The Relationship Between C-Reactive Protein–Triacylglycerol–Glucose Index and All-Cause Mortality in Patients With Cardiovascular Disease: A Retrospective Cohort Study and Development of a Machine Learning Prediction Model

IF 3.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Wenlong Ding, Fachao Shi, Zheng Wang, Long Wang, Caoyang Fang
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引用次数: 0

Abstract

Objective: The CTI is increasingly recognized as a new marker for assessing inflammation and insulin resistance. However, the relationship between CTI and all-cause mortality risk in patients with CVD remains unclear.

Methods: We analyzed data from the NHANES from 1999 to 2010. The correlation between CTI and all-cause mortality risk in CVD patients was examined using Cox regression analysis. Nonlinear relationships between CTI and all-cause mortality risk were explored through restricted cubic splines and Cox proportional hazards regression. We employed six ML models, including RF, LightGBM, DT, XGBoost, LR, and KNN, to predict all-cause mortality risk in CVD patients based on CTI and SHAP for interpretability.

Results: A total of 1429 CVD patients were included, with 849 all-cause deaths recorded during the follow-up period. After adjusting for potential confounding factors, the highest quartile of CTI (Q4) significantly increased the risk of all-cause mortality compared to the lowest quartile (Q1) (HR = 1.38, 95% CI: 1.04–1.84, p = 0.03). Restricted cubic splines demonstrated a nonlinear relationship between CTI and all-cause mortality risk in CVD patients. Among the machine learning models, the LightGBM model exhibited the best predictive performance, with an ROC of 0.967, accuracy of 0.909, sensitivity of 0.906, specificity of 0.914, F1 score of 0.922, recall of 0.906, and PR of 0.979. SHAP analysis identified age, BU, and CTI as the primary predictive factors, with CTI positively correlated with all-cause mortality risk in CVD patients.

Conclusion: There is a nonlinear relationship between CTI and all-cause mortality risk in CVD patients, with elevated CTI levels significantly associated with increased mortality risk. Additionally, for the first time, this study constructed a machine learning model to predict all-cause mortality risk in cardiovascular disease using CTI, with LightGBM demonstrating the best predictive performance. SHAP analysis identified age, BUN, and CTI as critical factors in the prediction, providing valuable references for future related research.

Abstract Image

c -反应蛋白-三酰甘油-葡萄糖指数与心血管疾病患者全因死亡率的关系:回顾性队列研究和机器学习预测模型的开发
目的:CTI越来越被认为是评估炎症和胰岛素抵抗的新标志物。然而,CTI与CVD患者全因死亡风险之间的关系尚不清楚。方法:对1999 - 2010年NHANES数据进行分析。采用Cox回归分析检验CTI与CVD患者全因死亡风险的相关性。通过限制三次样条和Cox比例风险回归探讨CTI与全因死亡风险之间的非线性关系。我们采用六个ML模型,包括RF、LightGBM、DT、XGBoost、LR和KNN,以CTI和SHAP为基础预测CVD患者的全因死亡风险,以提高其可解释性。结果:共纳入1429例CVD患者,随访期间全因死亡849例。在调整了潜在的混杂因素后,与最低四分位数(Q1)相比,CTI最高四分位数(Q4)显著增加了全因死亡的风险(HR = 1.38, 95% CI: 1.04-1.84, p = 0.03)。限制三次样条显示CTI与CVD患者全因死亡风险之间的非线性关系。在机器学习模型中,LightGBM模型的预测性能最好,ROC为0.967,准确率为0.909,灵敏度为0.906,特异性为0.914,F1评分为0.922,召回率为0.906,PR为0.979。SHAP分析发现年龄、BU和CTI为主要预测因素,CTI与CVD患者全因死亡风险呈正相关。结论:CVD患者CTI与全因死亡风险之间存在非线性关系,CTI水平升高与死亡风险增加显著相关。此外,本研究首次构建了一个使用CTI预测心血管疾病全因死亡风险的机器学习模型,其中LightGBM显示出最佳的预测性能。SHAP分析发现年龄、BUN和CTI是预测的关键因素,为今后的相关研究提供了有价值的参考。
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来源期刊
Cardiovascular Therapeutics
Cardiovascular Therapeutics 医学-心血管系统
CiteScore
5.60
自引率
0.00%
发文量
55
审稿时长
6 months
期刊介绍: Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged. Subject areas include (but are by no means limited to): Acute coronary syndrome Arrhythmias Atherosclerosis Basic cardiac electrophysiology Cardiac catheterization Cardiac remodeling Coagulation and thrombosis Diabetic cardiovascular disease Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF) Hyperlipidemia Hypertension Ischemic heart disease Vascular biology Ventricular assist devices Molecular cardio-biology Myocardial regeneration Lipoprotein metabolism Radial artery access Percutaneous coronary intervention Transcatheter aortic and mitral valve replacement.
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