C-reactive protein, diastolic dysfunction, and risk of heart failure in patients with coronary disease: Heart and

Eric S Williams1, Sanjiv J Shah, Sadia Ali

  • 1San Francisco Veterans Affairs Medical Center and the University of California, San Francisco, CA, USA. eric.williams@ucsf.edu

Insights

Elevated high-sensitivity C-reactive protein (CRP) predicts heart failure (HF) hospitalizations in coronary heart disease (CHD) patients. This link appears to be explained by abnormal diastolic function, not just underlying CHD.

Area of Science:

  • Cardiology
  • Inflammation Research
  • Clinical Medicine

Background:

  • High-sensitivity C-reactive protein (CRP) is a known predictor of coronary heart disease (CHD).
  • Recent studies suggest CRP also predicts incident heart failure (HF).
  • The relationship between inflammation and HF, mediated by left ventricular dysfunction or CHD, remains unclear.

Purpose of the Study:

  • To investigate whether inflammation, indicated by CRP, predicts heart failure hospitalizations in patients with established CHD.
  • To determine if this association is explained by baseline left ventricular dysfunction or underlying coronary heart disease.

Main Methods:

  • Serum CRP levels were measured in 985 outpatients with established CHD.
  • Participants were followed for 3 years for hospitalisation due to HF.
  • Multivariate analysis adjusted for traditional risk factors, CHD severity, myocardial infarction (MI), and diastolic dysfunction.

Main Results:

  • 15% of patients with elevated CRP (>3 mg/L) were hospitalised for HF versus 7% with lower CRP levels.
  • Elevated CRP was associated with HF hospitalization after adjusting for traditional risk factors, CHD severity, and interim MI (aHR 2.1).
  • This association was no longer significant after adjusting for diastolic dysfunction (aHR 1.6).

Conclusions:

  • Elevated CRP levels predict heart failure hospitalisation in stable CHD outpatients, independent of other factors.
  • The predictive value of CRP for HF in this cohort is at least partly explained by the presence of diastolic dysfunction.
  • Inflammation, as measured by CRP, may contribute to HF development through impaired cardiac function.
Abstract

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