Beyond Conventional Blood Parameters: Novel Hematologic Indices for Interpretable Artificial Intelligence in Acute Myocardial Infarction

超越传统血液参数:用于急性心肌梗死可解释人工智能的新型血液学指标

阅读:1

Abstract

OBJECTIVE: Acute myocardial infarction (AMI) is a leading cause of morbidity and mortality worldwide, emphasizing the need for timely and accurate diagnosis. This study evaluates the diagnostic potential of newly derived hematological indices-mean platelet volume-to-platelet count ratio (MPR), platelet-to-white blood cell ratio (PWR), red cell distribution width-to-lymphocyte ratio (RLR), red cell distribution width-to-platelet ratio (RPR), Systemic Immune-Inflammation Index (SII), Systemic Inflammation Response Index (SIRI), and derived neutrophil-to-lymphocyte ratio (dNLR)-combined with conventional blood parameters. MATERIALS AND METHODS: An open-access dataset with 981 participants (477 AMI patients and 504 healthy controls) was analyzed. Feature selection was performed using the ReliefF algorithm to identify the most informative features. At the same time, class imbalance was addressed using the Synthetic Minority Oversampling Technique (SMOTE) for multi-class classification (control, ST-elevation myocardial infarction [STEMI], and non-ST-elevation myocardial infarction [NSTEMI]). Random Forest (RF) and Adaptive Boosting (AdaBoost) classifiers were utilized for both binary and multi-class tasks. RESULTS: In binary classification (Control vs. AMI), RF achieved 84.92% accuracy and 91.25% area under the curve (AUC), while balanced multi-class classification reached 80.75% accuracy with RF, demonstrating consistent and robust performance across cross-validation folds. CONCLUSION: The findings highlight the added value of derived indices that reflect systemic inflammation, immune response, and platelet activity in enhancing the diagnosis of AMI. The proposed framework offers a reliable, interpretable, and clinically applicable approach to support early detection.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。