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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.
Background:
The incremental prognostic value of plasma levels of C-reactive protein (CRP) in relation to GRACE score has not been established in patients with acute coronary syndrome (ACS) with non-ST segment elevation.
Objective:
To test the hypothesis that CRP measurements at admission increases the prognostic value of GRACE score in patients with ACS.
Methods:
A total of 290 subjects, consecutively admitted for ACS, with plasma material obtained upon admission CRP measurement using a high-sensitivity method (nephelometry) were studied. Cardiovascular outcomes during hospitalization were defined by the combination of death, nonfatal myocardial infarction or nonfatal refractory angina.
Results:
The incidence of cardiovascular events during hospitalization was 15% (18 deaths, 11 myocardial infarctions, 13 angina episodes) with CRP showing C-statistics of 0.60 (95% CI = 0.51-0.70, p = 0.034) in predicting these outcomes. After adjustment for the GRACE score, elevated CRP (defined as the best cutoff point) tended to be associated with hospital events (OR = 1.89, 95% CI = 0.92 to 3.88, p = 0.08). However, the addition of the variable elevated CRP in the GRACE model did not result in significant increase in C-statistics, which ranged from 0.705 to 0.718 (p = 0.46). Similarly, there was no significant reclassification of risk with the addition of CRP in the predictor model (net reclassification = 5.7 %, p = 0.15).
Conclusion:
Although CRP is associated with hospital outcomes, this inflammatory marker does not increase the prognostic value of the GRACE score.
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