Joint modeling of longitudinal and survival data with a covariate subject to a limit of detection

We develop and study an innovative method for jointly modeling longitudinal response and time-to-event data with a covariate subject to a limit of detection. The joint model assumes a latent process based on random effects to describe the association between longitudinal and time-to-event data. We study the role of the association parameter on the regression parameters estimators. We model the longitudinal and survival outcomes using linear mixed-effects and Weibull frailty models, respectively. Because of the limit of detection, missing covariate (explanatory variable, x) values may lead to the non-ignorable missing, resulting in biased parameter estimates with poor coverage probabilities of the confidence interval. We define and estimate the probability of missing due to the limit of detection. Then we develop a novel joint density and hence the likelihood function that incorporates the effect of left-censored covariate. Monte Carlo simulations show that the estimators of the proposed method are approximately unbiased and provide expected coverage probabilities for both longitudinal and survival submodels parameters. We also present an application of the proposed method using a large clinical dataset of pneumonia patients obtained from the Genetic and Inflammatory Markers of Sepsis study.

[1]  Abdus Sattar,et al.  A Parametric Survival Model When a Covariate is Subject to Left-Censoring. , 2012, Journal of biometrics & biostatistics.

[2]  Joseph G Ibrahim,et al.  Joint modeling of survival and longitudinal non‐survival data: current methods and issues. Report of the DIA Bayesian joint modeling working group , 2015, Statistics in medicine.

[3]  Geert Molenberghs,et al.  Joint models for longitudinal data: Introduction and overview , 2008 .

[4]  Frailty models for pneumonia to death with a left‐censored covariate , 2015, Statistics in medicine.

[5]  C. McCulloch Maximum Likelihood Algorithms for Generalized Linear Mixed Models , 1997 .

[6]  Joseph G Ibrahim,et al.  Basic concepts and methods for joint models of longitudinal and survival data. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[7]  Wei Shen,et al.  Assessing model fit in joint models of longitudinal and survival data with applications to cancer clinical trials , 2014, Statistics in medicine.

[8]  Joseph G Ibrahim,et al.  Sample size and power determination in joint modeling of longitudinal and survival data , 2011, Statistics in medicine.

[9]  John A Kellum,et al.  Understanding the inflammatory cytokine response in pneumonia and sepsis: results of the Genetic and Inflammatory Markers of Sepsis (GenIMS) Study. , 2007, Archives of internal medicine.

[10]  Rizopoulos Dimitris,et al.  Joint Modeling of Longitudinal and Time-to-Event Data , 2014 .

[11]  Lang Wu,et al.  Mixed Effects Models for Complex Data , 2019 .

[12]  Peter J. Diggle,et al.  Random effects models for joint analysis of repeated measurement and time-to-event outcomes , 2008 .

[13]  Geert Molenberghs,et al.  Analysis of non‐ignorable missing and left‐censored longitudinal data using a weighted random effects tobit model , 2011, Statistics in medicine.

[14]  M. Unruh,et al.  Joint Modeling of All-Cause Mortality and Longitudinally Measured Serum Albumin , 2012 .

[15]  Gang Li,et al.  Joint Modeling of Longitudinal and Time-to-Event Data , 2016 .

[16]  J. Ware,et al.  Random-effects models for longitudinal data. , 1982, Biometrics.

[17]  Keith R. Abrams,et al.  Joint Modeling of Longitudinal and Survival Data , 2013 .