Discriminant analysis using a multivariate linear mixed model with a normal mixture in the random effects distribution
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
21170920
DOI
10.1002/sim.3849
Knihovny.cz E-resources
- MeSH
- Liver Cirrhosis, Biliary drug therapy MeSH
- Biomarkers analysis MeSH
- Cholagogues and Choleretics therapeutic use MeSH
- Discriminant Analysis * MeSH
- Data Interpretation, Statistical * MeSH
- Ursodeoxycholic Acid therapeutic use MeSH
- Humans MeSH
- Linear Models * MeSH
- Longitudinal Studies MeSH
- Computer Simulation MeSH
- Disease Progression MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Cholagogues and Choleretics MeSH
- Ursodeoxycholic Acid MeSH
We have developed a method to longitudinally classify subjects into two or more prognostic groups using longitudinally observed values of markers related to the prognosis. We assume the availability of a training data set where the subjects' allocation into the prognostic group is known. The proposed method proceeds in two steps as described earlier in the literature. First, multivariate linear mixed models are fitted in each prognostic group from the training data set to model the dependence of markers on time and on possibly other covariates. Second, fitted mixed models are used to develop a discrimination rule for future subjects. Our method improves upon existing approaches by relaxing the normality assumption of random effects in the underlying mixed models. Namely, we assume a heteroscedastic multivariate normal mixture for random effects. Inference is performed in the Bayesian framework using the Markov chain Monte Carlo methodology. Software has been written for the proposed method and it is freely available. The methodology is applied to data from the Dutch Primary Biliary Cirrhosis Study.
References provided by Crossref.org
Dynamic longitudinal discriminant analysis using multiple longitudinal markers of different types
Dynamic classification using credible intervals in longitudinal discriminant analysis