Chen Jun-Wei, Lu Chi-Jie, Yu Chieh-Han, Liu Tzu-Chi, Wu Tzu-En
Department of Medical Education, Linkou Chang Gung Memorial Hospital, Guishan Dist., Taoyuan City 333, Taiwan.
Graduate Institute of Business Administration, Fu Jen Catholic University, New Taipei City 242, Taiwan.
Diagnostics (Basel). 2025 Aug 20;15(16):2096. doi: 10.3390/diagnostics15162096.
: Myopia is a growing global health concern, especially among school-aged children in East Asia. Topical atropine is a key treatment for pediatric myopia control, but individual responses vary, with some children showing rapid progression despite higher doses. This retrospective observational study aims to develop an interpretable machine learning model to predict individualized treatment responses and support personalized clinical decisions, based on data collected over a 3-year period without a control group. : A total of 1545 pediatric eyes treated with topical atropine for myopia control at a single tertiary medical center are analyzed. Classification and regression tree (CART) is constructed to predict changes in spherical equivalent (SE) and identify influencing risk factors. These factors are mainly received treatments for myopia including atropine dosage records, treatment duration, and ophthalmic examinations. Furthermore, decision rules that closely resemble the clinical diagnosis process are provided to assist clinicians with more interpretable insights into personalized treatment decisions. The performance of CART is evaluated by comparing with the benchmark model of least absolute shrinkage and selection operator regression (Lasso) to confirm the practicality of CART usage. : Both the CART and Lasso models demonstrated comparable predictive performance. The CART model identified baseline SE as the primary determinant of myopia progression. Children with a baseline SE more negative than -3.125 D exhibited greater myopic progression, particularly those with prolonged treatment duration and higher cumulative atropine dosage. : Baseline SE has been identified as the key factor affecting SE difference. The generated decision rules from CART demonstrate the use of explainable machine learning in precision myopia management.
近视是一个日益受到全球关注的健康问题,在东亚学龄儿童中尤为突出。局部用阿托品是控制儿童近视的关键治疗方法,但个体反应存在差异,一些儿童即使使用高剂量药物仍出现快速进展。这项回顾性观察研究旨在基于3年期间收集的数据(无对照组),开发一种可解释的机器学习模型,以预测个体化治疗反应并支持个性化临床决策。
对一家三级医疗中心的1545只接受局部用阿托品控制近视的儿童眼睛进行了分析。构建分类与回归树(CART)来预测等效球镜度(SE)的变化并识别影响风险因素。这些因素主要包括近视治疗记录,如阿托品剂量记录、治疗持续时间和眼科检查。此外,还提供了与临床诊断过程非常相似的决策规则,以帮助临床医生对个性化治疗决策有更具可解释性的见解。通过与最小绝对收缩和选择算子回归(Lasso)的基准模型进行比较,评估CART的性能,以确认CART使用的实用性。
CART和Lasso模型均表现出相当的预测性能。CART模型确定基线SE是近视进展的主要决定因素。基线SE比-3.125 D更负的儿童表现出更大的近视进展,特别是那些治疗持续时间长和累积阿托品剂量高的儿童。
基线SE已被确定为影响SE差异的关键因素。从CART生成的决策规则证明了可解释机器学习在精准近视管理中的应用。