6533b827fe1ef96bd1286dbe
RESEARCH PRODUCT
Interleukin-18 Is a Strong Predictor of Cardiovascular Death in Stable and Unstable Angina
Christoph BickelDirk PeetzStefan BlankenbergJürgen MeyerLaurence TiretHans J. RupprechtFrançois Cambiensubject
medicine.medical_specialtyEjection fractionbiologyUnstable anginabusiness.industryC-reactive proteinInterleukinmedicine.diseaseCoronary artery diseaseAnginaEndocrinologyPhysiology (medical)Internal medicinemedicinebiology.proteinCardiologyRisk factorCardiology and Cardiovascular MedicineInterleukin 6businessdescription
Background — Interleukin (IL)-18 plays a central role in orchestrating the cytokine cascade and accelerates atherosclerosis and plaque vulnerability in animal models. However, epidemiological data evaluating the role of IL-18 levels in atherosclerosis are lacking. Methods and Results — In a prospective study of 1229 patients with documented coronary artery disease, we measured baseline serum concentrations of IL-18 and other markers of inflammation. During the follow-up period (median, 3.9 years), 95 patients died of cardiovascular causes. Median serum concentrations of IL-18 were significantly higher among patients who had a fatal cardiovascular event than among those who did not (68.4 versus 58.7 pg/mL; P <0.0001). The hazard risk ratio of future cardiovascular death increased with increasing quartiles of IL-18 (hazard risk ratio, 1.46; 95% CI 1.21 to 1.76; P for trend <0.0001). After adjustment for most potential confounders, including the strong predictor ejection fraction as well as the inflammatory variables IL-6, high-sensitive C-reactive protein, and fibrinogen, this relation remained almost unchanged, such that patients within the highest quartile of IL-18 had a 3.3-fold increase in hazard risk compared with those in the first quartile (95% CI, 1.3 to 8.4, P =0.01). This relation was observed in patients with stable angina and patients with unstable angina at baseline. Conclusions — Serum IL-18 level was identified as a strong independent predictor of death from cardiovascular causes in patients with coronary artery disease regardless of the clinical status at admission. This result strongly supports recent experimental evidence of IL-18–mediated inflammation leading to acceleration and vulnerability of atherosclerotic plaques.
year | journal | country | edition | language |
---|---|---|---|---|
2002-07-02 | Circulation |