Evidence map›Paper›PMID 42389641›Full record

ArticleFrontiers in cardiovascular medicine2026

The association of remnant cholesterol inflammatory index with the risk of major adverse cardiovascular events in patients with angina undergoing percutaneous coronary intervention: a retrospective study.

Yazhao Sun, Xiao Yu, Chunlan Bai, Dongsheng Liu, Wenrui Xiong

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Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Yazhao SunDepartment of Cardiology, Cangzhou People's Hospital, Cangzhou, Hebei, China.
Xiao YuDepartment of Neurology Intervention, Cangzhou People's Hospital, Cangzhou, Hebei, China.
Chunlan BaiDepartment of Cardiology, Cangzhou People's Hospital, Cangzhou, Hebei, China.
Dongsheng LiuDepartment of Cardiology, Cangzhou People's Hospital, Cangzhou, Hebei, China.
Wenrui XiongDepartment of Scientific Research, Cangzhou People's Hospital, Cangzhou, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The remnant cholesterol-inflammation index (RCII), which combines remnant cholesterol (RC) and high-sensitivity C-reactive protein (hs-CRP), reflects both metabolic and inflammatory risks. This study aims to evaluate the association between RCII and the risk of major adverse cardiovascular events (MACE) in patients with angina undergoing percutaneous coronary intervention (PCI). Methods: The association between baseline RCII and MACE risk was evaluated using multivariable Cox regression, restricted cubic spline (RCS) analysis, and time-dependent receiver operating characteristic (ROC) curves. Results: A total of 2,171 angina patients undergoing PCI were included (mean age 65.32 ± 6.85 years, 61.4% male), with a median follow-up of 36 months, during which 363 MACE events (16.7%) occurred. In the fully adjusted Cox model, each standard deviation increase in RCII was associated with a 5% higher MACE risk (HR = 1.05, 95%CI: 1.04-1.07); compared with the lowest tertile, the HRs for T2 and T3 were 2.87 (95%CI: 2.03-4.04) and 4.42 (95%CI: 3.09-6.32). Subgroup analysis revealed that RCII was significantly associated with MACE risk across different age groups (<65 years and ≥65 years), sex, smoking status, and the presence of coronary artery disease (CAD) history, diabetes, and hypertension, with no significant interactions observed between subgroups. RCS analysis revealed a non-linear positive association ( Conclusion: Baseline RCII may be a potential clinical biomarker for assessing the risk of new-onset MACE in patients with angina undergoing PCI.

Indexed as

coronary artery diseasehigh-sensitivity c-reactive proteinmajor adverse cardiovascular eventspercutaneous coronary interventionremnant cholesterol-inflammation index

Identifiers

PMID42389641
PMCPMC13318779

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