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首页> 外文期刊>Biometrics: Journal of the Biometric Society : An International Society Devoted to the Mathematical and Statistical Aspects of Biology >Covariate Adjustment in Estimating the Area Under ROC Curve with Partially Missing Gold Standard
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Covariate Adjustment in Estimating the Area Under ROC Curve with Partially Missing Gold Standard

机译:用部分缺失的金标准估计ROC曲线下面积的协变量调整

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摘要

In ROC analysis, covariate adjustment is advocated when the covariates impact the magnitude or accuracy of the test under study. Meanwhile, for many large scale screening tests, the true condition status may be subject to missingness because it is expensive and/or invasive to ascertain the disease status. The complete-case analysis may end up with a biased inference, also known as "verification bias." To address the issue of covariate adjustment with verification bias in ROC analysis, we propose several estimators for the area under the covariate-specific and covariate-adjusted ROC curves (AUCX and AAUC). The AUCT is directly modeled in the form of binary regression, and the estimating equations are based on the U statistics. The AAUC is estimated from the weighted average of AUCa: over the covariate distribution of the diseased subjects. We employ reweighting and imputation techniques to overcome the verification bias problem. Our proposed estimators are initially derived assuming that the true disease status is missing at random (MAR), and then with some modification, the estimators can be extended to the not missing at random (NMAR) situation. The asymptotic distributions are derived for the proposed estimators. The finite sample performance is evaluated by a series of simulation studies. Our method is applied to a data set in Alzheimer's disease research.
机译:在ROC分析中,当协变量影响所研究测试的幅度或准确性时,提倡协变量调整。同时,对于许多大规模的筛查测试,真实状况可能会丢失,因为确定疾病状况的费用昂贵和/或具有侵入性。完整案例分析可能会以有偏差的推理(也称为“验证偏差”)结束。为了解决ROC分析中带有验证偏差的协变量调整问题,我们针对特定于协变量且经协变量调整的ROC曲线下的面积(AUCX和AAUC)提出了几种估算器。 AUCT直接以二元回归的形式建模,估计方程基于U统计量。根据AUCa的加权平均值估算AUC:在患病受试者的协变量分布上。我们采用重新加权和插补技术来克服验证偏差问题。我们最初提出的估计量是在假定真实疾病状态随机(MAR)缺失的情况下得出的,然后通过一些修改,可以将估计量扩展到随机(NMAR)不缺失的情况。为所提出的估计量导出了渐近分布。有限的样品性能通过一系列模拟研究进行评估。我们的方法应用于阿尔茨海默氏病研究中的数据集。

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