Evidence map›Paper›PMID 37771511›Full record

ArticleJournal of the American Statistical Association2023

Time-to-Event Analysis with Unknown Time Origins via Longitudinal Biomarker Registration.

Tianhao Wang, Sarah J Ratcliffe, Wensheng Guo

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Tianhao WangDepartment of Neurological Sciences, and Faculty Statistician, Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL 60612.
Sarah J RatcliffeDivision of Biostatistics, Department of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, VA 22908.
Wensheng GuoDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.

Funding

Dynamic Longitudinal Functional Models with Applications to the CRIC StudyR01HL161303 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI DEO, RAJAT, GUO, WENSHENG · 2022 to 2025
$2.8M
Early detection, containment, and management of COVID-19 in dialysis facilities using multi-modal data sourcesR01DK130067 · NIDDK · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI GUO, WENSHENG, KOTANKO, PETER · 2021 to 2023
$2.0M
Semi-Parametric Subgroup Analysis for Longitudinal Data with Applications to Multidisciplinary Approach to the Study of Chronic Pelvic Pain (MAPP) StudyR01DK117208 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GUO, WENSHENG · 2019 to 2022
$1.5M
Semi-parametric joint models for longitudinal and time to event dataR01GM104470 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GUO, WENSHENG, RATCLIFFE, SARAH J · 2013 to 2016
$1.2M
NHLBI NIH HHS R01 HL161303NIDDK NIH HHS R01 DK117208NIDDK NIH HHS R01 DK130067NIGMS NIH HHS R01 GM104470
6 · The paper itself

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.

Indexed as

accelerated failure timecurve registrationjoint modelingleft censoringsieve estimation

Identifiers

PMID37771511
PMCPMC10530746

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.