Are elevated levels of IL-6 or hs-CRP associated with adverse clinical outcomes in patients with stable coronary heart disease?
IL-6, but not hs-CRP, is independently associated with major adverse cardiovascular events and mortality in patients with stable coronary heart disease, suggesting it may reflect a key pathophysiological process.
Background Evaluation of cardiovascular prognosis in patients with stable coronary heart disease is based on clinical characteristics and biomarkers indicating dysglycemia, dyslipidemia, renal dysfunction, and possibly cardiac dysfunction. Inflammation plays a key role in atherosclerosis, but the association between inflammatory biomarkers and clinical outcomes is less studied in this population. Methods and Results Overall, 15 828 patients with coronary heart disease in the STABILITY (Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy) trial were randomized to treatment with darapladib or placebo and observed for a median of 3.7 years. In 14 611 patients, levels of interleukin‐6 ( IL ‐6) and high‐sensitivity C‐reactive protein were measured in plasma samples: median levels were 2.1 (interquartile range, 1.4–3.2) ng/L and 1.3 (interquartile range, 0.6–3.1) mg/L, respectively. Associations between continuous levels or quartile groups and adjudicated outcomes were evaluated by spline graphs and Cox regression adjusted for clinical factors and cardiovascular biomarkers. IL ‐6 was associated with increased risk of major adverse cardiovascular events (quartile 4 versus quartile 1 hazard ratio HR , 1.60; 95% confidence interval CI, 1.30–1.97; P <0.0001); cardiovascular death ( HR , 2.15; 95% CI, 1.53–3.04; P <0.0001); myocardial infarction ( HR , 1.53; 95% CI, 1.14–2.04; P <0.05); all‐cause mortality ( HR , 2.11; 95% CI, 1.62–2.76; P <0.0001); and risk of hospitalization for heart failure ( HR , 2.28; 95% CI, 1.34–3.89; P <0.001). Cancer death was doubled in the highest IL ‐6 quartile group ( HR , 2.34; 95% CI, 1.20–4.53; P <0.05). High‐sensitivity C‐reactive protein was associated with both cardiovascular and non‐cardiovascular events in the unadjusted model, but these did not remain after multivariable adjustments. Conclusions IL ‐6, an upstream inflammatory marker, was independently associated with the risk of major adverse cardiovascular events, cardiovascular and all‐cause mortality, myocardial infarction, heart failure, and cancer mortality in patients with stable coronary heart disease. IL‐6 might reflect a pathophysiological process involved in the development of these events. Clinical Trial Registration URL : http://www.clinicaltrials.gov . Unique identifier: NCT 00799903.
Held et al. (2017) studied this question.