Deng Linfan, Zhao Jian, Wang Ting, Liu Bin, Jiang Jun, Jia Peng, Liu Dong, Li Gang
Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Sichuan Clinical Research Center for Birth Defects, Luzhou, China.
Clin Exp Pediatr. 2024 Aug;67(8):405-414. doi: 10.3345/cep.2024.00549. Epub 2024 Jul 23.
Intravenous immunoglobulin (IVIG)-resistant Kawasaki disease is associated with coronary artery lesion development.
This study aimed to explore the factors associated with IVIG-resistance and construct and validate an interpretable machine learning (ML) prediction model in clinical practice.
Between December 2014 and November 2022, 602 patients were screened and risk factors for IVIG-resistance investigated. Five ML models are used to establish an optimal prediction model. The SHapley Additive exPlanations (SHAP) method was used to interpret the ML model.
Na+, hemoglobin (Hb), C-reactive protein (CRP), and globulin were independent risk factors for IVIG-resistance. A nonlinear relationship was identified between globulin level and IVIG-resistance. The XGBoost model exhibited excellent performance, with an area under the receiver operating characteristic curve of 0.821, accuracy of 0.748, sensitivity of 0.889, and specificity of 0.683 in the testing set. The XGBoost model was interpreted globally and locally using the SHAP method.
Na+, Hb, CRP, and globulin levels were independently associated with IVIG-resistance. Our findings demonstrate that ML models can reliably predict IVIG-resistance. Moreover, use of the SHAP method to interpret the established XGBoost model's findings would provide evidence of IVIG-resistance and guide the individualized treatment of Kawasaki disease.
静脉注射免疫球蛋白(IVIG)抵抗性川崎病与冠状动脉病变发展相关。
本研究旨在探索与IVIG抵抗相关的因素,并构建和验证一个在临床实践中可解释的机器学习(ML)预测模型。
在2014年12月至2022年11月期间,筛选了602例患者并调查了IVIG抵抗的危险因素。使用五个ML模型建立一个最佳预测模型。采用SHapley加法解释(SHAP)方法来解释ML模型。
钠离子(Na+)、血红蛋白(Hb)、C反应蛋白(CRP)和球蛋白是IVIG抵抗的独立危险因素。球蛋白水平与IVIG抵抗之间存在非线性关系。在测试集中,XGBoost模型表现出色,受试者工作特征曲线下面积为0.821,准确率为0.748,灵敏度为0.889,特异性为0.683。使用SHAP方法对XGBoost模型进行了全局和局部解释。
Na+、Hb、CRP和球蛋白水平与IVIG抵抗独立相关。我们的研究结果表明,ML模型可以可靠地预测IVIG抵抗。此外,使用SHAP方法解释所建立的XGBoost模型的结果将为IVIG抵抗提供证据,并指导川崎病的个体化治疗。