ArticleStatistical methods in medical research2026
A joint model for a longitudinal outcome and a progressive multistate model under a mixed observation scheme.
Article in Statistical methods in medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Joint models for longitudinal and event-time data can be used to understand the co-development of multiple correlated non-fatal outcomes, such as those encountered when studying diabetic microvascular complications. However, such models were not developed for event-times characterized by a multistate process where the entry time into certain states is interval-censored, which is an important feature of interval cohort study designs. Our aim was to develop a joint model for this setting. Specifically, we formulated a shared random effects joint model with linear mixed-effects and proportional intensities progressive three-state Markov submodels, with interval-censoring of entry into the transient state and exact observation of entry into the absorbing state. Maximum likelihood estimation was used, with exploration of the functional forms and association structures. Bias and confidence interval coverage of the model parameters were assessed using simulation, and performance was compared to existing approaches that assume exact observation of all entry times, which were found to sometimes overestimate the magnitude of association between the longitudinal and multistate outcomes. In an application of the model, the trajectory of a routinely measured diabetic complication (retinopathy) was associated with progression through states of a more difficult to measure complication (neuropathy), suggesting potential efficiencies in screening and monitoring.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.