Key result
Elevated admission hsCRP is linked to ~9% higher risk of death or reinfarction, driven by NSTEMI.
Why the study?
The inflammatory component of atherosclerosis and its correlation with acute coronary syndrome prognosis, specifically the role of hsCRP, required further investigation.
Does admission hsCRP level predict the composite of cardiac death and myocardial reinfarction in patients with acute coronary syndrome?
Cohort (n=151)
Does admission hsCRP level predict the composite of cardiac death and myocardial reinfarction in patients with acute coronary syndrome?
Hazard Ratio: 1.091 (95% CI 1.014–1.174)
p-value: p=0.019
Admission hsCRP provides additional prognostic value beyond the GRACE risk score for predicting cardiac death and reinfarction in patients with non-STEMI, but not STEMI.
May refine non-STEMI prognostication beyond GRACE; hypothesis-generating and should not yet change practice in ACS.
INTRODUCTION: Atherosclerosis is an active process and the inflammatory component appears to be particularly correlated with the development of acute coronary syndromes (ACS). C-reactive protein (CRP) is an acute phase protein that appears in the circulation in response to inflammatory cytokines. The present study investigated the association between high-sensitivity C-reactive protein (hsCRP) on admission and follow-up prognosis after an ACS. METHODS: We included 151 consecutive patients admitted to the coronary care unit with a diagnosis of ACS (47% ST-segment elevation myocardial infarction [STEMI]). The primary endpoint was the combination of cardiac death and myocardial reinfarction during the follow-up period (median 19.8 months, interquartile range 16.3-23.7 months). RESULTS: The occurrence of follow-up events was significantly related to admission hsCRP level, which was an excellent predictor of cardiac death and reinfarction during follow-up (HR 1.091, 95% CI 1.014-1.174; p=0.019). Stratifying the population based on type of ACS, adjusted by variables associated with cardiac events in univariate analysis (hsCRP, diabetes, depressed ejection fraction and GRACE risk score), hsCRP proved to be an independent predictor of follow-up outcomes only in non-STEMI patients (HR 1.217, 95% CI: 1.093-1.356, p<0.001), not in STEMI patients. The best cutoff level of hsCRP to predict follow-up outcomes was 1.1mg/dl, with sensitivity of 77.8% and specificity of 63.2%. CONCLUSION: Although the GRACE risk score is routinely used for stratification of patients with ACS, assessment of hsCRP may provide additional prognostic value in the follow-up of non-STEMI patients.
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Raposeiras‐Roubín et al. (2013) conducted a cohort in Acute coronary syndrome (n=151). High-sensitivity C-reactive protein (hsCRP) was evaluated on Combination of cardiac death and myocardial reinfarction (HR 1.091, 95% CI 1.014-1.174, p=0.019). Admission high-sensitivity C-reactive protein predicted cardiac death and reinfarction overall (HR 1.091; 95% CI 1.014-1.174; p=0.019), but was an independent predictor only in non-STEMI patients.
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