Katsuhiro Iba1,2, Tomohiro Shinozaki3, Kazushi Maruo4, Hisashi Noma5. 1. Department of Statistical Science, School of Multidisciplinary Sciences, The Graduate University for Advanced Studies, Tokyo, Japan. 2. Office of Biostatistics, Department of Biometrics, Headquarters of Clinical Development, Otsuka Pharmaceutical Co., Ltd., Tokyo, Japan. 3. Department of Information and Computer Technology, Faculty of Engineering, Tokyo University of Science, Tokyo, Japan. 4. Department of Biostatistics, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan. 5. Department of Data Science, The Institute of Statistical Mathematics, 10-3 Midori-cho, Tachikawa, Tokyo, 190-8562, Japan. noma@ism.ac.jp.
Abstract
BACKGROUND: Multivariable prediction models are important statistical tools for providing synthetic diagnosis and prognostic algorithms based on patients' multiple characteristics. Their apparent measures for predictive accuracy usually have overestimation biases (known as 'optimism') relative to the actual performances for external populations. Existing statistical evidence and guidelines suggest that three bootstrap-based bias correction methods are preferable in practice, namely Harrell's bias correction and the .632 and .632+ estimators. Although Harrell's method has been widely adopted in clinical studies, simulation-based evidence indicates that the .632+ estimator may perform better than the other two methods. However, these methods' actual comparative effectiveness is still unclear due to limited numerical evidence. METHODS: We conducted extensive simulation studies to compare the effectiveness of these three bootstrapping methods, particularly using various model building strategies: conventional logistic regression, stepwise variable selections, Firth's penalized likelihood method, ridge, lasso, and elastic-net regression. We generated the simulation data based on the Global Utilization of Streptokinase and Tissue plasminogen activator for Occluded coronary arteries (GUSTO-I) trial Western dataset and considered how event per variable, event fraction, number of candidate predictors, and the regression coefficients of the predictors impacted the performances. The internal validity of C-statistics was evaluated. RESULTS: Under relatively large sample settings (roughly, events per variable ≥ 10), the three bootstrap-based methods were comparable and performed well. However, all three methods had biases under small sample settings, and the directions and sizes of biases were inconsistent. In general, Harrell's and .632 methods had overestimation biases when event fraction become lager. Besides, .632+ method had a slight underestimation bias when event fraction was very small. Although the bias of the .632+ estimator was relatively small, its root mean squared error (RMSE) was comparable or sometimes larger than those of the other two methods, especially for the regularized estimation methods. CONCLUSIONS: In general, the three bootstrap estimators were comparable, but the .632+ estimator performed relatively well under small sample settings, except when the regularized estimation methods are adopted.
BACKGROUND: Multivariable prediction models are important statistical tools for providing synthetic diagnosis and prognostic algorithms based on patients' multiple characteristics. Their apparent measures for predictive accuracy usually have overestimation biases (known as 'optimism') relative to the actual performances for external populations. Existing statistical evidence and guidelines suggest that three bootstrap-based bias correction methods are preferable in practice, namely Harrell's bias correction and the .632 and .632+ estimators. Although Harrell's method has been widely adopted in clinical studies, simulation-based evidence indicates that the .632+ estimator may perform better than the other two methods. However, these methods' actual comparative effectiveness is still unclear due to limited numerical evidence. METHODS: We conducted extensive simulation studies to compare the effectiveness of these three bootstrapping methods, particularly using various model building strategies: conventional logistic regression, stepwise variable selections, Firth's penalized likelihood method, ridge, lasso, and elastic-net regression. We generated the simulation data based on the Global Utilization of Streptokinase and Tissue plasminogen activator for Occluded coronary arteries (GUSTO-I) trial Western dataset and considered how event per variable, event fraction, number of candidate predictors, and the regression coefficients of the predictors impacted the performances. The internal validity of C-statistics was evaluated. RESULTS: Under relatively large sample settings (roughly, events per variable ≥ 10), the three bootstrap-based methods were comparable and performed well. However, all three methods had biases under small sample settings, and the directions and sizes of biases were inconsistent. In general, Harrell's and .632 methods had overestimation biases when event fraction become lager. Besides, .632+ method had a slight underestimation bias when event fraction was very small. Although the bias of the .632+ estimator was relatively small, its root mean squared error (RMSE) was comparable or sometimes larger than those of the other two methods, especially for the regularized estimation methods. CONCLUSIONS: In general, the three bootstrap estimators were comparable, but the .632+ estimator performed relatively well under small sample settings, except when the regularized estimation methods are adopted.
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