4.7 Article

High-throughput quantification of circulating metabolites improves prediction of subclinical atherosclerosis

期刊

EUROPEAN HEART JOURNAL
卷 33, 期 18, 页码 2307-2316

出版社

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehs020

关键词

Intimamedia thickness; Risk factors; Lipoproteins; Tyrosine; Metabolomics

资金

  1. Academy of Finland [135973, 121584, 129269, 129429, 250422]
  2. Emil Aaltonen Foundation
  3. Finnish Foundation for Cardiovascular Research
  4. Finnish Cultural Foundation
  5. Instrumentarium Science Foundation
  6. Jenny and Antti Wihuri Foundation
  7. Paulo Foundation
  8. Sigrid Juselius Foundation
  9. Social Insurance Institution of Finland
  10. Tampere University Hospital
  11. Turku University Hospital
  12. Turku University Foundation
  13. Academy of Finland (AKA) [129269, 135973, 250422, 129429, 129269, 250422, 129429, 135973] Funding Source: Academy of Finland (AKA)

向作者/读者索取更多资源

High-throughput metabolite quantification holds promise for cardiovascular risk assessment. Here, we evaluated whether metabolite quantification by nuclear magnetic resonance (NMR) improves prediction of subclinical atherosclerosis in comparison to conventional lipid testing. Circulating lipids, lipoprotein subclasses, and small molecules were assayed by NMR for 1595 individuals aged 2439 years from the population-based Cardiovascular Risk in Young Finns Study. Carotid intimamedia thickness (IMT), a marker of subclinical atherosclerosis, was measured in 2001 and 2007. Baseline conventional risk factors and systemic metabolites were used to predict 6-year incidence of high IMT (epsilon 90th percentile) or plaque. The best prediction of high intimamedia thickness was achieved when total and HDL cholesterol were replaced by NMR-determined LDL cholesterol and medium HDL, docosahexaenoic acid, and tyrosine in prediction models with risk factors from the Framingham risk score. The extended prediction model improved risk stratification beyond established risk factors alone; area under the receiver operating characteristic curve 0.764 vs. 0.737, P 0.02, and net reclassification index 17.6, P 0.0008. Higher docosahexaenoic acid levels were associated with decreased risk for incident high IMT (odds ratio: 0.74; 95 confidence interval: 0.670.98; P 0.007). Tyrosine (1.33; 1.101.60; P 0.003) and glutamine (1.38; 1.131.68; P 0.001) levels were associated with 6-year incident high IMT independent of lipid measures. Furthermore, these amino acids were cross-sectionally associated with carotid IMT and the presence of angiographically ascertained coronary artery disease in independent populations. High-throughput metabolite quantification, with new systemic biomarkers, improved risk stratification for subclinical atherosclerosis in comparison to conventional lipids and could potentially be useful for early cardiovascular risk assessment.

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