SearcharxivSearch

arXiv · 2504.15150

Prevalence estimation in infectious diseases with imperfect tests: A comparison of Frequentist and Bayesian Logistic Regression methods with misclassification correction

Abstract

Accurate estimation of disease prevalence is essential for guiding public health strategies. Imperfect diagnostic tests can cause misclassification errors-false positives (FP) and false negatives (FN)-that may skew estimates if unaddressed. This study compared four statistical methods for estimating the prevalence of sexually transmitted infections (STIs) and associated factors, while correcting for misclassification. The methods were: (1) Standard Logistic Regression with external correction using known sensitivity and specificity; (2) the Liu et al. model, which jointly estimates FP and FN rates; (3) Bayesian Logistic Regression with external correction; and (4) a Bayesian model with internal correction using informative priors on diagnostic accuracy. Data came from 11,452 participants in a voluntary screening campaign for HIV, syphilis, and hepatitis B (2020-2024). Prevalence estimates and regression coefficients were compared across models using relative changes from crude estimates, confidence interval (CI) width, and coefficient variability. The Liu model produced higher prevalence estimates but had wider CIs and convergence issues in low-prevalence settings. The Bayesian model with internal correction gave intermediate estimates with the narrowest CIs and more stable intercepts, suggesting improved baseline prevalence estimation. Informative or weakly informative priors helped regularize estimates, especially in small-sample or rare-event contexts. Accounting for misclassification influenced both prevalence and covariate associations. While the Liu model offers theoretical strengths, its practical limitations in sparse data settings reduce its utility. Bayesian models with misclassification correction emerge as robust and flexible tools, particularly valuable in low-prevalence contexts where diagnostic uncertainty is high.

Explore related subjects

Keep this discovery

BibTeXRIS

Jorge Mario Estrada Alvarez, Henan F. Garcia, Miguel Ángel Montero-Alonso, Juan de Dios Luna del Castillo. 2025-04-18. Prevalence estimation in infectious diseases with imperfect tests: A comparison of Frequentist and Bayesian Logistic Regression methods with misclassification correction. https://arxiv.org/abs/2504.15150

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Surprise Reduction and Nullification in Bayesian and Inverse Bayesian Inference under Ambiguous Prediction-Error Attribution

In non-stationary environments, prediction errors may signal environmental change or transient outliers, and adaptive systems must track such changes without overreacting to outliers. We distinguish surprise reduction, which updates beliefs to fit observations, from surprise nullification, which weakens constraints imposed by the predictive structure, and formalize both within Bayesian and inverse Bayesian (BIB) inference. Belief and likelihood updates are derived from variational objectives sharing a nullification strength, determined endogenously by minimizing surprise under the candidate post-update predictive distribution. In the Gaussian case, nullification expands belief and likelihood variances by a common factor relative to standard Bayesian updating, leaving the ratio unchanged. BIB thus defers attribution of the prediction error, committing to neither latent-state change nor observation-process uncertainty. The nullification strength is carried over as a candidate and is maintained or released according to the predictive surprise of the next observation. In a mean estimation task with outliers and changepoints, no scanned parameter setting of a Sage-Husa-type adaptive Kalman filter, fixed-strength BIB variant, or belief-forgetting-only variant outperforms BIB in both changepoint tracking and post-outlier stability. An oracle-informed reduced Bayesian model tracks changepoints better but is less stable after outliers. Although BIB maintains no explicit hypotheses about changepoints or outliers, it generates event-dependent dynamics. The learning rate increases after changepoints, whereas after outliers, nullification is released, and this increase is suppressed. Deferring attribution and letting subsequent observations differentiate the responses may constitute a principle of adaptive inference in non-stationary environments.

stat.ME

Generalized Ridge Refitting for the Lasso and Prediction Improvement Bounds

We study a class of Lasso based estimators obtained by applying a quadratic correction on the Lasso equicorrelation set. The penalty matrix determines both the magnitude and geometry of the correction and contains, among other cases, the isotropic Lasso--Ridge correction, least squares refitting, Gram proportional interpolation between the Lasso and least squares, and coordinate specific penalties. We first derive a closed form representation and isolate the positive gain component of the resulting prediction improvement. We then control the remaining stochastic linear term in expectation by localizing the random signed equicorrelation model around a deterministic reference support. This yields a finite sample expectation bound that explicitly accounts for the randomness induced by Lasso model selection. The resulting decomposition provides a unified framework for understanding when Lasso based quadratic corrections can improve prediction.

stat.ME

Discretization in covariate-adaptive randomization: gains and losses

Covariate-adaptive randomization(CAR) is widely implemented in clinical trials to balance prognostic covariates across treatment arms. Continuous covariates are often discretized into strata in practice, yet their consequences are not clearly understood. This paper provides a comprehensive study of the impact of discretization on both the CAR design process and the inferential results thereafter. We establish the asymptotic properties of both imbalance measures and treatment effect estimators under discretized and non-discretized settings. Practical recommendations are given on when and how discretization should be employed. We show that discretization in design is generally recommended, as it enhances robustness against model misspecification. However, if the true model is known, the most efficient strategy is to balance covariates according to that model in the design. The theoretical results are corroborated by extensive simulation studies and an empirical application to a diabetes trial dataset. Together, the results clarify the gains and losses of discretization in CAR and pave the way for learning impact of discretization to other designs and beyond.

stat.ME