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基于空气传播变应原特异性IgE检测结果构建儿童过敏性哮喘诊断预测模型

[Construction of a diagnostic prediction model for childhood allergic asthma based on the detection results of specific IgE for airborne allergens].

作者信息

Yue C Y, Xiang L, Hou X L, Huang H J

机构信息

Department of Allergy,Beijing Children's Hospital,Allergy Disease Professional Committee of the National Center for Monitoring of Infectious and Allergic Diseases in Children,Capital Medical University/National Center for Children's Health/Key Laboratory of Major Diseases in Children,Ministry of Education/National Clinical Research Center for Respiratory Diseases,Beijing 100045,China.

出版信息

Zhonghua Yu Fang Yi Xue Za Zhi. 2025 May 6;59(5):658-666. doi: 10.3760/cma.j.cn112150-20250210-00098.

Abstract

To construct a diagnostic prediction model for childhood asthma and conduct a preliminary evaluation based on the test results of specific IgE (sIgE) for airborne allergens and in combination with clinical data. This study is a case-control study. A total of 4 338 cases that completed the sIgE test for airborne allergens in the Allergy Department of Beijing Children's Hospital Affiliated to Capital Medical University from January to December 2023 were selected as the research subjects. They were divided into the asthma group and the non-asthma group based on the diagnostic information. Age, gender, cough and wheezing symptoms, and the classification results of sIgE concentrations of 15 airborne allergens were collected as the predictor variables of the asthma diagnostic prediction model. Differential analysis and LASSO regression were employed for the screening of predictor variables. The multivariate logistic regression method was applied to construct the nomogram prediction model. The data set was randomly split at a ratio of 7∶3 into a training set (3 036 cases) for constructing the prediction model and a validation set (1 302 cases) for testing the predictive efficacy of the model. The area under the receiver operating characteristic (ROC) curve (AUC), the Hosmer-Lemeshow calibration curve were utilized to assess the discrimination and goodness of fit of the model, and the clinical decision curve (DCA) was adopted to evaluate the clinical application value of the model. Among 4 338 pediatric cases, children aged 0 to <3 years accounted for 10.17% (441 cases), those aged 3 to <6 years accounted for 36.49% (1 583 cases), those aged 6 to <12 years accounted for 46.98% (2 038 cases), and those aged 12 to 18 years accounted for 6.36% (276 cases). Males constituted 65.17% (2 827 cases), and females 34.83% (1 511 cases). The proportion of children without wheezing symptoms was 41.47% (1 799 cases), while those with wheezing symptoms was 58.53% (2 539 cases). The asthma group accounted for 41.77% (1 812 cases), and the non-asthma group for 58.23% (2 526 cases). Statistically significant differences were observed between the asthma group and the non-asthma group in 18 predictive variables including age, gender, wheezing symptoms, d1, d2, e1, e5, g2, g6, m6, t11, t3, t6, w1, w22, w6, wx5, and m3 (<0.05). LASSO regression analysis identified six predictor variables: age (calculated in months), cough and wheezing symptoms, and sIgE of four airborne allergens, namely, Dermatophagoides pteronyssinus (d1), Canis familiaris dander (e5), Aspergillus fumigatus (m3), and Artemisia vulgaris pollen (w6).Multifactorial regression analysis revealed that the contribution degrees of the above-mentioned predictor variables to the asthma diagnosis prediction model were ranked as follows: cough and wheezing symptoms (=24.37, 0.001), m3 (1.34, <0.001), d1 (=1.22, 0.001), e5 (=1.12, 0.028), w6 (=1.11, 0.001), and age (=1.01, 0.001).The AUCs of the nomogram prediction model for the training set and the validation set were 0.853 (95% 0.840-0.866) and 0.838 (95%: 0.817-0.860), respectively. The Hosmer-Lemeshow calibration curve indicated a good fit (=0.215 for the training set; =0.352 for the validation set). The DCA of the validation set demonstrated that when the probability threshold for predicting the occurrence of childhood asthma was 8%-92%, the model had the best applicability. By combining age, cough and wheezing symptoms, and sIgE of the four airborne allergens (d1, e5, m3, and w6) selected from 15 airborne allergens, a childhood asthma diagnosis prediction model with good predictive performance and clinical practicability was constructed. It can serve as a simple and convenient tool for accurately identifying asthma and provides a practical basis for the application of artificial intelligence big data analysis models in the prevention, treatment, and management of childhood asthma.

摘要

构建儿童哮喘诊断预测模型,并根据空气中变应原特异性IgE(sIgE)检测结果并结合临床数据进行初步评估。本研究为病例对照研究。选取2023年1月至12月在首都医科大学附属北京儿童医院过敏科完成空气中变应原sIgE检测的4338例患儿作为研究对象。根据诊断信息将其分为哮喘组和非哮喘组。收集年龄、性别、咳嗽和喘息症状以及15种空气中变应原sIgE浓度的分类结果作为哮喘诊断预测模型的预测变量。采用差异分析和LASSO回归筛选预测变量。应用多因素逻辑回归方法构建列线图预测模型。将数据集按7∶3的比例随机分为用于构建预测模型的训练集(3036例)和用于检验模型预测效能的验证集(1302例)。利用受试者操作特征(ROC)曲线下面积(AUC)、Hosmer-Lemeshow校准曲线评估模型的区分度和拟合优度,并采用临床决策曲线(DCA)评估模型的临床应用价值。在4338例儿科病例中,0至<3岁儿童占10.17%(441例),3至<6岁儿童占36.49%(1583例),6至<12岁儿童占46.98%(2038例),12至18岁儿童占6.36%(276例)。男性占65.17%(2827例),女性占34.83%(1511例)。无喘息症状儿童的比例为41.47%(1799例),有喘息症状儿童的比例为58.53%(2539例)。哮喘组占41.77%(1812例),非哮喘组占58.23%(2526例)。哮喘组与非哮喘组在年龄、性别、喘息症状、d1、d2、e1、e5、g2、g6、m6、t11、t3、t6、w1、w22、w6、wx5和m3这18个预测变量上存在统计学显著差异(<0.05)。LASSO回归分析确定了6个预测变量:年龄(以月计算)、咳嗽和喘息症状以及4种空气中变应原的sIgE,即屋尘螨(d1)、犬皮屑(e5)、烟曲霉(m3)和蒿属花粉(w6)。多因素回归分析显示,上述预测变量对哮喘诊断预测模型的贡献度排序如下:咳嗽和喘息症状(=24.37,0.001)、m3(1.34,<0.001)、d1(=1.22,0.001)、e5(=1.12,0.028)、w6(=1.11,0.001)和年龄(=1.01,0.001)。列线图预测模型在训练集和验证集的AUC分别为0.853(95%:0.840 - 0.866)和0.838(95%:0.817 - 0.860)。Hosmer-Lemeshow校准曲线显示拟合良好(训练集=0.215;验证集=0.352)。验证集的DCA表明,当预测儿童哮喘发生的概率阈值为8% - 92%时,模型具有最佳适用性。通过结合从15种空气中变应原中筛选出的年龄、咳嗽和喘息症状以及4种空气中变应原(d1、e5、m3和w6)的sIgE,构建了具有良好预测性能和临床实用性的儿童哮喘诊断预测模型。它可作为准确识别哮喘的简单便捷工具,并为人工智能大数据分析模型在儿童哮喘预防、治疗和管理中的应用提供实践依据。

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