预测成年糖尿病患者感染COVID-19的风险:一种机器学习方法。

IF 2.6
Dean T Eurich, Darren Lau, Weiting Li, Olivia Weaver, Tanya Joon, Ming Ye, Finlay A McAlister, Padma Kaul, Salim Samanani
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引用次数: 0

摘要

目的:开发一种机器学习模型,准确预测加拿大阿尔伯塔省社区居住的1型和/或2型糖尿病成年人感染COVID-19的风险。方法:这项预测监督机器学习研究纳入了2019年4月1日至2021年3月31日期间居住在加拿大阿尔伯塔省的已有糖尿病的成年人(bb0 =18岁)(n=372,055,不包括因移民而导致的n=2,541;最终样本量=369,514)。感兴趣的结果是2020年3月1日至2021年3月1日期间SARS-CoV-2 PCR检测结果阳性。模型特征提取自2015年3月1日至2020年3月1日定期收集的艾伯塔省行政卫生数据。在67%的数据上训练了15种算法,在其余33%的数据上验证了表现最好的算法(Light Gradient Boost Model, LGBoost)。对模型进行了标定,并采用受试者工作特征曲线下面积(AUROC)、精确召回曲线下面积(AUPRC)和阈值分析对模型性能进行了评估。结果:在369514名糖尿病患者中,有140511人接受了检测,其中13082人的SARS-CoV-2检测呈阳性。LGBoost模型包含367个特征,AUROC和AUPRC分别为0.69和0.08。该模型对常见的风险阈值进行了很好的校准(在所有阈值均为0.98),但是在所有阈值上的敏感性和阳性预测值都很低(结论:LGBoost模型缺乏敏感性,无法在临床上用于预测阿尔伯塔省糖尿病患者的SARS-CoV-2感染。可能需要其他数据源来改进来自社区的未来COVID-19预测模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting the risk of COVID-19 among adult patients with diabetes: A machine learning approach.

Objectives: To develop a machine learning model that accurately predicts the risk of acquiring COVID-19 in community-dwelling adults with type 1 and/or type 2 diabetes in Alberta, Canada.

Methods: This predictive supervised machine learning study included adults (>=18 years old) living in Alberta, Canada between April 1st 2019-March 31st 2021 with pre-existing diabetes (n=372,055, excluding n=2,541 due to migration; final sample size=369,514). The outcome of interest was a positive SARS-CoV-2 PCR test result between March 1st, 2020, and March 1st, 2021. Model features were extracted from routinely collected Alberta administrative health data from March 1st 2015 to March 1st 2020. Fifteen algorithms were trained on 67% of the data and the top performer (Light Gradient Boost Model, LGBoost) was validated on the remaining 33%. The model was calibrated, and model performance assessed using area under the receiver operating characteristic curve (AUROC), area under the precision recall curve (AUPRC) and threshold analyses.

Results: Among 369,514 individuals with diabetes, 140,511 were tested of whom 13,082 had a positive SARS-CoV-2 test. The LGBoost model incorporated 367 features with AUROC and AUPRC of 0.69 and 0.08 respectively. The model was well-calibrated for common risk thresholds (<0.2 probability) with high specificity (>=0.98 at all thresholds), however sensitivity and positive predictive values were low at all thresholds (<=0.08 and <=0.18 respectively).

Conclusions: The LGBoost model lacked the sensitivity to be clinically useful in predicting SARS-CoV-2 infection in Albertans with diabetes. Alternative data sources may be required to improve future COVID-19 prediction models from the community.

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