临床荟萃 ›› 2026, Vol. 41 ›› Issue (2): 122-127.doi: 10.3969/j.issn.1004-583X.2026.02.004

• 论著 • 上一篇    下一篇

系统免疫炎症指数对射血分数降低型心衰患者发生主要不良心血管事件的预测价值

曹乐1, 赵宇鹏1, 薛凌2()   

  1. 1.锦州医科大学 研究生院,辽宁 锦州 121001
    2.锦州医科大学附属第三医院 全科医学科,辽宁 锦州 121002
  • 收稿日期:2025-12-16 出版日期:2026-02-20 发布日期:2026-03-05
  • 通讯作者: 薛凌,Email:Lysyxueling@163.com

Predictive value of the systemic immune inflammation index for major adverse cardiovascular events in patients with heart failure with reduced ejection fraction

Cao Le1, Zhao Yupeng1, Xue Ling2()   

  1. 1. Graduate School, Jinzhou Medical University, Jinzhou 121001, China
    2. Department of General Practice, the Third Affiliated Hospital of Jinzhou Medical University, Jinzhou 121002, China
  • Received:2025-12-16 Online:2026-02-20 Published:2026-03-05
  • Contact: Xue Ling, Email: Lysyxueling@163.com

摘要:

目的 探讨射血分数降低型心力衰竭(heart failure with reduced ejection fraction, HFrEF)患者主要不良心血管事件(major adverse cardiovascular events, MACE)发生风险的新指标:系统免疫炎症指数(systemic immune inflammation index, SII)。方法 本研究为回顾性分析,连续纳入2022年6月-2024年6月于辽宁省鞍山市中心医院心内科住院的HFrEF患者304例,随访至2025年6月,根据随访期间MACE的发生与否,将患者分为MACE组(n=94)和非MACE组(n=210)。检测并计算两组的实验室指标及相关参数;分析HFrEF患者发生MACE的影响因素;通过单因素和多因素二元logistic回归分析进行数据分析,同时通过ROC曲线下面积(AUC)量化SII对MACE的判别能力。结果 非MACE组和MACE组的基线特征[患者的性别、年龄、体质量指数(BMI)、高血压、糖尿病、经皮冠状动脉介入治疗(PCI)、白细胞计数、肝功能及肾功能指标]差异均无统计学意义(P>0.05)。MACE组吸烟率、中性粒细胞、血小板计数、中性粒细胞与淋巴细胞比值(NLR)、N末端b型钠尿肽前体(NT-proBNP)和SII均高于非MACE组(P<0.05);MACE组淋巴细胞计数及白蛋白水平较非MACE组显著降低,差异有统计学意义(P<0.05);经多因素logistic回归分析,吸烟史和SII与HFrEF患者的MACE风险独立相关(P<0.05)。结论 SII是HFrEF患者发生MACE的独立影响因素,可早期筛查不良预后的高危人群并为其制定相应的预防措施提供参依据。

关键词: 射血分数降低型心力衰竭, 主要不良心血管事件, 系统免疫炎症指数

Abstract:

Objective To evaluate the systemic immune inflammation index (SII) as a novel predictor of major adverse cardiovascular events (MACE) in patients with heart failure with reduced ejection fraction (HFrEF). Methods This retrospective cohort study enrolled 304 consecutive HFrEF patients admitted to the Department of Cardiology, Anshan Central Hospital between June 2022 and June 2024. Patients were followed until June 2025 and categorized according to MACE occurrence during followup into a MACE group (n=94) and a non-MACE group (n=210). Laboratory parameters and related indices were recorded. Univariate and multivariate binary logistic regression analyses were used to identify factors associated with MACE. The discriminative performance of SII for MACE was assessed by receiver operating characteristic (ROC) curve analysis and quantified by the area under the curve (AUC). Results Baseline characteristics, including sex, age, body mass index (BMI), hypertension, diabetes, prior percutaneous coronary intervention (PCI), white blood cell count, and liver and renal function tests, did not differ significantly between groups (P>0.05). Compared with the non-MACE group, the MACE group had higher smoking prevalence, higher neutrophil counts, platelet count, higher neutrophiltolymphocyte ratio (NLR), elevated N-terminal pro-B-type natriuretic peptide (NT-proBNP), and higher SII (all P<0.05), while lymphocyte counts and serum albumin were significantly lower (P<0.05). In multivariate logistic regression, smoking history and SII remained independently associated with MACE risk in HFrEF patients (P<0.05). Conclusion SII is an independent predictor of MACE in patients with HFrEF. Measurement of SII may facilitate early identification of patients at high risk of adverse cardiovascular outcomes and inform targeted preventive strategies.

Key words: heart failure with reduced ejection fraction, major adverse cardiovascular events, systemic immune-inflammation index

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