4.4 Article

Impact of correlation of predictors on discrimination of risk models in development and external populations

Journal

BMC MEDICAL RESEARCH METHODOLOGY
Volume 17, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12874-017-0345-1

Keywords

AUC; Correlation; External validation; Risk prediction; Simulation study

Funding

  1. NCI Cancer Center Support Grant [P30 CA196521-01]
  2. American Heart Association [16MCPRP31030016]

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Background: The area under the ROC curve (AUC) of risk models is known to be influenced by differences in case-mix and effect size of predictors. The impact of heterogeneity in correlation among predictors has however been under investigated. We sought to evaluate how correlation among predictors affects the AUC in development and external populations. Methods: We simulated hypothetical populations using two different methods based on means, standard deviations, and correlation of two continuous predictors. In the first approach, the distribution and correlation of predictors were assumed for the total population. In the second approach, these parameters were modeled conditional on disease status. In both approaches, multivariable logistic regression models were fitted to predict disease risk in individuals. Each risk model developed in a population was validated in the remaining populations to investigate external validity. Results: For both approaches, we observed that the magnitude of the AUC in the development and external populations depends on the correlation among predictors. Lower AUCs were estimated in scenarios of both strong positive and negative correlation, depending on the direction of predictor effects and the simulation method. However, when adjusted effect sizes of predictors were specified in the opposite directions, increasingly negative correlation consistently improved the AUC. AUCs in external validation populations were higher or lower than in the derivation cohort, even in the presence of similar predictor effects. Conclusions: Discrimination of risk prediction models should be assessed in various external populations with different correlation structures to make better inferences about model generalizability.

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