Bećirović Amir, Becirovic Emir, Becirovic Minela, Begagic Emir, Abdic Admir, Ljuca Kenana, Buljubasic Lemana, Ljuca Nadina, Kasapovic Tarik, Mujaric Ekrema
Department of Endocrinology, University Clinical Center Tuzla, Tuzla, BIH.
Internal Medicine Clinic, Intensive Care Unit, University Clinical Center Tuzla, Tuzla, BIH.
Cureus. 2025 Jul 31;17(7):e89136. doi: 10.7759/cureus.89136. eCollection 2025 Jul.
Background Non-ST-elevation myocardial infarction (NSTEMI) is frequently associated with systemic inflammation and metabolic dysregulation. Indices derived from routine laboratory tests that reflect systemic inflammatory and lipid-inflammatory status may offer better prognostic insight. This study aimed to evaluate the association between selected indices and short-term major adverse cardiovascular events (MACE) and all-cause mortality in patients with NSTEMI treated with dual antiplatelet therapy (DAPT) and statin. The selected indices reflect key mechanisms involved in NSTEMI pathophysiology, including insulin resistance, atherogenic dyslipidemia, and inflammation. Materials and methods This prospective observational study included 171 patients with NSTEMI admitted to the Intensive Care Unit of the Clinic for Internal Medicine at the University Clinical Centre Tuzla between February 1, 2022, and January 31, 2023. Blood samples were collected upon admission and 24 hours subsequently. The following indices were calculated: triglyceride-glucose index (TyG), triglyceride-to-high-density lipoprotein ratio (TG/HDL), atherogenic index of plasma (AIP), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and pan-immune-inflammation value (PIV). Outcomes were tracked during hospitalization and up to three months post-discharge. MACE was defined as cardiovascular death, reinfarction, stroke, or unplanned revascularization. All patients underwent coronary angiography; revascularization was performed when clinically indicated. Exclusion criteria included active malignancy, infection, or inflammatory disease. Logistic regression was adjusted for age, diabetes, and other clinical variables. Missing data were handled using the pairwise deletion method. Results High levels of TyG at admission were independently associated with MACE (odds ratio (OR) 1.7; 95% confidence interval (CI) 1.0-2.8; p = 0.037). All-cause mortality occurred in 14.6% of patients (n = 25), while MACE occurred in 60 patients. Independent predictors of mortality included elevated TyG at admission (OR 2.2; 95% CI 1.1-4.4; p = 0.034), TG/HDL at 24 hours (OR 1.4; 95% CI 1.1-1.7; p = 0.007), AIP at 24 hours (OR 5.7; 95% CI 1.1-28.9; p = 0.035), and NLR at 24 hours (OR 1.1; 95% CI 1.0-1.2; p = 0.002). PLR and PIV at 24 hours were also significantly associated with mortality. Optimal cut-off values were TyG ≥ 8.9, AIP ≥ 0.35, and NLR ≥ 4.5. NLR had the highest estimated area under the curve (AUC ≈ 0.78). Conclusion In NSTEMI patients treated with DAPT and statin, several inflammatory and lipid-inflammatory indices were independently associated with short-term mortality. Indices measured at 24 hours had a stronger prognostic value than baseline values. Serial monitoring may aid early risk stratification. Outcomes were assessed during hospitalization and via structured follow-up up to three months post-discharge.
非ST段抬高型心肌梗死(NSTEMI)常与全身炎症和代谢失调相关。源自常规实验室检查的反映全身炎症和脂质炎症状态的指标可能提供更好的预后洞察。本研究旨在评估选定指标与接受双联抗血小板治疗(DAPT)和他汀类药物治疗的NSTEMI患者的短期主要不良心血管事件(MACE)及全因死亡率之间的关联。选定指标反映了NSTEMI病理生理学中涉及的关键机制,包括胰岛素抵抗、致动脉粥样硬化性血脂异常和炎症。
这项前瞻性观察性研究纳入了2022年2月1日至2023年1月31日期间入住图兹拉大学临床中心内科重症监护病房的171例NSTEMI患者。入院时及随后24小时采集血样。计算以下指标:甘油三酯-葡萄糖指数(TyG)、甘油三酯与高密度脂蛋白比值(TG/HDL)、血浆致动脉粥样硬化指数(AIP)、中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)以及全免疫炎症值(PIV)。在住院期间及出院后长达三个月跟踪结局。MACE定义为心血管死亡、再梗死、中风或计划外血管重建。所有患者均接受冠状动脉造影;在临床指征明确时进行血管重建。排除标准包括活动性恶性肿瘤、感染或炎症性疾病。逻辑回归针对年龄、糖尿病和其他临床变量进行了调整。使用成对删除法处理缺失数据。
入院时TyG水平高与MACE独立相关(比值比(OR)1.7;95%置信区间(CI)1.0 - 2.8;p = 0.037)。14.6%的患者(n = 25)发生全因死亡,60例患者发生MACE。死亡率的独立预测因素包括入院时TyG升高(OR 2.2;95% CI 1.1 - 4.4;p = 0.034)、24小时时的TG/HDL(OR 1.4;95% CI 1.1 - 1.7;p = 0.007)、24小时时的AIP(OR 5.7;95% CI 1.1 - 28.9;p = 0.035)以及24小时时的NLR(OR 1.1;95% CI 1.0 - 1.2;p = 0.002)。24小时时的PLR和PIV也与死亡率显著相关。最佳截断值为TyG≥8.9、AIP≥0.35和NLR≥4.5。NLR的曲线下面积估计值最高(AUC≈0.78)。
在接受DAPT和他汀类药物治疗的NSTEMI患者中,多个炎症和脂质炎症指标与短期死亡率独立相关。24小时时测量的指标比基线值具有更强的预后价值。连续监测可能有助于早期风险分层。通过结构化随访在住院期间及出院后长达三个月评估结局。