使用淋巴细胞与单核细胞比率预测心血管疾病和全因死亡率:来自可解释的机器学习模型的见解

IF 1.9 Q3 PERIPHERAL VASCULAR DISEASE
Jichao Wu , Die Huang , Jiefang Li , Jingxing Yi , Yu Lei , Jun Yin
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引用次数: 0

摘要

背景心血管疾病(CVD)是全球死亡的主要原因,其发病率和死亡率持续上升。低密度脂蛋白胆固醇(low-density lipoprotein cholesterol, LDL-C)、高密度脂蛋白胆固醇(高密度脂蛋白胆固醇,HDL-C)、血糖等常用的生物标志物虽然应用广泛,但也存在一定的局限性。本研究研究了与炎症相关的简单免疫生物标志物淋巴细胞与单核细胞比率(LMR),以评估其是否可以作为预测心血管疾病慢性炎症的新标志物,并将其与传统生物标志物进行比较。方法:我们对2007年至2018年国家健康与营养检查调查(NHANES)的数据进行了横断面分析,纳入了1518名参与者,中位随访期为150个月。在此期间,522名参与者死亡,其中166人死于心血管疾病。我们采用各种统计方法,包括加权Cox比例风险模型、受限三次样条模型和时变受试者工作特征曲线,来检验LMR与死亡风险之间的关系。结果LMR与心血管疾病发病率呈l型关系。低LMR水平与全因死亡率和心血管死亡率呈负相关。XGBoost模型产生了最佳的性能指标(AUC和F1分数),SHAP值分析表明LMR对心血管疾病的预后有显著影响。非线性分析证实LMR与全因死亡率之间存在稳定的负相关。结论LMR是一种简便实用的预测心血管疾病及其死亡率的指标。低水平的LMR显著增加患者心血管疾病和全因死亡率的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting cardiovascular disease and all-cause mortality using the lymphocyte-to-monocyte ratio: Insights from explainable machine learning models

Background

Cardiovascular disease (CVD) is a leading cause of death globally, with its incidence and mortality rates continuing to rise. While commonly used biomarkers such as low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and blood glucose are widely applied, they have certain limitations. This study investigates the lymphocyte-to-monocyte ratio (LMR), a simple immune biomarker associated with inflammation, to assess whether it can serve as a new marker for predicting chronic inflammation in cardiovascular disease, and compares it to traditional biomarkers.

Methods

We conducted a cross-sectional analysis of data from the National Health and Nutrition Examination Survey (NHANES) from 2007 to 2018, utilizing a cohort of 1518 participants with a median follow-up period of 150 months. During this time, 522 participants died, including 166 from cardiovascular disease. We employed various statistical methods, including weighted Cox proportional hazards models, restricted cubic spline models, and time-varying receiver operating characteristic curves, to examine the association between LMR and mortality risk.

Results

The analysis revealed an L-shaped relationship between LMR and the incidence of cardiovascular disease. Lower LMR levels were negatively correlated with all-cause and cardiovascular mortality. The XGBoost model yielded the best performance metrics (AUC and F1 scores), and SHAP value analysis indicated that LMR significantly contributes to CVD outcomes. Non-linear analyses confirmed a stable negative correlation between LMR and all-cause mortality.

Conclusion

The study concludes that LMR is a simple and practical indicator for predicting cardiovascular disease and its mortality. Low levels of LMR significantly increase the risk of both cardiovascular disease and all-cause mortality in patients.
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