two groups. CONCLUSION: Plasma vWF level in CAD patients examined at 24 h and 48 h after admission might be an independent prognostic factor for MACE.
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Fan et al. (2020) studied this question.
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