跳到正文
← 返回论文列表与筛选
阅读说明

本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要聚焦临床纵向标志物与生存时间的联合建模,未明确对应所列计量领域细分。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Yan Wang
Jeremy M. G Taylor

纵向数据与事件时间数据的联合建模:艾滋病应用

研究问题
定期测量的疾病标志物如何与发病时间联合分析,并在估计标志物和基线协变量的风险关联时处理测量误差?
方法与思路
作者结合含随机截距、积分 Ornstein–Uhlenbeck 过程和测量误差的纵向模型与比例风险模型,并用 MCMC 拟合。
材料陈述的贡献
摘要称,联合估计可同时刻画基线变量与 CD4 变化的关联,以及当前 CD4 与发病风险的关联,并将测量误差纳入风险模型。
阅读关注点
应核对纵向过程与风险模型如何连接、事件过程与测量误差的假设,以及模拟中联合建模和分别建模的比较设计。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明;摘要未说明完整模型条件、模拟数值及计算诊断,风险关联不能直接解释为因果效应。

原文摘要

In many clinical and epidemiologic studies, periodically measured disease markers are used to monitor progression to the onset of disease. Motivated by a study of CD4 counts in men infected with human immunodeficiency virus (HIV) at risk for acquired immunodeficiency syndrome (AIDS), we developed a joint model for analysis of both longitudinal and event time data. We use a longitudinal model for continuous data that incorporates a mean structure dependent on covariates, a random intercept, a stochastic process, and measurement error. A central component of the longitudinal model is an integrated Ornstein–Uhlenbeck stochastic process, which represents a family of covariance structures with a random effects model and Brownian motion as special cases. The regression model for the event time data is a proportional hazards model that includes the longitudinal marker as a time-dependent variable and other covariates. A Markov chain Monte Carlo algorithm was developed for fitting the joint model. The joint modeling approach is evaluated and compared with the approach of separate modeling through simulation studies, and it is applied to CD4 counts and AIDS event time data from a cohort study of HIV-infected men. The joint estimation approach allows the simultaneous estimation of the effect of baseline covariates on the progression of CD4 counts and the effect of the current CD4 count and baseline covariates on the hazard of AIDS. The joint modeling approach also gives a way to incorporate measurement error in CD4 counts into a hazard model.

笔记与分组