A Bayesian location-scale joint model for time-to-event and multivariate longitudinal data with association based on within-individual variability

Within-individual variability of health indicators measured over time is becoming commonly used to inform about disease progression. Simple summary statistics (e.g. the standard deviation for each individual) are often used but they are not suited to account for time changes. In addition, when these summary statistics are used as covariates in a regression model for time-to-event outcomes, the estimates of the hazard ratios are subject to regression dilution. To overcome these issues, a joint model is built where the association between the time-to-event outcome and multivariate longitudinal markers is specified in terms of the within-individual variability of the latter. A mixed-effect location-scale model is used to analyse the longitudinal biomarkers, their within individual variability and their correlation. The time to event is modelled using a proportional hazard regression model, with a flexible specification of the baseline hazard, and the information from the longitudinal biomarkers is shared as a function of the random effects. The model can be used to quantify within-individual variability for the longitudinal markers and their association with the time-to-event outcome. We show through a simulation study the performance of the model in comparison with standard joint models with constant variance. The model is applied on a dataset of adult women from the UK cystic fibrosis registry, to evaluate the association between lung function, malnutrition and mortality.

Authors

Publication Details

Journal
Apollo (University of Cambridge)
Published
2026-05-08
DOI
https://doi.org/10.17863/cam.129980
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
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article

A Bayesian location-scale joint model for time-to-event and multivariate longitudinal data with association based on within-individual variability

David Taylor-Robinson, Marco A. Palma, Siobhán B Carr, Rhonda Szczesniak et al.
Apollo (University of Cambridge)
Cystic Fibrosis Research Advances
article

A Bayesian location-scale joint model for time-to-event and multivariate longitudinal data with association based on within-individual variability

David Taylor-Robinson, Marco A. Palma, Siobhán B Carr, Rhonda Szczesniak, Omar El Makkaoui, Graciela Muniz-Terrera, Jessica Barrett, Angela Wood, Ruth H Keogh
article en

Abstract

Within-individual variability of health indicators measured over time is becoming commonly used to inform about disease progression. Simple summary statistics (e.g. the standard deviation for each individual) are often used but they are not suited to account for time changes. In addition, when these summary statistics are used as covariates in a regression model for time-to-event outcomes, the estimates of the hazard ratios are subject to regression dilution. To overcome these issues, a joint model is built where the association between the time-to-event outcome and multivariate longitudinal markers is specified in terms of the within-individual variability of the latter. A mixed-effect location-scale model is used to analyse the longitudinal biomarkers, their within individual variability and their correlation. The time to event is modelled using a proportional hazard regression model, with a flexible specification of the baseline hazard, and the information from the longitudinal biomarkers is shared as a function of the random effects. The model can be used to quantify within-individual variability for the longitudinal markers and their association with the time-to-event outcome. We show through a simulation study the performance of the model in comparison with standard joint models with constant variance. The model is applied on a dataset of adult women from the UK cystic fibrosis registry, to evaluate the association between lung function, malnutrition and mortality.

Apollo (University of Cambridge)
Zero hunger
Openalex Percentile: Top 5%
Cystic Fibrosis Research Advances
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