Title of article :
Parameter Estimation in Longitudinal Studies with Outcome-Dependent Follow-Up
Author/Authors :
Ibrahim، Joseph G. نويسنده , , Fitzmaurice، Garrett M. نويسنده , , Lipsitz، Stuart R. نويسنده , , Gelber، Richard نويسنده , , Lipshultz، Steven نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2002
Pages :
-620
From page :
621
To page :
0
Abstract :
In many observational studies, individuals are measured repeatedly over time, although not necessarily at a set of prespecified occasions. Instead, individuals may be measured at irregular intervals, with those having a history of poorer health outcomes being measured with somewhat greater frequency and regularity; i.e., those individuals with poorer health outcomes may have more frequent follow -up measurements and the intervals between their repeated measurements may be shorter. In this article, we consider estimation of regression parameters in models for longitudinal data where the follow-up times are not fixed by design but can depend on previous outcomes. In particular, we focus on general linear models for longitudinal data where the repeated measures are assumed to have a multivariate Gaussian distribution. We consider assumptions regarding the follow-up time process that result in the likelihood function separating into two components: one for the follow-up time process, the other for the outcome process. The practical implication of this separation is that the former process can be ignored when making likelihood-based inferences about the latter; i.e., maximum likelihood (ML) estimation of the regression parameters relating the mean of the longitudinal outcomes to covariates does not require that a model for the distribution of follow-up times be specified. As a result, standard statistical software, e.g., SAS PROC MIXED (Littell et al., 1996, SAS System for Mixed Models), can be used to analyze the data. However, we also demonstrate that misspecification of the model for the covariance among the repeated measures will, in general, result in regression parameter estimates that are biased. Furthermore, results of a simulation study indicate that the potential bias due to misspecification of the covariance can be quite considerable in this setting. Finally, we illustrate these results using data from a longitudinal observational study (Lipshultz et al., 1995, New England Journal of Medicine332, 1738–1743) that explored the cardiotoxic effects of doxorubicin chemotherapy for the treatment of acute lymphoblastic leukemia in children.
Keywords :
ANALYSIS METHODS , APPLICABILITY , IDENTIFICATION OF CHROMOSOMAL FRAGILE SITES , CHROMOSOMAL FRAGILE SITES
Journal title :
BIOMETRICS (BIOMETRIC SOCIETY)
Serial Year :
2002
Journal title :
BIOMETRICS (BIOMETRIC SOCIETY)
Record number :
84035
Link To Document :
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