Risk stratification at prediabetes onset and association with diabetes outcomes using EHR data.

Junjie Luo, Di Hu, Rui Han, Diyang Lyu, Ritu Agarwal, Nestoras Mathioudakis, Jehan El-Bayoumi, Gordon Gao, Nawar Shara
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Abstract

Prediabetes can progress to type 2 diabetes (T2D), but individual risk varies widely. Few studies have rigorously characterized subgroups at the point of prediabetes (PD) onset. Using electronic health records (EHRs), we developed a machine learning approach to stratify PD and analyze T2D progression risk. We defined PD onset based on strict HbA1c criteria and excluded patients with missing follow-ups or atypical clinical events, yielding a high-fidelity cohort of 14,436 patients from an initial pool of 74,054 (2017-2023, MedStar Health). An XGBoost model using routine features, including HbA1c, BMI, blood pressure, lipids, ALT, medication history, and lifestyle factors, was trained on 2018-2020 data and tested on 2021-2022 patients, achieving an AUC of 81.6%. Risk scores enabled subtyping into high-, medium-, and low-risk groups with distinct progression trajectories. Stratification patterns remained consistent in future cohorts. This approach supports earlier, personalized intervention and diabetes risk prediction using real-world EHR data.

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使用电子病历数据进行糖尿病前期发病的风险分层及其与糖尿病结局的关联。
前驱糖尿病可发展为2型糖尿病(T2D),但个体风险差异很大。很少有研究严格地描述了糖尿病前期(PD)发病时的亚群。使用电子健康记录(EHRs),我们开发了一种机器学习方法来分层PD并分析T2D进展风险。我们根据严格的HbA1c标准定义了PD发病,并排除了缺少随访或非典型临床事件的患者,从最初的74054例患者中获得了14436例高保真队列(2017-2023年,MedStar Health)。XGBoost模型使用常规特征,包括HbA1c、BMI、血压、血脂、ALT、用药史和生活方式因素,对2018-2020年的数据进行训练,并对2021-2022年的患者进行测试,AUC为81.6%。风险评分使亚型分为具有不同进展轨迹的高、中、低风险组。分层模式在未来的队列中保持一致。这种方法支持使用真实世界的电子病历数据进行早期、个性化干预和糖尿病风险预测。
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