# Information-theoretic evaluation of covariate distributions models

**Authors:** Niklas Hartung, Aleksandra Khatova

PMC · DOI: 10.1007/s10928-025-09968-5 · Journal of Pharmacokinetics and Pharmacodynamics · 2025-03-27

## TL;DR

This paper evaluates non-Gaussian models for covariate distributions using information theory, showing their advantages over simpler models in life sciences.

## Contribution

A new method for constructing confidence intervals for KL divergence using nearest neighbour estimators and subsampling.

## Key findings

- Non-Gaussian models outperformed Gaussian models in KL divergence across various datasets.
- KL divergence estimates were robust to missing data and latent variables.
- Copula-based models generalized well, while MICE showed overfitting tendencies.

## Abstract

Statistical modelling of covariate distributions allows to generate virtual populations or to impute missing values in a covariate dataset. Covariate distributions typically have non-Gaussian margins and show nonlinear correlation structures, which simple descriptions like multivariate Gaussian distributions fail to represent. Prominent non-Gaussian frameworks for covariate distribution modelling are copula-based models and models based on multiple imputation by chained equations (MICE). While both frameworks have already found applications in the life sciences, a systematic investigation of their goodness-of-fit to the theoretical underlying distribution, indicating strengths and weaknesses under different conditions, is still lacking. To bridge this gap, we thoroughly evaluated covariate distribution models in terms of Kullback–Leibler (KL) divergence, a scale-invariant information-theoretic goodness-of-fit criterion for distributions. Methodologically, we proposed a new approach to construct confidence intervals for KL divergence by combining nearest neighbour-based KL divergence estimators with subsampling-based uncertainty quantification. In relevant data sets of different sizes and dimensionalities with both continuous and discrete covariates, non-Gaussian models showed consistent improvements in KL divergence, compared to simpler Gaussian or scale transform approximations. KL divergence estimates were also robust to the inclusion of latent variables and large fractions of missing values. While good generalization behaviour to new data could be seen in copula-based models, MICE shows a trend for overfitting and its performance should always be evaluated on separate test data. Parametric copula models and MICE were found to scale much better with the dimension of the dataset than nonparametric copula models. These findings corroborate the potential of non-Gaussian models for modelling realistic life science covariate distributions.

## Full-text entities

- **Diseases:** PD (MESH:D010300)
- **Chemicals:** Testosterone (MESH:D013739), cholesterol (MESH:D002784), MICE (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11950120/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC11950120/full.md

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Source: https://tomesphere.com/paper/PMC11950120