利用电子健康记录预测阿尔茨海默氏症和相关痴呆症的发病:缓存县老龄记忆研究(1995-2008 年)的发现。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-28 DOI:10.1186/s12911-024-02728-4
Karen C Schliep, Jeffrey Thornhill, JoAnn T Tschanz, Julio C Facelli, Truls Østbye, Michelle K Sorweid, Ken R Smith, Michael Varner, Richard D Boyce, Christine J Cliatt Brown, Huong Meeks, Samir Abdelrahman
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引用次数: 0

摘要

导言:临床笔记、生物标志物和神经影像学已被证明在痴呆症预测模型中很有价值。常见的结构化临床数据能否预测痴呆症是一个新兴的研究领域。我们的目标是利用机器学习方法,在一个表型清晰的人群队列中预测基于研究的金标准痴呆诊断,包括阿尔茨海默病(AD)和/或阿尔茨海默病相关痴呆(ADRD),以及基于 ICD 的 AD 和/或 ADRD 诊断:除了人口普查/病历社会人口学数据(k = 6个特征)外,还将行政医疗保健数据(k = 163个诊断特征)与卡奇县研究(CCS,1995-2008年)进行了链接:在成功连接的UPDB-CCS参与者(n = 4206)中,有522人(12.4%)根据CCS "黄金标准 "评估结果患有痴呆症(单纯AD、AD合并ADRD或单纯ADRD)。随机森林模型的预测窗口期为 1 年,性能最佳,曲线下面积 (AUC) 为 0.67。痴呆症亚型的准确性有所下降:AD/ADDR(AUC = 0.65);ADDR(AUC = 0.49)。当使用基于 ICD 的痴呆诊断时,准确性有所提高(AUC = 0.77):讨论:常见的结构化临床数据(不含实验室、笔记或处方信息)在预测基于研究的 "黄金标准 "AD/ADRD 诊断方面表现出一定的能力,这一点已得到先前研究的证实。与 "黄金标准 "痴呆症诊断相比,大多数机器学习痴呆症预测模型都使用 ICD 诊断代码来识别痴呆症,这可以提高准确率,但这些模型是否能预测真正的痴呆症还需要进一步研究。
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Predicting the onset of Alzheimer's disease and related dementia using electronic health records: findings from the cache county study on memory in aging (1995-2008).

Introduction: Clinical notes, biomarkers, and neuroimaging have proven valuable in dementia prediction models. Whether commonly available structured clinical data can predict dementia is an emerging area of research. We aimed to predict gold-standard, research-based diagnoses of dementia including Alzheimer's disease (AD) and/or Alzheimer's disease related dementias (ADRD), in addition to ICD-based AD and/or ADRD diagnoses, in a well-phenotyped, population-based cohort using a machine learning approach.

Methods: Administrative healthcare data (k = 163 diagnostic features), in addition to census/vital record sociodemographic data (k = 6 features), were linked to the Cache County Study (CCS, 1995-2008).

Results: Among successfully linked UPDB-CCS participants (n = 4206), 522 (12.4%) had incident dementia (AD alone, AD comorbid with ADRD, or ADRD alone) as per the CCS "gold standard" assessments. Random Forest models, with a 1-year prediction window, achieved the best performance with an Area Under the Curve (AUC) of 0.67. Accuracy declined for dementia subtypes: AD/ADRD (AUC = 0.65); ADRD (AUC = 0.49). Accuracy improved when using ICD-based dementia diagnoses (AUC = 0.77).

Discussion: Commonly available structured clinical data (without labs, notes, or prescription information) demonstrate modest ability to predict "gold-standard" research-based AD/ADRD diagnoses, corroborated by prior research. Using ICD diagnostic codes to identify dementia as done in the majority of machine learning dementia prediction models, as compared to "gold-standard" dementia diagnoses, can result in higher accuracy, but whether these models are predicting true dementia warrants further research.

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