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Time‐to‐event data with time‐varying biomarkers measured only at study entry, with applications to Alzheimer's disease

机译:具有时变生物标志物的延时数据仅在学习进入中测量,具有对阿尔茨海默病的疾病

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Relating time‐varying biomarkers of Alzheimer's disease to time‐to‐event using a Cox model is complicated by the fact that Alzheimer's disease biomarkers are sparsely collected, typically only at study entry; this is problematic since Cox regression with time‐varying covariates requires observation of the covariate process at all failure times. The analysis might be simplified by using study entry as the time origin and treating the time‐varying covariate measured at study entry as a fixed baseline covariate. In this paper, we first derive conditions under which using an incorrect time origin of study entry results in consistent estimation of regression parameters when the time‐varying covariate is continuous and fully observed. We then derive conditions under which treating the time‐varying covariate as fixed at study entry results in consistent estimation. We provide methods for estimating the regression parameter when a functional form can be assumed for the time‐varying biomarker, which is measured only at study entry. We demonstrate our analytical results in a simulation study and apply our methods to data from the Rush Religious Orders Study and Memory and Aging Project and data from the Alzheimer's Disease Neuroimaging Initiative.
机译:与使用COX模型的Alzheimer疾病的时变生物标志物与使用COX模型的时间变化是复杂的,因为阿尔茨海默病生物标志物稀疏收集,通常只在学习条目中;这是有问题的,因为与时变协变量的COX回归需要观察所有失败时的协变化过程。通过使用研究进入作为时间来说,可以简化分析,并在研究进入时测量的时变协变化作为固定基线协变量。在本文中,我们首先推导出在其中使用不正确的研究进入的时间来源的条件导致回归参数的一致估计,当时变调节是连续的并且完全观察到的。然后,我们得到的条件在其处理中,在研究进入的固定过程中导致一致的估计。我们提供用于估计功能形式的回归参数的方法,该时间变化的生物标志物仅在学习条目处测量。我们展示了我们在模拟研究中的分析结果,并将我们的方法应用于来自Ruck宗教订单研究和记忆和老化项目以及阿尔茨海默病神经影像倡议的数据的数据。

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