Joint modeling of cross-sectional health outcomes and longitudinal predictors via mixtures of means and variances

Joint modeling methods have become popular tools to link important features extracted from longitudinal data to a primary event. While most modeling strategies have focused on the association between the longitudinal mean trajectories and risk of an event, we consider joint models that incorporate i...

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Bibliographic Details
Published inBiometrics Vol. 71; no. 2; pp. 487 - 497
Main Authors Jiang, Bei, Elliott, Michael R., Sammel, Mary D., Wang, Naisyin
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.06.2015
International Biometric Society
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Summary:Joint modeling methods have become popular tools to link important features extracted from longitudinal data to a primary event. While most modeling strategies have focused on the association between the longitudinal mean trajectories and risk of an event, we consider joint models that incorporate information from both long-term trends and short-term variability in a longitudinal submodel. We also consider both shared random effect and latent class (LC) approaches in the primary-outcome model to predict a binary outcome of interest. We develop simulation studies to compare and contrast these two modeling strategies; in particular, we study in detail the effects of the primary-outcome model misspecification. Among other findings, we note that when we analyze data from a shared random-effect using a LC model while the information from the longitudinal data is weak, the LC approach is more sensitive to such a model misspecification. Under this setting, the LC model has a superior performance in within-sample prediction that cannot be duplicated when predicting new samples. This is a unique feature of the LC approach that is new as far as we know to the existing literature. Finally, we use the proposed models to study how follicle stimulating hormone (FSH) trajectories are related to the risk of developing severe hot flashes for participating women in the Penn Ovarian Aging Study.
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ISSN:0006-341X
1541-0420
DOI:10.1111/biom.12284