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Approximating the risk score for disease diagnosis using MARS

机译:使用MARS估算疾病诊断的风险评分

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In disease screening and diagnosis, often multiple markers are measured and combined to improve the accuracy of diagnosis. Mclntosh and Pepe [Combining several screening tests: optimality of the risk score, Biometrics 58 (2002), pp. 657-664] showed that the risk score, defined as the probability of disease conditional on multiple markers, is the optimal function for classification based on the Neyman-Pearson lemma. They proposed a two-step procedure to approximate the risk score. However, the resulting receiver operating characteristic (ROC) curve is only defined in a subrange (L, h) of false-positive rates in (0,1) and the determination of the lower limit L needs extra prior information. In practice, most diagnostic tests are not perfect, and it is usually rare that a single marker is uniformly better than the other tests. Using simulation, I show that multivariate adaptive regression spline is a useful tool to approximate the risk score when combining multiple markers, especially when ROC curves from multiple tests cross. The resulting ROC is defined in the whole range of (0,1) and is easy to implement and has intuitive interpretation. The sample code of the application is shown in the appendix.
机译:在疾病筛查和诊断中,经常会测量和组合多个标记以提高诊断的准确性。 Mclntosh和Pepe [结合几种筛查测试:风险评分的最优性,Biometrics 58(2002),第657-664页]显示,风险评分定义为以多种标记为条件的疾病概率,是分类的最佳功能。基于Neyman-Pearson引理。他们提出了一个两步程序来近似风险评分。但是,仅在(0,1)中的假阳性率的子范围(L,h)中定义所得的接收器工作特性(ROC)曲线,并且确定下限L需要额外的先验信息。实际上,大多数诊断测试都不是完美的,而且通常很少有单个标记要比其他测试统一更好。通过仿真,我证明了当组合多个标记时,尤其是当来自多个测试的ROC曲线交叉时,多元自适应回归样条曲线是一种有用的工具来估算风险得分。生成的ROC定义在(0,1)的整个范围内,易于实现并且具有直观的解释。该应用程序的示例代码在附录中显示。

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