A Bayesian approach for joint modeling of cluster size and subunit-specific outcomes

被引:78
作者
Dunson, DB
Chen, Z
Harry, J
机构
[1] NIEHS, Biostat Branch, Res Triangle Pk, NC 27709 USA
[2] NIEHS, Mol Toxicol Lab, Res Triangle Pk, NC 27709 USA
关键词
continuation ratio; developmental toxicity; factor analysis; informative cluster size; litter size; multiple outcomes; probit model; random-length data;
D O I
10.1111/1541-0420.00062
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In applications that involve clustered data, such as longitudinal studies and developmental toxicity experiments, the number of subunits within a cluster is often correlated with outcomes measured on the individual subunits. Analyses that ignore this dependency can produce biased inferences. This article proposes a Bayesian framework for jointly modeling cluster size and multiple categorical and continuous outcomes measured on each subunit. We use a continuation ratio probit model for the cluster size and underlying normal regression models for each of the subunit-specific outcomes. Dependency between cluster size and the different outcomes is accommodated through a latent variable structure. The form of the model facilitates posterior computation via a simple and computationally efficient Gibbs sampler. The approach is illustrated with an application to developmental toxicity data, and other applications, to joint modeling of longitudinal and event time data, are discussed.
引用
收藏
页码:521 / 530
页数:10
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