武汉大学中南医院呼吸与危重症医学科 湖北 武汉 430071
杨双,女,1993—,医学硕士,主治医师,主要从事肺纤维化相关研究,E‑mail:202324337@163.com
江红霞,女,1992—,医学博士,主要从事肺动脉高压发病机制相关研究,E‑mail:Jianghx@whu.edu.cn
朱明辉,E‑mail:zhuming_1992@126.com
程真顺,E‑mail:Chzs1990@163.com。
收稿:2025-05-16,
纸质出版:2026-10-25
移动端阅览
杨双,江红霞,朱明辉等.特发性肺纤维化生存预后预测模型的建立及验证[J].武汉大学学报(医学版),2026,47(10):1372-1381.
YANG Shuang,JIANG Hongxia,ZHU Minghui,et al.Construction and validation of the prediction model for survival prognosis of idiopathic pulmonary fibrosis[J].Medical Journal of Wuhan University,2026,47(10):1372-1381.
杨双,江红霞,朱明辉等.特发性肺纤维化生存预后预测模型的建立及验证[J].武汉大学学报(医学版),2026,47(10):1372-1381. DOI: 10.14188/j.1671-8852.2026.0806.
YANG Shuang,JIANG Hongxia,ZHU Minghui,et al.Construction and validation of the prediction model for survival prognosis of idiopathic pulmonary fibrosis[J].Medical Journal of Wuhan University,2026,47(10):1372-1381. DOI: 10.14188/j.1671-8852.2026.0806.
目的
2
探讨多种血液学和生化指标对特发性肺纤维化(IPF)总体生存期(OS)的预测价值,构建列线图模型以实现个体化预后分层。
方法
2
回顾性队列研究纳入2014年1月至2024年8月武汉大学中南医院呼吸与危重症医学科收治的确诊IPF患者894例,收集相关指标。最终纳入研究297例,随机分为训练组(208例)及验证组(89例),训练组进行Cox回归结合临床意义及共线性处理构建列线图模型并验证其预测能力。
结果
2
构建IPF患者列线图模型,进行时间依赖性受试者工作特征(ROC)曲线分析,结果显示,在训练组中,1年、3年、5年OS的曲线下面积(
AUC)
为0.824、0.706、0.666;验证组中,由于样本量限制,1年OS的
AUC
无法可靠估算,3年、5年OS的
AUC
为0.652、0.596。提示短期生存预测能力较强。显示列线图C指数均高于性别⁃年龄⁃生理变量(GAP)模型(训练组中,列线图模型及GAP模型的C指数分别为0.653、0.564;在验证组中,列线图模型及GAP模型的C指数分别为0.593、0.563),提示列线图模型预测能力优于GAP模型。
结论
2
构建的列线图模型可实现IPF患者OS的个体化风险评估。该模型与传统GAP评分系统相比更优,有望用于临床风险分层与随访决策,具有一定应用价值。
Objective
2
To explore the predictive value of multiple hematological and biochemical indicators for overall survival in patients with idiopathic pulmonary fibrosis (IPF)
and to establish a nomogram model to achieve individualized prognostic stratification.
Methods
2
This retrospective cohort study enrolled 894 patients diagnosed with IPF admitted to the Department of Respiratory and Critical Care Medicine
Zhongnan Hospital of Wuhan University from January 2014 to August 2024
and collected relevant clinical indicators. A total of 297 patients were finally included in the analysis. The enrolled subjects were randomly divided into a training cohort (208 patients
70%) and a validation cohort (89 patients
30%). Based on the training cohort
Cox regression analysis
combined with clinical significance evaluation and collinearity assessment
was performed to construct a nomogram model
whose predictive performance was subsequently validated.
Results
2
A nomogram model for patients with IPF was constructed
and time⁃dependent receiver operating characteristic (ROC) curve analysis was performed. The results showed that the area under the curve (
AUC
) values for 1⁃
3⁃
and 5⁃year overall survival in the training cohort were 0.824
0.706
and 0.666
respectively. Due to the limited sample size of the validation cohort
the AUC of 1⁃year OS could not be reliably estimated; the AUC values for 3⁃ and 5⁃year OS were 0.652 and 0.596
respectively. The C⁃index of the nomogram was higher than that of the Gender⁃Age⁃Physiology (GAP) model. In the training cohort
the C⁃indexes of the nomogram model and GAP model were 0.653 and 0.564
respectively. In the validation cohort
the C⁃indexes of the nomogram model and GAP model were 0.593 and 0.563
respectively
demonstrating that the nomogram model possessed better predictive ability compared with the GAP model.
Conclusion
2
The established nomogram model enables individualized risk assessment of overall survival in IPF patients. Compared with the traditional GAP scoring system
this model has better predictive performance
which is expected to be applied in clinical risk stratification and follow‑up decision‑making
and has potential clinical value.
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