Maximum likelihood estimation in the joint analysis of time‐to‐event and multiple longitudinal variables

Joint modelling of longitudinal and survival data has received much attention in recent years. Most have concentrated on a single longitudinal variable. This paper considers joint modelling in the presence of multiple longitudinal variables. We explore direct association of time‐to‐event and multiple longitudinal processes through a frailty model and use a mixed effects model for each of the longitudinal variables. Correlations among the longitudinal variables are induced through correlated random effects. We allow effects of categorical and continuous covariates on both longitudinal and time‐to‐event responses and explore interactions between the longtudinal variables and other covariates on time‐to‐event. Estimates of the parameters are obtained by maximizing the joint likelihood for the longitudinal variable processes and the event process. We use a one‐step‐late EM algorithm to handle the direct dependence of the event process on the modelled longitudinal variables along with the presence of other fixed covariates in both processes. We argue that such a joint analysis with multiple longitudinal variables is advantageous to one with only a single longitudinal variable in revealing interplay among multiple longitudinal variables and the time‐to‐event. Copyright © 2002 John Wiley & Sons, Ltd.

[1]  M. Wulfsohn,et al.  Modeling the Relationship of Survival to Longitudinal Data Measured with Error. Applications to Survival and CD4 Counts in Patients with AIDS , 1995 .

[2]  M. Palmer Clinical Trials: A Practical Approach , 1985 .

[3]  C. McCulloch,et al.  Latent Class Models for Joint Analysis of Longitudinal Biomarker and Event Process Data , 2002 .

[4]  S L Zeger,et al.  The Evaluation of Multiple Surrogate Endpoints , 2001, Biometrics.

[5]  R Henderson,et al.  Joint modelling of longitudinal measurements and event time data. , 2000, Biostatistics.

[6]  S. Mayne,et al.  Plasma lycopene concentrations in humans are determined by lycopene intake, plasma cholesterol concentrations and selected demographic factors. , 1999, The Journal of nutrition.

[7]  H. Gerster The potential role of lycopene for human health. , 1997, Journal of the American College of Nutrition.

[8]  S. Mayne,et al.  Randomized trial of supplemental beta-carotene to prevent second head and neck cancer. , 2001, Cancer research.

[9]  Richard D. Gill,et al.  A counting process approach to maximum likelihood estimation in frailty models , 1992 .

[10]  M. Davidian,et al.  Estimating the parameters in the Cox model when covariate variables are measured with error. , 1998, Biometrics.

[11]  P. Green On Use of the EM Algorithm for Penalized Likelihood Estimation , 1990 .

[12]  D. Cox Regression Models and Life-Tables , 1972 .

[13]  M. Wulfsohn,et al.  A joint model for survival and longitudinal data measured with error. , 1997, Biometrics.

[14]  Yi Li,et al.  Covariate measurement errors in frailty models for clustered survival data , 2000 .