Wang Minghang, Cai Kunkun, Shi Dingli, Tu Xinmin, Zhao Huanhuan, Li Suyun, Li Jiansheng
Department of Respiratory Diseases, the First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450000, Henan, China.
Respiratory Disease Diagnosis and Treatment and New Drug Research and Development Provincial and Ministry Co-built Collaborative Innovation Center, Henan University of Traditional Chinese Medicine, Henan Key Laboratory of Chinese Medicine for Respiratory Diseases, Zhengzhou 450046, Henan, China. Corresponding author: Li Jiansheng, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2021 Jan;33(1):64-68. doi: 10.3760/cma.j.cn121430-20200720-00534.
To establish a risk prediction model for acute exacerbation of chronic obstructive pulmonary disease (AECOPD) using regression analysis and verify the model.
The risk factors and acute exacerbation of 1 326 patients with chronic obstructive pulmonary disease (COPD) who entered the stable phase and followed up for 6 months in the four completed multi-center large-sample randomized controlled trials were retrospectively analyzed. Using the conversion-random number generator, about 80% of the 1 326 cases were randomly selected as the model group (n = 1 074), and about 20% were the verification group (n = 252). The data from the model group were selected, and Logistic regression analysis was used to screen independent risk factors for AECOPD, and an AECOPD risk prediction model was established; the model group and validation group data were substituted into the model, respectively, and the receiver operating characteristic (ROC) curve was drawn to verify the effectiveness of the risk prediction model in predicting AECOPD.
There were no statistically significant differences in general information (gender, smoking status, comorbidities, education level, etc.), body mass index (BMI) classification, lung function [forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), etc.], disease status (the number and duration of acute exacerbation in the past year, duration of disease, etc.), quality of life scale [COPD assessment test (CAT), etc.] and clinical symptoms (cough, chest tightness, etc.) between the model group and the validation group. It showed that the two sets of data had good homogeneity, and the cases in the validation group could be used to verify the effectiveness of the risk prediction model established through the model group data to predict AECOPD. Logistic regression analysis showed that gender [odds ratio (OR) = 1.679, 95% confidence interval (95%CI) was 1.221-2.308, P = 0.001], BMI classification (OR = 0.576, 95%CI was 0.331-1.000, P = 0.050), FEV1 (OR = 0.551, 95%CI was 0.352-0.863, P = 0.009), number of acute exacerbation (OR = 1.344, 95%CI was 1.245-1.451, P = 0.000) and duration of acute exacerbation (OR = 1.018, 95%CI was 1.002-1.034, P = 0.024) were independent risk factors for AECOPD. A risk prediction model for AECOPD was constructed based on the results of regression analysis: probability of acute exacerbation (P) = 1/(1+e), x = -3.274+0.518×gender-0.552×BMI classification+0.296×number of acute exacerbation+0.018×duration of acute exacerbation-0.596×FEV1. The ROC curve analysis verified that the area under ROC curve (AUC) of the model group was 0.740, the AUC of the verification group was 0.688; the maximum Youden index of the model was 0.371, the corresponding best cut-off value of prediction probability was 0.197, the sensitivity was 80.1%, and the specificity was 57.0%.
The AECOPD risk prediction model based on the regression analysis method had a moderate predictive power for the acute exacerbation risk of COPD patients, and could assist clinical diagnosis and treatment decision in a certain degree.
采用回归分析方法建立慢性阻塞性肺疾病急性加重(AECOPD)风险预测模型并进行验证。
回顾性分析在四项完成的多中心大样本随机对照试验中进入稳定期并随访6个月的1326例慢性阻塞性肺疾病(COPD)患者的危险因素及急性加重情况。利用转换随机数生成器,从1326例病例中随机选取约80%作为模型组(n = 1074),约20%作为验证组(n = 252)。选取模型组数据,采用Logistic回归分析筛选AECOPD的独立危险因素,建立AECOPD风险预测模型;将模型组和验证组数据分别代入模型,绘制受试者工作特征(ROC)曲线,验证风险预测模型预测AECOPD的有效性。
模型组与验证组在一般资料(性别、吸烟状况、合并症、教育程度等)、体重指数(BMI)分级、肺功能[第1秒用力呼气容积(FEV1)、用力肺活量(FVC)等]、疾病状态(过去一年急性加重次数及持续时间、病程等)、生活质量量表[慢性阻塞性肺疾病评估测试(CAT)等]及临床症状(咳嗽、胸闷等)方面差异均无统计学意义。表明两组数据具有良好的同质性,验证组病例可用于验证通过模型组数据建立的风险预测模型预测AECOPD的有效性。Logistic回归分析显示,性别[比值比(OR)= 1.679,95%置信区间(95%CI)为1.221 - 2.308,P = 0.001]、BMI分级(OR = 0.576,95%CI为0.331 - 1.000)、FEV1(OR = 0.551,95%CI为0.352 - 0.863,P = 0.009)、急性加重次数(OR = 1.344,95%CI为1.245 - 1.451,P = 0.000)及急性加重持续时间(OR = 1.018,95%CI为1.002 - 1.034,P = 0.024)是AECOPD的独立危险因素。根据回归分析结果构建AECOPD风险预测模型:急性加重概率(P)= 1/(1 + e),x = -3.274 + 0.518×性别 - 0.552×BMI分级 + 0.296×急性加重次数 + 0.018×急性加重持续时间 - 0.596×FEV1。ROC曲线分析验证模型组的ROC曲线下面积(AUC)为0.74,验证组的AUC为0.688;模型的最大约登指数为0.371,对应的最佳预测概率截断值为0.197,灵敏度为80.1%,特异度为57.0%。
基于回归分析方法建立的AECOPD风险预测模型对COPD患者急性加重风险具有中等预测能力,在一定程度上可辅助临床诊断和治疗决策。