Evidence map›Paper›PMID 40830803›Full record

ArticleEuropean journal of medical research2025

Influence of systemic immunoinflammatory index on major adverse cardiovascular events in patients with coronary heart disease with heart failure as assessed by propensity score matching.

ZhiRong Ren, JinWen Liu

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Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

ZhiRong RenDepartment of Internal Medicine I, Chinese People's Armed Police Force, Shanxi Provincial Corps Hospital, Taiyuan City, 030006, Shanxi Province, China.
JinWen LiuDepartment of Interventional Treatment Room, Shanxi Bethune Hospital (Shanxi Academy of Medical Sciences; Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University), No. 99, Longcheng Street, Taiyuan City, 030032, Shanxi Province, China. liu_jinwen98@outlook.com.

Funding

National Natural Science Foundation of China No. 82170398
6 · The paper itself

Abstract

objectivesThis research aimed to evaluate the influence of the systemic immunoinflammatory index (SII) on the development of major adverse cardiovascular events (MACE) in individuals with coronary heart disease (CHD) and heart failure (HF), as determined by propensity score matching (PSM).

methodsThe 218 patients with CHD and HF were divided into the MACE group and the non-MACE group. After balancing the baseline data of the two groups by PSM (76 cases in each group after matching, total sample 152 cases), the diagnostic value of SII for MACE was analyzed using the ROC curve to determine the optimal threshold value. The independent risk factors for MACE were analyzed using multifactorial Cox regression. Kaplan-Meier curves were employed to compare the MACE-free survival rates of patients with varying SII levels.

resultsPSM effectively balanced the baseline characteristics of the two groups, with absolute values of standardized mean difference for all variables < 0.1. Platelet counts, neutrophil counts, neutrophil-to-lymphocyte ratio, SII, C-reactive protein (CRP), and NT-proBNP levels were significantly higher in the MACE group than in the non-MACE group (P < 0.05). The ROC curve showed that the area under the curve (AUC) of SII after PSM was 0.788 (95% CI 0.714-0.860, P < 0.001), with an optimal threshold of 589.31 (sensitivity 81.58%, specificity 65.79%). Multifactorial Cox analysis showed that SII ≥ 589.31 (HR 1.92, 95% CI 1.18-3.14, P = 0.009), elevated CRP (HR 1.12, 95% CI 1.03-1.23, P = 0.010), and NT-proBNP (HR 1.01, 95% CI 1.01-1.01, P < 0.001) were independent risk factors for MACE. Kaplan-Meier analysis showed that the incidence of MACE was significantly higher in the high SII (≥ 589.31) group than in the low SII group (69.30% vs 23.40%, P < 0.05).

conclusionsElevated SII increases the risk of MACE in patients with CHD with HF and is associated with poor survival.

Indexed as

Coronary DiseaseHeart FailureInflammationAgedBiomarkersC-Reactive ProteinFemaleHumansMaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsPrognosisPropensity ScoreRisk FactorsROC CurveBiomarkersC-Reactive ProteinNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Coronary artery diseaseHeart failureMajor adverse cardiovascular eventsPropensity score matchingSystemic immunoinflammatory index

Identifiers

PMID40830803
PMCPMC12363026

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.