ArticleJournal of the American Statistical Association2023
Time-to-Event Analysis with Unknown Time Origins via Longitudinal Biomarker Registration.
Article in Journal of the American Statistical Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Joint Modeling of Longitudinal and Survival Data in Public Health and Biomedical Research: A Systematic Review.International journal of environmental research and public health · 2026Pooled it
- The Cox-Pólya-Gamma algorithm for flexible Bayesian inference of multilevel survival models.Biometrics · 2025Article
- Estimating Mean Viral Load Trajectory From Intermittent Longitudinal Data and Unknown Time Origins.Statistics in medicine · 2025Article
- Selection of number of clusters and warping penalty in clustering functional electrocardiogram.Statistics in medicine · 2024Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
In observational studies, the time origin of interest for time-to-event analysis is often unknown, such as the time of disease onset. Existing approaches to estimating the time origins are commonly built on extrapolating a parametric longitudinal model, which rely on rigid assumptions that can lead to biased inferences. In this paper, we introduce a flexible semiparametric curve registration model. It assumes the longitudinal trajectories follow a flexible common shape function with person-specific disease progression pattern characterized by a random curve registration function, which is further used to model the unknown time origin as a random start time. This random time is used as a link to jointly model the longitudinal and survival data where the unknown time origins are integrated out in the joint likelihood function, which facilitates unbiased and consistent estimation. Since the disease progression pattern naturally predicts time-to-event, we further propose a new functional survival model using the registration function as a predictor of the time-to-event. The asymptotic consistency and semiparametric efficiency of the proposed models are proved. Simulation studies and two real data applications demonstrate the effectiveness of this new approach.
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Registered trials
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