Predicting the exposure of mycophenolic acid in children with autoimmune diseases using a limited sampling strategy: A retrospective study

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Cts-Clinical and Translational Science Pub Date : 2024-12-27 DOI:10.1111/cts.70092
Ping Zheng, Ting Pan, Ya Gao, Juan Chen, Liren Li, Yan Chen, Dandan Fang, Xuechun Li, Fei Gao, Yilei Li
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Abstract

Mycophenolic acid (MPA) is commonly used to treat autoimmune diseases in children, and therapeutic drug monitoring is recommended to ensure adequate drug exposure. However, multiple blood sampling is required to calculate the area under the plasma concentration-time curve (AUC), causing patient discomfort and waste of human and financial resources. This study aims to use machine learning and deep learning algorithms to develop a prediction model of MPA exposure for pediatric autoimmune diseases with optimizing sampling frequency. Pediatric autoimmune patients' data were collected at Nanfang Hospital between June 2018 and June 2023. Univariate analysis was applied for feature selection. Ten algorithms, including Random Forest, XGBoost, LightGBM, Gradient Boosting Decision Tree, CatBoost, Artificial Neural Network, Grandient Boosting Machine, Transformer, Wide&Deep, and TabNet, were employed for modeling based on two, three, or four concentrations of MPA. A total of 614 MPA AUC0-12h samples from 209 patients were enrolled. Among the 10 models evaluated, the Wide&Deep model exhibited the best predictive performance. The predictive performance of the Wide&Deep model using four and three blood concentration points was similar (R 2 ≈ 1 for four points; R 2 = 0.95 for three points). No significant difference in accuracy within ±30% was observed between models utilizing three and four blood concentration points (p = 0.06). This study demonstrates that in the Wide&Deep model, MPA exposure can be accurately estimated with three sampling points in children with autoimmune diseases. This model could help reduce discomfort in pediatric patients without reducing the accuracy of MPA exposure estimates in clinical practice.

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使用有限抽样策略预测自身免疫性疾病儿童霉酚酸暴露:一项回顾性研究
霉酚酸(MPA)通常用于治疗儿童自身免疫性疾病,建议进行治疗性药物监测以确保足够的药物暴露。但需要多次采血计算血浆浓度-时间曲线下面积(AUC),造成患者不适,浪费人力和财力。本研究旨在利用机器学习和深度学习算法,建立优化采样频率的小儿自身免疫性疾病MPA暴露预测模型。2018年6月至2023年6月在南方医院收集儿童自身免疫性患者的数据。采用单变量分析进行特征选择。采用随机森林(Random Forest)、XGBoost、LightGBM、梯度增强决策树(Gradient Boosting Decision Tree)、CatBoost、人工神经网络(Artificial Neural Network)、granent Boosting Machine、Transformer、Wide&Deep和TabNet等10种算法对2、3、4种浓度的MPA进行建模。共纳入209例患者的614 MPA AUC0-12h样本。在评估的10个模型中,Wide&Deep模型的预测效果最好。采用4个血浓度点和3个血浓度点的Wide&Deep模型的预测性能相似(4个血浓度点的r2≈1;r2 = 0.95(3分)。使用3个血浓度点和4个血浓度点的模型在±30%以内准确率无显著差异(p = 0.06)。本研究表明,在Wide&Deep模型中,自身免疫性疾病儿童的MPA暴露可以通过三个采样点进行准确估计。该模型可以帮助减少儿科患者的不适,而不会降低临床实践中MPA暴露估计的准确性。
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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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