Does C-reactive protein add prognostic value to GRACE score in acute coronary syndromes?

Luis Cláudio Lemos Correia1, Isis Vasconcelos1, Guilherme Garcia1

  • 1Escola Bahiana de Medicina e Saúde Pública, Salvador, BA, Brasil.

Insights

Plasma C-reactive protein (CRP) levels are associated with hospital outcomes in acute coronary syndrome (ACS) patients. However, CRP does not improve the prognostic accuracy of the GRACE score for predicting these events.

Area of Science:

  • Cardiology
  • Biomarkers
  • Clinical Prognostics

Background:

  • The prognostic utility of C-reactive protein (CRP) in acute coronary syndrome (ACS) with non-ST segment elevation, relative to the GRACE score, remains unclear.
  • Assessing novel biomarkers alongside established risk scores is crucial for refining patient management.

Purpose of the Study:

  • To evaluate whether plasma CRP levels at admission enhance the prognostic value of the GRACE score in ACS patients.
  • To determine if CRP provides incremental predictive information beyond the GRACE score for in-hospital cardiovascular events.

Main Methods:

  • A cohort of 290 ACS patients had plasma CRP measured using high-sensitivity nephelometry upon admission.
  • Cardiovascular outcomes included in-hospital death, nonfatal myocardial infarction, or refractory angina.
  • Statistical analyses assessed CRP's predictive performance and its incremental value when added to the GRACE score.

Main Results:

  • The incidence of in-hospital cardiovascular events was 15%.
  • Elevated CRP showed a trend towards association with hospital events after GRACE score adjustment (OR = 1.89, p = 0.08).
  • Adding CRP to the GRACE model did not significantly improve C-statistics (0.705 to 0.718, p = 0.46) or risk reclassification (5.7%, p = 0.15).

Conclusions:

  • While C-reactive protein (CRP) is linked to adverse hospital outcomes in ACS patients, it does not augment the prognostic capabilities of the GRACE score.
  • The GRACE score alone appears sufficient for risk stratification in this patient population, without added benefit from CRP.
Abstract

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