利用机器学习预测心房颤动的多方面风险:来自 GLORIA-AF 研究的启示

Juan Lu, A. Bisson, Mohammed Bennamoun, Yalin Zheng, Frank M. Sanfilippo, Joseph Hung, Tom Briffa, Brendan M. McQuillan, J. Stewart, Gemma Figtree, M. V. Huisman, Girish Dwivedi, G. Y. Lip
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引用次数: 0

摘要

心房颤动(房颤)患者发生缺血性中风和死亡的风险较高。虽然抗凝药物能有效降低这些风险,但会增加出血风险。目前的临床风险评分在预测不良预后方面表现一般,尤其是在预测死亡预后方面。我们旨在测试多标签梯度提升决策树(ML-GBDT)模型在前瞻性全球房颤登记中预测不良后果风险的能力。 我们对 2011 年至 2020 年间 GLORIA-AF 登记的 II/III 期患者进行了研究。结果包括房颤后一年内的全因死亡、缺血性中风和大出血。我们训练了 ML-GBDT 模型,并比较了它与临床评分在预测患者预后方面的区别。共纳入 25656 名患者(平均年龄 70.3 岁(标清 10.3);44.8% 为女性)。房颤后一年内,215 名患者(0.8%)发生缺血性中风,405 名患者(1.6%)发生大出血,897 名患者(3.5%)死亡。在预测死亡(0.785,95% CI:0.757-0.813)、缺血性中风(0.691,0.626-0.与 CHA2DS2-VASc 相比(0.613,p=0.028),大出血(0.698,0.651-0.745)与 HAS-BLED 相比(0.607,p=0.002),净重分类指数有所改善(分别为 10.0%、12.5% 和 23.6%)。 ML-GBDT 模型在预测房颤患者的风险方面优于临床风险评分。这种方法可作为一种单一的多方面综合工具,在管理房颤时优化患者风险评估并减轻不良后果。
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Predicting multifaceted risks using machine learning in Atrial Fibrillation: Insights from GLORIA-AF study
Patients with atrial fibrillation (AF) have a higher risk of ischaemic stroke and death. While anticoagulants are effective at reducing these risks, they increase the risk of bleeding. Current clinical risk scores only perform modestly in predicting adverse outcomes, especially for the outcome of death. We aimed to test the multi-label gradient boosting decision tree (ML-GBDT) model in predicting risks for adverse outcomes in a prospective global AF registry. We studied patients from phase II/III of the GLORIA-AF registry between 2011 and 2020. The outcomes were all-cause death, ischaemic stroke and major bleeding within one year following the AF. We trained the ML-GBDT model and compared its discrimination with the clinical scores in predicting patient outcomes. A total of 25,656 patients were included (mean age 70.3 years (SD 10.3); 44.8% female). Within one-year after AF, ischaemic stroke occurred in 215 (0.8%), major bleeding in 405 (1.6%), and death in 897 (3.5%) patients. Our model achieved an optimized area under the curve (AUC) in predicting death (0.785, 95% CI: 0.757-0.813) compared to Charlson Comorbidity Index (0.747, p=0.007), ischaemic stroke (0.691, 0.626-0.756) comparing to CHA2DS­2-VASc (0.613, p=0.028), and major bleeding (0.698, 0.651-0.745) as opposed to HAS-BLED (0.607, p=0.002), with improvement in net reclassification index (10.0%, 12.5% and 23.6% respectively). The ML-GBDT model outperformed clinical risk scores in predicting the risks in patients with AF. This approach could be used as a single multifaceted holistic tool to optimize patient risk assessment and mitigate adverse outcomes when managing AF.
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