Abstract

Background: Previous studies have demonstrated an association between hyperuricemia and cardiovascular disease (CVD). The Framingham study confirmed that patients with high atherosclerotic risks (HARs) had worse prognoses. However, after adjusting for confounding factors, the association between serum uric acid (SUA) and all-cause mortality and cardiovascular mortality remains unclear, especially for HAR patients.Objective: The aim of this study was to reveal the relationship of SUA with all-cause and cardiovascular mortality in HAR patients.Methods: This multicenter cohort study enrolled 3,047 participants, and the follow-up was 68.85 ± 11.37 months. Factors related to cardiovascular and all-cause mortality were tested by multivariate Cox regression analysis. Restricted cubic splines (RCSs) with knots were used to explore the shape of the dose–response relationship with SUA and the hazard ratio (HR) of all-cause and CVD mortality. SUA transformed by RCS was added to the Cox regression model as an independent variable, and all-cause and CVD mortality scores were calculated. Survival receiver operating characteristic curves were produced using a regression model predicting the score.Results: SUA demonstrated a “U-shaped” relationship with all-cause and cardiovascular mortality. SUA predicted all-cause and CVD mortality, with cutoff values of values of >370.5 μmol/L for males and >327.65 μmol/L for females and <180.5 μmol/L for males and <165.7 μmol/L for females, respectively. The survival ROC curve indicated that SUA is able to predict all-cause and CVD mortality, with areas under the curve of 0.702 and 0.711, respectively. The HRs of all-cause mortality (male and female) with hyperuricemia and hypouricemia were 2.08 and 2.01 and 2.04 and 1.98, respectively, and the HRs of CVD mortality (male and female) were 2.09 and 1.79, and 2.02 and 1.89, respectively.Conclusion: Abnormal SUA levels were significant and independent risk factors for all-cause and CVD mortality. Hyperuricemia and hypouricemia increased mortality in both males and females. Routine SUA evaluation and intensive management are needed for HAR patients.Clinical Trial Registration: www.ClinicalTrials.gov, identifier: NCT03616769.

Highlights

  • Previous studies have demonstrated an association between hyperuricemia and cardiovascular disease (CVD)

  • Our research showed hyperuricemia and hypouricemia prevalences of 18.1 and 16.7%, respectively, and the average serum uric acid (SUA) for the entire cohort was 322.65 ± 33.12 μmol/L

  • Regarding subjects with high atherosclerotic risk (HAR), there was no significant difference for ischemic stroke, myocardial infarction (MI) history, coronary artery bypass grafting (CABG) history, percutaneous coronary angioplasty (PTCA) history, diabetes mellitus (DM), dyslipidemia, and smoking

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Summary

Introduction

Previous studies have demonstrated an association between hyperuricemia and cardiovascular disease (CVD). The Framingham study confirmed that patients with high atherosclerotic risks (HARs) had worse prognoses. After adjusting for confounding factors, the association between serum uric acid (SUA) and all-cause mortality and cardiovascular mortality remains unclear, especially for HAR patients. Previous studies in humans have demonstrated an association between hyperuricemia, arterial stiffness, and endothelial dysfunction [1], and the serum uric acid (SUA) level has been suggested to be an important modulator of the inflammatory process [2]. The Framingham Heart Study found that patients with high atherosclerotic risk (HAR) have worse CVD prognosis [12–14]. The aim of this research was to explore relationships among SUA levels, all-cause mortality, and cardiovascular mortality in HAR patients

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