布里氏评分
逻辑回归
医学
队列
接收机工作特性
回顾性队列研究
判别式
校准
内科学
预测值
曲线下面积
试验预测值
推导
临床试验
队列研究
回归分析
回归
正谓词值
多元微积分
统计
前瞻性队列研究
医学诊断
肿瘤科
诊断准确性
疾病
作者
Wilfredo Antonio Rivera Martínez,Carlos Esteban Builes-Montaño,Natalia Aristizábal Henao,Stefania Cruz Calderón,Néstor Andrés Díaz Posada,María Johana Ramírez Castaño,Carlos Alfonso Builes Barrera,Claudia Marcela Gómez Serna,Alejandro Román González,Alin Abreu Lomba,Andrés Felipe García Ramos,David Vernaza,Alfonso Soto Moreno,Ana Irigaray Echarri,María Dolores Ollero García-Agulló,María Dolores Moure Rodríguez,Alejandro Pinzón Tovar,Rogelio García-Centeno,L Beltrán Fernández,Andrés Cardona
摘要
The purpose of our study was to develop and externally validate a multivariable diagnostic model to distinguish ectopic ACTH secretion (EAS) from Cushing's disease (CD) using routine clinical parameters. The model was derived from a Spanish multicenter retrospective cohort and externally validated in a Colombian cohort. Predictors were selected through a multivariable logistic regression model with penalized logistic regression (LASSO) using the Spanish cohort. Discriminative performance was assessed using the area under the ROC curve (AUC) and calibration using the slope, the origin, and the Brier score. The derivation cohort included 253 patients from Spain (199 with CD and 54 with EAS). The external validation cohort comprised 72 Colombian patients (53 with CD and 19 with EAS). In the derivation cohort, multivariable modeling identified four independent predictors: ACTH concentration, 24-h urinary free cortisol (UFC), serum potassium, and maximum pituitary tumor diameter. The final model demonstrated good discrimination in the derivation cohort (mean AUC of 0.987), with excellent calibration (calibration slope ranged from 0.998 to 5.22, intercept -0.2 to 0.99, Brier score 0.035). In external validation, model performance remained robust (AUC ranging from 0.9885 to 0.9890; Brier score 0.0381). The model achieved a sensitivity of 95.3%, specificity of 93.6%, positive predictive value of 82.3%, and negative predictive value of 98.7% for detecting EAS. Thus, the diagnostic model developed, based on routinely available clinical variables, shows high accuracy and calibration in differentiating between EAS and CD, supporting its potential use in diverse clinical settings and integration into diagnostic workflows.
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