BackgroundThe association between high-sensitivity C-reactive protein and recurrent major
adverse cardiovascular events (MACE) in patients with ST-elevation myocardial
infarction who undergo primary percutaneous coronary intervention remains
controversial.ObjectiveTo investigate the potential association between high-sensitivity C-reactive
protein and an increased risk of MACE such as death, heart failure, reinfarction,
and new revascularization in patients with ST-elevation myocardial infarction
treated with primary percutaneous coronary intervention.MethodsThis prospective cohort study included 300 individuals aged >18 years who were
diagnosed with ST-elevation myocardial infarction and underwent primary
percutaneous coronary intervention at a tertiary health center. An instrument
evaluating clinical variables and the Thrombolysis in Myocardial Infarction (TIMI)
and Global Registry of Acute Coronary Events (GRACE) risk scores was used.
High-sensitivity C-reactive protein was determined by nephelometry. The patients
were followed-up during hospitalization and up to 30 days after infarction for the
occurrence of MACE. Student's t, Mann-Whitney, chi-square, and logistic regression
tests were used for statistical analyses. P values of ≤0.05 were considered
statistically significant.ResultsThe mean age was 59.76 years, and 69.3% of patients were male. No statistically
significant association was observed between high-sensitivity C-reactive protein
and recurrent MACE (p = 0.11). However, high-sensitivity C-reactive protein was
independently associated with 30-day mortality when adjusted for TIMI [odds ratio
(OR), 1.27; 95% confidence interval (CI), 1.07-1.51; p = 0.005] and GRACE (OR,
1.26; 95% CI, 1.06-1.49; p = 0.007) risk scores.ConclusionAlthough high-sensitivity C-reactive protein was not predictive of combined major
cardiovascular events within 30 days after ST-elevation myocardial infarction in
patients who underwent primary angioplasty and stent implantation, it was an
independent predictor of 30-day mortality.