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Published on: January 28, 2020
Prognostic value of high-sensitivity C-reactive protein among chronic kidney disease patients undergoing percutaneous
Davis Jones1, Alessandro Spirito2, Samantha Sartori2
1The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Insights
High-sensitivity C-reactive protein (hs-CRP) did not increase major adverse cardiac events (MACE) risk in chronic kidney disease (CKD) patients post-percutaneous coronary intervention (PCI). However, elevated hs-CRP consistently predicted higher mortality in both CKD and non-CKD patients.
Area of Science:
- Cardiology
- Nephrology
- Biomarkers
Background:
- Limited data exists on the prognostic implications of high-sensitivity C-reactive protein (hs-CRP) in patients with chronic kidney disease (CKD) undergoing percutaneous coronary intervention (PCI).
- Inflammation, indicated by hs-CRP, is a known factor in cardiovascular disease progression.
Purpose of the Study:
- To investigate the prognostic value of elevated hs-CRP levels in patients with and without CKD undergoing PCI.
- To determine the association between hs-CRP and major adverse cardiac events (MACE) and all-cause mortality after PCI.
Main Methods:
- A retrospective analysis of 12,410 patients undergoing PCI between January 2012 and December 2019.
- CKD defined as GFR <60 mL/min/1.73m², elevated hs-CRP as >3 mg/L. Excluded were patients with acute MI, acute heart failure, cancer, or on hemodialysis.
- Primary outcome: MACE (all-cause death, MI, target vessel revascularization) at 1-year post-PCI.
Main Results:
- Of 12,410 patients, 3029 (24.4%) had CKD. Elevated hs-CRP was more prevalent in CKD patients (31.8%) vs. non-CKD (25.8%).
- No significant association was found between elevated hs-CRP and MACE at 1-year in CKD (11.0% vs 9.5%) or non-CKD patients (10% vs 8.1%).
- Elevated hs-CRP was independently associated with increased all-cause mortality in both CKD (adj. HR 1.92) and non-CKD patients (adj. HR 3.02).
Conclusions:
- Elevated hs-CRP levels were not associated with an increased risk of 1-year MACE in patients undergoing PCI without acute MI.
- Hs-CRP independently predicted increased all-cause mortality in both CKD and non-CKD patients following PCI.
- No interaction was observed between hs-CRP and CKD status regarding MACE or mortality outcomes.
Background:
Data on the prognostic value of high-sensitivity C-reactive protein (hs-CRP) levels in patients with chronic kidney disease (CKD) undergoing percutaneous coronary intervention (PCI) are limited.
Methods:
Patients undergoing PCI at a tertiary center from January 2012 to December 2019 were included. CKD was defined as a glomerular filtration rate (GFR) <60 mL/min/1.73m2 and elevated hs-CRP was defined as >3 mg/L. Acute myocardial infarction (MI), acute heart failure, neoplastic disease, patients undergoing hemodialysis, or hs-CRP >10 mg/L were exclusion criteria. The primary outcome was major adverse cardiac events (MACE), a composite of all-cause death, MI, and target vessel revascularization at 1-year after PCI.
Results:
Out of 12,410 patients, 3029 (24.4 %) had CKD. Elevated hs-CRP levels were found in 31.8 % of CKD and 25.8 % of no-CKD patients. At 1 year, MACE occurred in 87 (11.0 %) CKD patients with elevated hs-CRP and 163 (9.5 %) with low hs-CRP (adj. HR 1.26, 95 % CI 0.94-1.68); among no-CKD patients, in 200 (10 %) and 470 (8.1 %), respectively (adj. HR 1.21, 95 % CI 1.00-1.45). Hs-CRP was associated with an increased risk of all-cause death in both CKD (Adj. HR 1.92, 95 % CI 1.07-3.44) and no-CKD patients (adj. HR 3.02, 95 % CI 1.74-5.22). There was no interaction between hs-CRP and CKD status.
Conclusions:
Among patients undergoing PCI without acute MI, elevated hs-CRP values were not associated with a higher risk of MACE at 1 year, but with increased mortality hazards consistently in patients with or without CKD.
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