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Mediation Analysis in Bayesian Extended Redundancy Analysis with Mixed Outcome Variables

Published online by Cambridge University Press:  03 January 2025

Ji Yeh Choi
Affiliation:
Department of Psychology, York University, 4700 Keele St., Toronto, ON, Canada
Minjung Kyung
Affiliation:
Department of Statistics, Duksung Women’s University, 33 Samyang-ro, 144-gil, Dobong-gu, Seoul, Republic of Korea
Ju-Hyun Park*
Affiliation:
Department of Statistics, Dongguk University, 30 Phildong-ro 1-gil, Jung-gu, Seoul, Republic of Korea
*
Corresponding author: Ju-Hyun Park; Email: juhyunp@dongguk.edu.
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Abstract

Extended redundancy analysis (ERA) is a statistical approach to component-based multivariate regression modeling that explores interrelationships among multiple sets of while incorporating regression with a data-reduction technique. The extant models that utilize ERA have assumed the outcome variables with the same data type. Also, ERA models focused on estimating direct pathways only without explicitly addressing mediation effects. In this paper, ERA is extended to handle multiple mediators and mixed types of outcome variables by adopting a Bayesian framework, taking into account correlation structure among all of the outcome variables. The proposed method develops an algorithm that derives the joint posterior distribution of parameters using a Markov chain Monte Carlo algorithm. Simulations and an empirical dataset are provided to illustrate the usefulness of the proposed method.

Information

Type
Theory and Methods
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of Psychometric Society
Figure 0

Figure 1 MCMC algorithm to update parameters from the posterior distribution.

Figure 1

Figure 2 A hypothesized model for the first simulation study (with one continuous and two ordinal outcome variables).

Figure 2

Figure 3 Trace plots of selected parameters for the simulation study with N = 100.

Figure 3

Table 1 Results of the simulation study varying sample sizes (N = 100, 300, 500)

Figure 4

Table 2 Results of indirect effect estimates obtained from the simulation study varying across sample sizes

Figure 5

Table 3 Results of total effect estimates without the mediators from the simulation study varying across sample sizes

Figure 6

Figure 4 A hypothesized model for the empirical data.

Figure 7

Figure 5 Trace plots of selected parameters for the empirical data.

Figure 8

Table 4 Results of fitting the National Survey on Drug Use and Health (NSDUH) data

Figure 9

Table 5 Results of indirect effect estimates obtained from the empirical NSDUH data