4.7 Article

The Biomarker GlycA Is Associated with Chronic Inflammation and Predicts Long-Term Risk of Severe Infection

Journal

CELL SYSTEMS
Volume 1, Issue 4, Pages 293-301

Publisher

CELL PRESS
DOI: 10.1016/j.cels.2015.09.007

Keywords

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Funding

  1. National Health and Medical Research Council of Australia (NHMRC) [APP1062227]
  2. NHMRC
  3. Australian Heart Foundation Career Development Fellowship [1061435]
  4. Victorian Life Sciences Computation Initiative (VLSCI)
  5. University of Oulu
  6. Sigrid Juselius Foundation
  7. Academy of Finland [141136, 139, 635]
  8. Yrjo Jahnsson Foundation
  9. Emil Aaltonen Foundation
  10. Finnish Diabetes Research Foundation
  11. Finnish Foundation for Cardiovascular Research
  12. Oulu University Central Hospital Medical Fund
  13. Helsinki University Central Hospital Medical Fund
  14. Kuopio University Central Hospital Medical Fund
  15. Tampere University Central Hospital Medical Fund
  16. Turku University Central Hospital Medical Fund
  17. Paavo Nurmi Foundation
  18. Juho Vainio Foundation
  19. Finnish Cultural Foundation
  20. Finnish Funding Agency for Technology and Innovation
  21. Paulo Foundation
  22. Maud Kuistila Foundation
  23. Finnish Medical Foundation
  24. British Heart Foundation
  25. Wellcome Trust
  26. Medical Research Council, UK
  27. Academy of Finland (AKA) [141136, 141136] Funding Source: Academy of Finland (AKA)
  28. Novo Nordisk Fonden [NNF15OC0015998] Funding Source: researchfish

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The biomarker glycoprotein acetylation (GlycA) has been shown to predict risk of cardiovascular disease and all-cause mortality. Here, we characterize biological processes associated with GlycA by leveraging population-based omics data and health records from > 10,000 individuals. Our analyses show that GlycA levels are chronic within individuals for up to a decade. In apparently healthy individuals, elevated GlycA corresponded to elevation of myriad inflammatory cytokines, as well as a gene coexpression network indicative of increased neutrophil activity, suggesting that individuals with high GlycA may be in a state of chronic inflammatory response. Accordingly, analysis of infection-related hospitalization and death records showed that increased GlycA increased long-term risk of severe non-localized and respiratory infections, particularly septicaemia and pneumonia. In total, our work demonstrates that GlycA is a biomarker for chronic inflammation, neutrophil activity, and risk of future severe infection. It also illustrates the utility of leveraging multilayered omics data and health records to elucidate the molecular and cellular processes associated with biomarkers.

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