基于机器学习的社区中老年人肌肉疏松症预测:CHARLS 的研究结果。

IF 1.7
Zongjie Wang, Yafei Wu, Junmin Zhu, Ya Fang
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引用次数: 0

摘要

背景:肌肉疏松症是老龄化人群中的一个突出问题,与不良的健康状况有关。本研究旨在探讨问卷调查和生物标志物数据对肌肉疏松症的预测价值,并进一步为社区中老年人开发一款用户友好型计算器:我们利用中国健康与退休纵向研究(CHARLS)的两次波次(2011 年和 2013 年)来预测 "肌肉疏松症",其定义符合 "亚洲肌肉疏松症工作组 2019 年标准"。我们将分析样本限定为 45 岁或以上的成年人(N = 2934)。我们使用了五种机器学习模型来构建 Q 型(仅问卷变量)、Bio 型(仅生物标志物变量)和组合型(问卷加生物标志物变量)模型。采用接收者工作特征曲线下面积(AUROC)进行性能评估。根据 CHARLS 的两个数据集进行了时间外部验证。通过 Shapley 值和系数确定了重要的预测因子:在测试集上,当决策阈值为 0.20 时,其 AUROC 为 0.759(95% CI:0.747-0.771)。模型在外部数据集上也表现良好。我们发现,在基于 Q 的模型和组合模型中,认知功能是最重要的预测因素,而在基于 Bio 的模型中,血尿素氮是最重要的预测因素。其他重要的预测因素包括教育程度、血细胞比容、总胆固醇、饮酒、慢性病数量和日常生活工具活动评分:我们的研究结果为在社区环境中早期筛查和有针对性地预防中老年人肌肉疏松症提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Machine learning-based prediction of sarcopenia in community-dwelling middle-aged and older adults: findings from the CHARLS.

Background: Sarcopenia is a prominent issue among aging populations and associated with poor health outcomes. This study aimed to examine the predictive value of questionnaire and biomarker data for sarcopenia, and to further develop a user-friendly calculator for community-dwelling middle-aged and older adults.

Methods: We used two waves (2011 and 2013) of the China Health and Retirement Longitudinal Study (CHARLS) to predict sarcopenia, defined by the Asian Working Group for Sarcopenia 2019 criteria. We restricted the analytical sample to adults aged 45 or above (N = 2934). Five machine learning models were used to construct Q-based (only questionnaire variables), Bio-based (only biomarker variables), and combined (questionnaire plus biomarker variables) models. Area under the receiver operating characteristic curve (AUROC) was used for performance assessment. Temporal external validation was performed based on two datasets from CHARLS. Important predictors were identified by Shapley values and coefficients.

Results: Extreme gradient boosting (XGBoost), considering both questionnaire and biomarker characteristics, emerged as the optimal model, and its AUROC was 0.759 (95% CI: 0.747-0.771) at a decision threshold of 0.20 on the test set. Models also performed well on the external datasets. We found that cognitive function was the most important predictor in both Q-based and combined models, and blood urea nitrogen was the most important predictor in the Bio-based model. Other key predictors included education, haematocrit, total cholesterol, drinking, number of chronic diseases, and instrumental activities of daily living score.

Conclusions: Our findings offer a potential for early screening and targeted prevention of sarcopenia among middle-aged and older adults in the community setting.

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