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量化用于竞争风险结局的新型生物标志物的诊断准确性改善情况。

Quantifying diagnostic accuracy improvement of new biomarkers for competing risk outcomes.

作者信息

Wang Zheng, Cheng Yu, Seaberg Eric C, Becker James T

机构信息

Department of Statistics, University of Pittsburgh, Pittsburgh, PA 15260, USA.

Departments of Statistics and Biostatistics, University of Pittsburgh, Pittsburgh, PA 15260, USA

出版信息

Biostatistics. 2020 Feb 21;23(2):666-82. doi: 10.1093/biostatistics/kxaa048.

Abstract

The net reclassification improvement (NRI) and the integrated discrimination improvement (IDI) were originally proposed to characterize accuracy improvement in predicting a binary outcome, when new biomarkers are added to regression models. These two indices have been extended from binary outcomes to multi-categorical and survival outcomes. Working on an AIDS study where the onset of cognitive impairment is competing risk censored by death, we extend the NRI and the IDI to competing risk outcomes, by using cumulative incidence functions to quantify cumulative risks of competing events, and adopting the definitions of the two indices for multi-category outcomes. The "missing" category due to independent censoring is handled through inverse probability weighting. Various competing risk models are considered, such as the Fine and Gray, multistate, and multinomial logistic models. Estimation methods for the NRI and the IDI from competing risk data are presented. The inference for the NRI is constructed based on asymptotic normality of its estimator, and the bias-corrected and accelerated bootstrap procedure is used for the IDI. Simulations demonstrate that the proposed inferential procedures perform very well. The Multicenter AIDS Cohort Study is used to illustrate the practical utility of the extended NRI and IDI for competing risk outcomes.

摘要

净重新分类改善(NRI)和综合判别改善(IDI)最初是为了描述在回归模型中加入新生物标志物时,预测二元结局的准确性改善情况而提出的。这两个指标已从二元结局扩展到多分类和生存结局。在一项艾滋病研究中,认知障碍的发作受到死亡这一竞争风险的审查,我们通过使用累积发病率函数来量化竞争事件的累积风险,并采用多分类结局的两个指标的定义,将NRI和IDI扩展到竞争风险结局。因独立审查导致的“缺失”类别通过逆概率加权来处理。考虑了各种竞争风险模型,如Fine和Gray模型、多状态模型以及多项逻辑模型。给出了从竞争风险数据估计NRI和IDI的方法。基于NRI估计量的渐近正态性构建其推断,对于IDI则使用偏差校正和加速自助程序。模拟表明所提出的推断程序表现良好。多中心艾滋病队列研究用于说明扩展的NRI和IDI在竞争风险结局中的实际效用。

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