机器学习能否揭示复杂冠状动脉疾病中预测长期死亡率的未知、临床重要因素?呼吁“大数据”。

IF 3.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Kai Ninomiya, Shigetaka Kageyama, Scot Garg, Shinichiro Masuda, Nozomi Kotoku, Pruthvi C Revaiah, Neil O'leary, Yoshinobu Onuma, Patrick W Serruys
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引用次数: 2

摘要

目的:危险分层和个体风险预测在复杂冠状动脉疾病(CAD)患者的治疗决策中发挥关键作用。本研究的目的是评估机器学习(ML)算法是否可以提高鉴别能力,并在复杂CAD患者经皮冠状动脉介入治疗或冠状动脉旁路移植术后预测长期死亡率时识别未预料到但潜在重要的因素。方法和结果:为了预测长期死亡率,将ML算法应用于SYNTAXES数据库,该数据库包含75个手术前变量,包括人口统计学和临床因素、血液采样、影像学和患者报告的结果。在syntax试验的衍生队列中,使用10倍交叉验证方法评估ML模型的判别能力和特征重要性。在交叉验证中,ML模型显示出可接受的区分(曲线下面积= 0.76)。c反应蛋白、患者报告的手术前精神状态、γ -谷氨酰转移酶和HbA1c被确定为预测10年死亡率的重要变量。结论:ML算法揭示了冠心病患者长期死亡率的未预料到但潜在重要的预后因素。基于大量随机或非随机数据的“大型分析”,即所谓的“大数据”,可能有必要证实这些发现。临床试验注册:syntaxsclinicaltrials .gov参考号:NCT03417050, SYNTAX ClinicalTrials.gov参考号:NCT00114972。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Can machine learning unravel unsuspected, clinically important factors predictive of long-term mortality in complex coronary artery disease? A call for 'big data'.

Can machine learning unravel unsuspected, clinically important factors predictive of long-term mortality in complex coronary artery disease? A call for 'big data'.

Can machine learning unravel unsuspected, clinically important factors predictive of long-term mortality in complex coronary artery disease? A call for 'big data'.

Aims: Risk stratification and individual risk prediction play a key role in making treatment decisions in patients with complex coronary artery disease (CAD). The aim of this study was to assess whether machine learning (ML) algorithms can improve discriminative ability and identify unsuspected, but potentially important, factors in the prediction of long-term mortality following percutaneous coronary intervention or coronary artery bypass grafting in patients with complex CAD.

Methods and results: To predict long-term mortality, the ML algorisms were applied to the SYNTAXES database with 75 pre-procedural variables including demographic and clinical factors, blood sampling, imaging, and patient-reported outcomes. The discriminative ability and feature importance of the ML model was assessed in the derivation cohort of the SYNTAXES trial using a 10-fold cross-validation approach. The ML model showed an acceptable discrimination (area under the curve = 0.76) in cross-validation. C-reactive protein, patient-reported pre-procedural mental status, gamma-glutamyl transferase, and HbA1c were identified as important variables predicting 10-year mortality.

Conclusion: The ML algorithms disclosed unsuspected, but potentially important prognostic factors of very long-term mortality among patients with CAD. A 'mega-analysis' based on large randomized or non-randomized data, the so-called 'big data', may be warranted to confirm these findings.

Clinical trial registration: SYNTAXES ClinicalTrials.gov reference: NCT03417050, SYNTAX ClinicalTrials.gov reference: NCT00114972.

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