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Published on: January 28, 2020
Mortality risk prediction of high-sensitivity C-reactive protein in suspected acute coronary syndrome: A cohort study
Amit Kaura1,2, Adam Hartley1,2, Vasileios Panoulas1,2
1National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Mildly elevated high-sensitivity C-reactive protein (hsCRP) levels up to 15 mg/L predict mortality risk in suspected acute coronary syndrome (ACS) patients. This finding is independent of troponin and suggests hsCRP
Area of Science:
- Cardiology
- Biomarkers
- Inflammation
Background:
- Limited evidence exists on high-sensitivity C-reactive protein (hsCRP) as a biomarker for advanced cardiovascular therapies.
- The prognostic value of mildly elevated hsCRP beyond troponin in acute coronary syndrome (ACS) is largely unknown.
- This study investigates hsCRP's association with mortality risk in suspected ACS patients.
Purpose of the Study:
- To evaluate if mildly elevated hsCRP (up to 15 mg/L) is associated with mortality risk.
- To determine if this association is independent of troponin levels.
- To explore hsCRP's potential as a prognostic marker in ACS.
Main Methods:
- Retrospective cohort study of 102,337 patients with suspected ACS (2010-2017).
- Patients categorized into four hsCRP groups (<2, 2-4.9, 5-9.9, 10-15 mg/L).
- Multivariable Cox regression analysis assessed 3-year all-cause mortality, adjusted for clinical factors and troponin.
Main Results:
- A graded relationship observed between hsCRP levels and mortality risk at baseline and 3 years.
- Hazard ratios for mortality increased with hsCRP levels (e.g., 2.00 for 10-15 mg/L group).
- This association remained significant and independent of troponin levels in suspected ACS patients.
Conclusions:
- Mildly elevated hsCRP (up to 15 mg/L) is a clinically meaningful prognostic marker in suspected ACS.
- hsCRP may aid in identifying patients who could benefit from novel anti-inflammatory treatments.
- Real-world data support hsCRP's utility beyond troponin for risk stratification in ACS.
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