4.5 Article

Interleukin-6 and C-reactive protein and risk for death and cardiovascular events in patients with atrial fibrillation

Journal

AMERICAN HEART JOURNAL
Volume 170, Issue 6, Pages 1151-1160

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.ahj.2015.09.018

Keywords

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Funding

  1. Boehringer-Ingelheim
  2. Bristol-Myers Squibb/Pfizer
  3. Aryx Therapeutics
  4. Sanofi-Aventis
  5. Portola Pharmaceuticals
  6. Eli Lilly
  7. Daiichi Sankyo
  8. AstraZeneca
  9. the Medicine Company
  10. GlaxoSmithKline
  11. Merck Co
  12. Abbott
  13. Athera Biotechnologies
  14. Regado Biosciences
  15. Bayer
  16. Bristol-Myers Squibb
  17. Pfizer

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Background Inflammation has been associated with cardiovascular disease and the burden of atrial fibrillation (AF). In this study we evaluate inflammatory biomarkers and future cardiovascular events in AF patients in the RE-LY study. Methods Interleukin-6 (IL-6), C-reactive protein (CRP) (n = 6,187), and fibrinogen (n = 4,893) were analyzed at randomization; outcomes were evaluated by Cox models and C-statistics. Results Adjusted for clinical risk factors IL-6 was independently associated with stroke or systemic embolism (P =.0041), major bleedings (P =.0001), vascular death (P<.0001), and a composite thromboembolic outcome (ischemic stroke, systemic embolism, myocardial infarction, pulmonary embolism and vascular death) (P<.0001). CRP was independently related to myocardial infarction (P =.0047), vascular death (P =.0004), and the composite thromboembolic outcome (P =.0001). When further adjusted for cardiac (troponin andN-terminal fragment B-type natriuretic peptide [NT-proBNP]) and renal (cystatin-C) biomarkers on top of clinical risk factors IL-6 remained significantly related to vascular death (P<.0001), major bleeding (P<.0170) and the composite thromboembolic outcome (P<.0001), and CRP to myocardial infarction (.0104). Fibrinogen was not associated with any outcome. C-index for stroke or systemic embolism increased from 0.615 to 0.642 (P =.0017) when adding IL-6 to the clinically used CHA(2)DS(2)-VASc risk score with net reclassification improvement of 28%. Conclusion In patients with AF, IL-6 is related to higher risk of stroke and major bleeding, and both markers are related to higher risk of vascular death and the composite of thromboembolic events independent of clinical risk factors. Adjustment for cardiovascular biomarkers attenuated the prognostic value, although IL-6 remained related to mortality, the composite of thromboembolic events, and major bleeding, and CRP to myocardial infarction.

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