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将半竞争风险数据建模为纵向双变量过程。

Modeling semi-competing risks data as a longitudinal bivariate process.

机构信息

Department of Statistics and Operations Research, Tel Aviv University, Tel Aviv, Israel.

Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.

出版信息

Biometrics. 2022 Sep;78(3):922-936. doi: 10.1111/biom.13480. Epub 2021 May 18.

Abstract

As individuals age, death is a competing risk for Alzheimer's disease (AD) but the reverse is not the case. As such, studies of AD can be placed within the semi-competing risks framework. Central to semi-competing risks, and in contrast to standard competing risks , is that one can learn about the dependence structure between the two events. To-date, however, most methods for semi-competing risks treat dependence as a nuisance and not a potential source of new clinical knowledge. We propose a novel regression-based framework that views the two time-to-event outcomes through the lens of a longitudinal bivariate process on a partition of the time scales of the two events. A key innovation of the framework is that dependence is represented in two distinct forms, local and global dependence, both of which have intuitive clinical interpretations. Estimation and inference are performed via penalized maximum likelihood, and can accommodate right censoring, left truncation, and time-varying covariates. An important consequence of the partitioning of the time scale is that an ambiguity regarding the specific form of the likelihood contribution may arise; a strategy for sensitivity analyses regarding this issue is described. The framework is then used to investigate the role of gender and having ≥1 apolipoprotein E (APOE) ε4 allele on the joint risk of AD and death using data from the Adult Changes in Thought study.

摘要

随着个体年龄的增长,死亡是阿尔茨海默病(AD)的竞争风险,但反之则不然。因此,AD 的研究可以置于半竞争风险框架内。半竞争风险的核心是,与标准竞争风险不同,人们可以了解两个事件之间的依赖结构。然而,迄今为止,大多数半竞争风险方法将依赖视为一种麻烦,而不是潜在的新临床知识来源。我们提出了一种新颖的基于回归的框架,通过将两个事件时间尺度的分区上的纵向双变量过程的视角来看待两个事件时间到事件的结果。该框架的一个关键创新是,依赖以两种不同的形式表示,局部依赖和全局依赖,这两种形式都具有直观的临床解释。估计和推断是通过惩罚最大似然来进行的,可以容纳右删失、左截断和时变协变量。时间尺度分区的一个重要后果是,关于似然贡献的具体形式可能会出现歧义;描述了针对该问题的敏感性分析策略。然后,该框架用于使用来自成人思维变化研究的数据,研究性别和载脂蛋白 E (APOE) ε4 等位基因≥1对 AD 和死亡联合风险的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cf7/11573714/f20daf564623/nihms-2032268-f0001.jpg

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