A Bayesian approach for mixed effects state‐space models under skewness and heavy tails

Author:

Hernandez‐Velasco Lina L.1ORCID,Abanto‐Valle Carlos A.2,Dey Dipak K.3,Castro Luis M.45ORCID

Affiliation:

1. Facultad de Ciencias Básicas Universidad Santiago de Cali, Calle 5 62‐00 Santiago de Cali Colombia

2. Department of Statistics Federal University of Rio de Janeiro Rio de Janeiro Brazil

3. Department of Statistics University of Connecticut Storrs Connecticut USA

4. Department of Statistics Pontificia Universidad Católica de Chile, Casilla 306, Correo 22 Santiago Chile

5. Center for the Discovery of Structures in Complex Data, Casilla 306, Correo 22 Santiago Chile

Abstract

AbstractHuman immunodeficiency virus (HIV) dynamics have been the focus of epidemiological and biostatistical research during the past decades to understand the progression of acquired immunodeficiency syndrome (AIDS) in the population. Although there are several approaches for modeling HIV dynamics, one of the most popular is based on Gaussian mixed‐effects models because of its simplicity from the implementation and interpretation viewpoints. However, in some situations, Gaussian mixed‐effects models cannot (a) capture serial correlation existing in longitudinal data, (b) deal with missing observations properly, and (c) accommodate skewness and heavy tails frequently presented in patients' profiles. For those cases, mixed‐effects state‐space models (MESSM) become a powerful tool for modeling correlated observations, including HIV dynamics, because of their flexibility in modeling the unobserved states and the observations in a simple way. Consequently, our proposal considers an MESSM where the observations' error distribution is a skew‐t. This new approach is more flexible and can accommodate data sets exhibiting skewness and heavy tails. Under the Bayesian paradigm, an efficient Markov chain Monte Carlo algorithm is implemented. To evaluate the properties of the proposed models, we carried out some exciting simulation studies, including missing data in the generated data sets. Finally, we illustrate our approach with an application in the AIDS Clinical Trial Group Study 315 (ACTG‐315) clinical trial data set.

Publisher

Wiley

Subject

Statistics, Probability and Uncertainty,General Medicine,Statistics and Probability

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