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Challenges in modelling the random structure correctly in growth mixture models and the impact this has on model mixtures

Published online by Cambridge University Press:  03 March 2014

M. S. Gilthorpe*
Affiliation:
Division of Epidemiology & Biostatistics, School of Medicine, University of Leeds, Leeds, UK
D. L. Dahly
Affiliation:
Department of Epidemiology and Public Health, University College Cork, Cork, Ireland
Y.-K. Tu
Affiliation:
Institute of Epidemiology & Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan
L. D. Kubzansky
Affiliation:
Department of Social and Behavioral Sciences, Harvard School of Public Health, Boston, MA, USA
E. Goodman
Affiliation:
Mass General Hospital for Children, Department of Pediatrics, Harvard Medical School, Boston, MA, USA
*
*Address for correspondence: M. S. Gilthorpe, Division of Epidemiology & Biostatistics, School of Medicine, University of Leeds, Worsley Building, Clarendon Way, Leeds, LS2 9 LU, UK. (Email m.s.gilthorpe@leeds.ac.uk)
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Abstract

Lifecourse trajectories of clinical or anthropological attributes are useful for identifying how our early-life experiences influence later-life morbidity and mortality. Researchers often use growth mixture models (GMMs) to estimate such phenomena. It is common to place constrains on the random part of the GMM to improve parsimony or to aid convergence, but this can lead to an autoregressive structure that distorts the nature of the mixtures and subsequent model interpretation. This is especially true if changes in the outcome within individuals are gradual compared with the magnitude of differences between individuals. This is not widely appreciated, nor is its impact well understood. Using repeat measures of body mass index (BMI) for 1528 US adolescents, we estimated GMMs that required variance–covariance constraints to attain convergence. We contrasted constrained models with and without an autocorrelation structure to assess the impact this had on the ideal number of latent classes, their size and composition. We also contrasted model options using simulations. When the GMM variance–covariance structure was constrained, a within-class autocorrelation structure emerged. When not modelled explicitly, this led to poorer model fit and models that differed substantially in the ideal number of latent classes, as well as class size and composition. Failure to carefully consider the random structure of data within a GMM framework may lead to erroneous model inferences, especially for outcomes with greater within-person than between-person homogeneity, such as BMI. It is crucial to reflect on the underlying data generation processes when building such models.

Information

Type
Original Article
Creative Commons
Creative Common License - CCCreative Common License - BY
The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution licence http://creativecommons.org/licenses/by/3.0/
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2014
Figure 0

Table 1 Study data set structure and features

Figure 1

Table 2 Summary of growth mixture model (GMM) convergence characteristics and model-fit criteria for the illustrative study data: 10 restricted standard GMMs (Std) and 10 restricted AR1 GMMs (AR1)

Figure 2

Fig. 1 Likelihood-based model-fit criteria for growth mixture models (GMMs): 10 restricted standard (Std) and 10 restricted AR1 (AR1).

Figure 3

Table 3 Contrast of class correspondence based on ordered class sizes for 10 growth mixture models (GMMs) with and without AR1 based on modal assignment of 1528 individuals in the illustrative data set

Figure 4

Fig. 2 Variation in class trajectory intercept residual variances and model trajectory intercept residual variance: 10 restricted standardgrowth mixture models (GMMs; Std) and 10 restricted AR1 GMMs (AR1); for the two-class AR1 model, intercept variance was constrained to zero to attain convergence with non-negative variances.

Figure 5

Table 4 Mean likelihood statistics for growth mixture models (GMMs) of nine simulated data sets

Figure 6

Table 5 Class correspondence for two-class growth mixture models (GMMs): unrestricted random effects and restricted random effects either with or without AR1: mean (s.d.) modal assignments of 1528 individuals across the nine simulated data sets

Supplementary material: PDF

Gilthorpe Supplementary Material

Appendix

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