A high-dimensional joint model for longitudinal outcomes of different nature

被引:27
作者
Faes, Christel [1 ]
Aerts, Marc [1 ]
Molenberghs, Geert [1 ]
Geys, Helena [2 ]
Teuns, Greet [2 ]
Bijnens, Luc [2 ]
机构
[1] Hasselt Univ, Ctr Stat, Diepenbeek, Belgium
[2] Johnson & Johnson, PRD Biometr & Clin Informat, Beerse, Belgium
关键词
mixed outcomes; high-dimensional joint model; pseudo-likelihood; longitudinal data;
D O I
10.1002/sim.3314
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In repeated dose-toxicity studies, many outcomes are repeatedly measured on the same animal to study the toxicity of a compound of interest. This is only one example in which one is confronted with the analysis of many outcomes, possibly of a different type. Probably the most common situation is that of an amalgamation of continuous and categorical outcomes. A possible approach towards the joint analysis of two longitudinal outcomes of a different nature is the use of random-effects models (Models for Discrete Longitudinal Data. Springer Series in Statistics. Springer: New York, 2005). Although a random-effects model can easily be extended to jointly model many outcomes of a different nature, computational problems arise as the number of outcomes increases. To avoid maximization of the full likelihood expression, Fieuws and Verbeke (Biometrics 2006; 62:424-431) proposed a pairwise modeling strategy in which all possible pairs are modeled separately, using a mixed model, yielding several different estimates for the same parameters. These latter estimates are then combined into a single set of estimates. Also inference, based on pseudo-likelihood principles, is indirectly derived from the separate analyses. In this paper, we extend the approach of Fieuws and Verbeke (Biometrics 2006; 62:424-431) in two ways: the method is applied to different types of outcomes and the full pseudo-likelihood expression is maximized at once, leading directly to unique estimates as well as direct application of pseudo-likelihood inference. This is very appealing when interested in hypothesis testing. The method is applied to data from a repeated dose-toxicity study designed for the evaluation of the neurofunctional effects of a psychotrophic drug. The relative merits of both methods are discussed. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:4408 / 4427
页数:20
相关论文
共 25 条
[1]  
Aerts M., 2002, Topics in Modelling of Clustered Data, DOI DOI 10.1201/9781420035889
[2]  
[Anonymous], 2002, ANAL LONGITUDINAL DA
[3]  
ARNOLD BC, 1991, SANKHYA SER B, V53, P233
[4]   BIVARIATE LATENT VARIABLE MODELS FOR CLUSTERED DISCRETE AND CONTINUOUS OUTCOMES [J].
CATALANO, PJ ;
RYAN, LM .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1992, 87 (419) :651-658
[5]  
COX DR, 1992, BIOMETRIKA, V79, P441, DOI 10.1093/biomet/79.3.441
[6]  
COX DR, 1994, BIOMETRIKA, V81, P403, DOI 10.2307/2336971
[7]   Modeling combined continuous and ordinal outcomes in a clustered setting [J].
Faes, C ;
Geys, H ;
Aerts, M ;
Molenberghs, G ;
Catalano, PJ .
JOURNAL OF AGRICULTURAL BIOLOGICAL AND ENVIRONMENTAL STATISTICS, 2004, 9 (04) :515-530
[8]   Pairwise fitting of mixed models for the joint modeling of multivariate longitudinal profiles [J].
Fieuws, S ;
Verbeke, G .
BIOMETRICS, 2006, 62 (02) :424-431
[9]   Pseudo-likelihood inference for clustered binary data [J].
Geys, H ;
Molenberghs, G ;
Ryan, LM .
COMMUNICATIONS IN STATISTICS-THEORY AND METHODS, 1997, 26 (11) :2743-2767
[10]   Two latent variable risk assessment approaches for mixed continuous and discrete outcomes from developmental toxicity data [J].
Geys, H ;
Regan, MM ;
Catalano, PJ ;
Molenberghs, G .
JOURNAL OF AGRICULTURAL BIOLOGICAL AND ENVIRONMENTAL STATISTICS, 2001, 6 (03) :340-355