Abstract

Cardiovascular disease (CVD) is the leading cause of death globally. Risk assessment is crucial for identifying at-risk individuals who require immediate attention as well as to guide the intensity of medical therapy to reduce subsequent risk of CVD. In the past decade, many risk prediction models have been proposed to estimate the risk of developing CVD. However, in patients with a history of CVD, the current models that based on traditional risk factors provide limited power in predicting recurrent cardiovascular events. Several biomarkers from different pathophysiological pathways have been identified to predict cardiovascular events, and the incorporation of biomarkers into risk assessment may contribute to enhance risk stratification in secondary prevention. This review focuses on biomarkers related to cardiovascular and metabolic diseases, including B-type natriuretic peptide, high-sensitivity cardiac troponin I, adiponectin, adipocyte fatty acid-binding protein, heart-type fatty acid-binding protein, lipocalin-2, fibroblast growth factor 19 and 21, retinol-binding protein 4, plasminogen activator inhibitor-1, 25-hydroxyvitamin D, and proprotein convertase subtilisin/kexin type 9, and discusses the potential utility of these biomarkers in cardiovascular risk prediction among patients with CVD. Many of these biomarkers have shown promise in improving risk prediction of CVD. Further research is needed to assess the validity of biomarker and whether the strategy for incorporating biomarker into clinical practice may help to optimize decision-making and therapeutic management.

Highlights

  • Individuals with stable coronary artery disease (CAD) are at higher risk of recurrent cardiovascular event and mortality than the general population

  • Addition of hs-cardiac troponin I (cTnI) improved the area under the receiver operating characteristic (AUC) by 0.03 and an net reclassification index (NRI) of 25% [46]. These findings showed that high-sensitivity cardiac troponin I (hs-cTnI) levels had an additive prognostic value for future cardiovascular outcomes over a conventional model with clinical risk factors

  • Accurate risk stratification tools are important for clinical risk prediction and treatment strategy, for individuals in higher risk groups

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Summary

INTRODUCTION

Individuals with stable coronary artery disease (CAD) are at higher risk of recurrent cardiovascular event and mortality than the general population. Existing prediction models that based on traditional risk factors such as age, gender, diabetes status, blood pressure, cholesterol levels, and smoking status may have limited value to risk stratify patients with stable CAD [2] Circulating biomarkers such as high sensitivity C-reactive protein and cardiac troponin have been playing a crucial role in the diagnosis, risk stratification, and management of patients with several disease conditions including heart failure (HF) and acute coronary syndrome (ACS) [3, 4]. The reviewed biomarkers include: (i) cardiac-related biomarkers [B-type natriuretic peptide (BNP), N-terminal pro-B-type natriuretic peptide (NT-proBNP), and cardiac troponin I (cTnI)]; and (ii) metabolic-related biomarkers [adiponectin, adipocyte fatty acid-binding protein (A-FABP), heart-type fatty acid binding protein (H-FABP), lipocalin-2, fibroblast growth factor (FGF) 19 and 21, retinol-binding protein 4 (RBP4), plasminogen activator inhibitor-1 (PAI-1), 25hydroxyvitamin D, and proprotein convertase subtilisin/kexin type 9 (PCSK9)] These biomarkers are of special interest as they are thought to provide sufficient information for improving cardiovascular risk stratification.

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