Department of Clinical Pharmacy, The First Hospital of Hebei Medical University, Shijiazhuang, 050017, People's Republic of China.
The Technology Innovation Center for Artificial Intelligence in Clinical Pharmacy of Hebei Province, The First Hospital of Hebei Medical University, Shijiazhuang, 050017, People's Republic of China.
Int J Clin Pharm. 2024 Aug;46(4):926-936. doi: 10.1007/s11096-024-01729-7. Epub 2024 May 11.
Venlafaxine dose regimens vary considerably between individuals, requiring personalized dosing.
This study aimed to identify dose-related influencing factors of venlafaxine through real-world data analysis and to construct a personalized dose model using advanced artificial intelligence techniques.
We conducted a retrospective study on patients with depression treated with venlafaxine. Significant variables were selected through a univariate analysis. Subsequently, the predictive performance of seven models (XGBoost, LightGBM, CatBoost, GBDT, ANN, TabNet, and DT) was compared. The algorithm that demonstrated optimal performance was chosen to establish the dose prediction model. Model validation used confusion matrices and ROC analysis. Additionally, a dose subgroup analysis was conducted.
A total of 298 patients were included. TabNet was selected to establish the venlafaxine dose prediction model, which exhibited the highest performance with an accuracy of 0.80. The analysis identified seven crucial variables correlated with venlafaxine daily dose, including blood venlafaxine concentration, total protein, lymphocytes, age, globulin, cholinesterase, and blood platelet count. The area under the curve (AUC) for predicting venlafaxine doses of 75 mg, 150 mg, and 225 mg were 0.90, 0.85, and 0.90, respectively.
We successfully developed a TabNet model to predict venlafaxine doses using real-world data. This model demonstrated substantial predictive accuracy, offering a personalized dosing regimen for venlafaxine. These findings provide valuable guidance for the clinical use of the drug.
文拉法辛的剂量方案在个体之间差异很大,需要进行个体化给药。
本研究旨在通过真实世界数据分析确定文拉法辛的剂量相关影响因素,并利用先进的人工智能技术构建个体化剂量模型。
我们对接受文拉法辛治疗的抑郁症患者进行了回顾性研究。通过单因素分析选择有意义的变量。随后,比较了七种模型(XGBoost、LightGBM、CatBoost、GBDT、ANN、TabNet 和 DT)的预测性能。选择表现最佳的算法来建立剂量预测模型。使用混淆矩阵和 ROC 分析进行模型验证。此外,还进行了剂量亚组分析。
共纳入 298 例患者。选择 TabNet 建立文拉法辛剂量预测模型,其性能最佳,准确率为 0.80。分析确定了与文拉法辛日剂量相关的七个关键变量,包括血中文拉法辛浓度、总蛋白、淋巴细胞、年龄、球蛋白、胆碱酯酶和血小板计数。预测 75mg、150mg 和 225mg 文拉法辛剂量的曲线下面积(AUC)分别为 0.90、0.85 和 0.90。
我们成功地使用真实世界数据开发了 TabNet 模型来预测文拉法辛的剂量。该模型表现出较高的预测准确性,为文拉法辛提供了个体化给药方案。这些发现为该药物的临床应用提供了有价值的指导。