Key result
Persistently high hs-CRP after AMI predicts ~49% greater 3-year MACE risk versus persistently low levels.
Why the study?
Residual inflammatory risk after AMI remains an important determinant of long-term outcomes, but the prognostic significance of serial hs-CRP measurements beyond the acute phase remains unclear.
Does 1-year hs-CRP measurement better predict long-term MACE compared to baseline hs-CRP in patients with AMI undergoing PCI?
Cohort (n=16,371)
Yes
Does 1-year hs-CRP measurement better predict long-term MACE compared to baseline hs-CRP in patients with AMI undergoing PCI?
Hazard Ratio: 1.49 (95% CI 1.08–2.06)
p-value: p=0.015
In patients with AMI undergoing PCI, hs-CRP measured at 1 year provides stronger long-term prognostic information for MACE than baseline hs-CRP, highlighting the value of serial inflammatory risk assessment.
Background/Aims: Residual inflammatory risk after acute myocardial infarction (AMI) remains an important determinant of long-term outcomes despite optimal lipid-lowering therapy. The prognostic significance of serial high-sensitivity C-reactive protein (hs-CRP) measurements beyond the acute phase remains unclear. This study compared baseline and 1-year hs-CRP for predicting 3-year major adverse cardiovascular events in patients with AMI undergoing percutaneous coronary intervention.Methods: We analyzed a large prospective AMI registry in which hs-CRP was measured at baseline and 1 year, classifying patients at each time point using a ≥ 2 mg/L threshold. The primary endpoint was 3-year MACE, including cardiovascular death, recurrent myocardial infarction, stroke, repeat revascularization, and stent thrombosis.Results: Among 16,371 patients, 9,618 (58.8%) had elevated hs-CRP at baseline. Of the 5,389 patients with 1-year data, 28.9% had elevated hs-CRP. Baseline hs-CRP predicted MACE within the first year (hazard ratio [HR] 1.38, 95% CI 1.21–1.57); however, this association was no longer significant beyond 1 year. One year hs-CRP independently predicted subsequent 2-year MACE (HR 1.33, 95% CI 1.01–1.77). Patients with persistently high hs-CRP (≥ 2 mg/L at both time points) had the highest 3-year MACE risk (HR 1.49, 95% CI 1.08–2.06, p = 0.015 vs. persistently low group) than patients with recovered, worsening, and persistently low hs-CRP.Conclusions: In patients with AMI, hs-CRP measured at 1-year provides stronger long-term prognostic information than that at baseline beyond 1 year. Routine assessment of hs-CRP may improve risk stratification and guide targeted anti-inflammatory strategies in secondary prevention.
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Seong et al. (2026) conducted a cohort in Acute myocardial infarction (n=16,371). Persistently high hs-CRP (≥ 2 mg/L at baseline and 1 year) vs. Persistently low hs-CRP was evaluated on 3-year MACE, including cardiovascular death, recurrent myocardial infarction, stroke, repeat revascularization, and stent thrombosis (HR 1.49, 95% CI 1.08-2.06, p=0.015). Persistently high hs-CRP (≥ 2 mg/L at baseline and 1 year) after AMI increased the risk of 3-year MACE compared to persistently low hs-CRP (HR 1.49; 95% CI 1.08-2.06; p=0.015).
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