Key result
Highest Remnant Cholesterol Inflammation Index linked to ~2.1-fold higher 30-day post-AMI MACCE risk.
Why the study?
Despite treatment, residual cardiovascular and cerebrovascular risk persists after AMI. Although the Remnant Cholesterol Inflammation Index (RCII) combines residual cholesterol and hsCRP to reflect lipid and inflammatory burdens, its prognostic value in the acute phase remained unclear.
Does the Remnant Cholesterol Inflammation Index (RCII) predict 30-day major adverse cardiovascular and cerebrovascular events (MACCE) in patients with acute myocardial infarction?
Observational (n=3,280)
No
Does the Remnant Cholesterol Inflammation Index (RCII) predict 30-day major adverse cardiovascular and cerebrovascular events (MACCE) in patients with acute myocardial infarction?
The Remnant Cholesterol Inflammation Index (RCII) exhibits a U-shaped association with 30-day major adverse cardiovascular and cerebrovascular events after acute myocardial infarction, suggesting its potential utility as an integrated lipid-inflammatory biomarker for early risk stratification.
Answers are grounded in this paper and cite their sources.
May support integrated remnant cholesterol-inflammation assessment post-AMI; leaves open prospective validation before clinical use.
Background Despite treatment, residual cardiovascular and cerebrovascular risk persists post-acute myocardial infarction (AMI). The Remnant Cholesterol Inflammation Index (RCII), combining residual cholesterol and hsCRP, reflects lipid and inflammatory burdens; however, its prognostic value in the acute phase remains unclear. This study evaluated RCII for predicting 30-day major adverse cardiovascular and cerebrovascular events (MACCE). Methods A single-centre, retrospective study enrolled 3,280 AMI patients. The primary endpoint was a composite of all-cause mortality, recurrent myocardial infarction and non-fatal stroke within 30 days. Covariates were selected via Boruta and LASSO algorithms. Restricted cubic spline (RCS) and segmented Cox regression analysed the dose-response relationship and threshold effects between lnRCII and outcomes. Subgroup and sensitivity analyses were performed. Results lnRCII showed a U-shaped association with 30-day MACCE risk (inflection point: 1.83). Compared to the middle quartile (Q2), patients in Q1, Q3, and Q4 had significantly higher risks (80%, 102%, and 109%, respectively). The association differed by hypertension status ( p for interaction = 0.039), with sensitivity analyses confirming robustness. Conclusion This study suggests that RCII may be an independent predictor of 30-day MACCE post-AMI, with both high and low levels correlating with increased risk. These findings should be interpreted as hypothesis-generating. RCII may serve as an integrated biomarker reflecting both lipid and inflammatory burdens for early risk stratification. Trial registration The study was approved by the Ethics Committee of the First Hospital of Hebei Medical University (approval no. Y277) and was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki. The need for informed consent was waived by the board.
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Chen et al. (2026) conducted an observational in Acute myocardial infarction (n=3,280). Remnant Cholesterol Inflammation Index (lnRCII, highest quartile Q4: >3.72) vs. Middle quartile of lnRCII (Q2: 1.37–2.53) was evaluated on Major adverse cardiovascular and cerebrovascular events (MACCE: composite of all-cause mortality, recurrent myocardial infarction, and non-fatal stroke) within 30 days (HR 2.09, 95% CI 1.34-3.27, p=0.001). Remnant Cholesterol Inflammation Index (lnRCII) showed a U-shaped association with 30-day MACCE post-AMI, with higher risk in Q4 (HR 2.09) and Q1 (HR 1.80) versus Q2.
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