上海市40岁及以上社区人群慢性阻塞性肺疾病发病列线图风险预测模型构建

Development of a nomogram-based risk prediction model for chronic obstructive pulmonary disease incidence in community-dwelling population aged 40 years and above in Shanghai

  • 摘要:
    目的 建立40岁及以上社区人群慢性阻塞性肺疾病(COPD)发病风险预测模型及其列线图,旨在为COPD的筛查和预防提供针对性参考。
    方法 基于上海郊区自然人群队列,随机抽取3 381名40岁及以上队列成员,在2021年7—10月进行肺功能检查,采用Cox逐步回归分析建立总体和分性别风险预测模型,并分别构建风险列线图。使用C指数、曲线下面积(AUC)值和Brier评分评估模型的预测性能,通过10倍交叉验证和敏感性分析评估模型的稳定性。
    结果 最终纳入3 019名研究对象,随访中位时长为4.6年,COPD发病密度为17.22/千人年,男性(32.04/千人年)高于女性(7.38/千人年)(P<0.001)。COPD的总体发病风险预测模型纳入变量为性别、年龄、文化程度、BMI、吸烟和被动吸烟、呼吸共患病。男性预测模型纳入变量为年龄、体重指数(BMI)、呼吸共患病和吸烟。而女性预测模型中纳入变量为年龄、婚姻情况、呼吸共患病和肺结核病史。总体及男女性风险预测模型的C指数分别为0.829、0.749和0.807,预测5年发病风险AUC值分别为0.785、0.658和0.811,Brier评分分别为0.103、0.176和0.059,10倍交叉验证后的C指数及去除随访时间少于6个月研究对象后模型C指数均高于0.740。
    结论 本研究构建了总体和分性别的简洁实用的COPD发病风险预测模型及其列线图,所建立的模型在预测COPD发病风险方面有良好的性能,为识别COPD高危人群、制定筛查和个性化管理方案提供参考。

     

    Abstract:
    Objective To develop a nomogram-based risk prediction model for chronic obstructive pulmonary disease (COPD) incidence among the community-dwelling population aged 40 years old and above, so as to provide targeted references for the screening and prevention of COPD.
    Methods Based on a natural population cohort in suburban Shanghai, a total of 3 381 randomly selected participants aged ≥40 years underwent pulmonary function tests between July and October 2021. Cox stepwise regression analysis was used to develop overall and gender-specific risk prediction models, along with the construction of corresponding risk nomograms. Model predictive performance was evaluated using the C-indice, area under the curve (AUC) values, and Brier score. Stability was assessed through 10-fold cross-validation and sensitivity analysis.
    Results A total of 3 019 participants were included, with a median follow-up duration of 4.6 years. The COPD incidence density was 17.22 per 1 000 person-years, significantly higher in males (32.04/1 000 person-years) than that in females (7.38/1 000 person-years) (P<0.001). The overall risk prediction model included the variables such as gender, age, education level, BMI, smoking, passive smoking, and respiratory comorbidities. The male-specific model incorporated the variables such as age, BMI, respiratory comorbidities, and smoking, while the female-specific model included age, marital status, respiratory comorbidities, and pulmonary tuberculosis history. The C-indices for the overall, male-specific, and female-specific models were 0.829, 0.749, and 0.807, respectively. The 5-year AUC values were 0.785, 0.658, and 0.811, with Brier scores of 0.103, 0.176, and 0.059, respectively. Both 10-fold cross-validated C-indices and sensitivity analysis (excluding participants with a follow-up duration of <6 months) yielded C-indices were above 0.740.
    Conclusion This study developed concise and practical overall and gender-specific COPD risk prediction models and corresponding nomograms. The models demonstrated robust performance in predicting COPD incidence, providing a valuable reference for identifying high-risk populations and formulating targeted screening and personalized management strategies.

     

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