Estimating dengue transmission intensity from serological data: A comparative analysis using mixture and catalytic
Victoria Cox1, Megan O'Driscoll2, Natsuko Imai1
1MRC Centre for Global Infectious Disease Analysis; and the Abdul Latif Jameel Institute for Disease and Emergency Analytics, School of Public Health, Imperial College London, London, United Kingdom.
Plos Neglected Tropical Diseases
|July 11, 2022
Summary
Mixture models offer a less biased approach to estimating dengue virus (DENV) force of infection (FOI) compared to traditional catalytic models. This method is particularly useful for DENV serological data with overlapping antibody distributions.
Area of Science:
- Epidemiology
- Infectious Diseases
- Biostatistics
Background:
- Dengue virus (DENV) infection is a significant global health issue.
- Accurate estimation of the force of infection (FOI) is crucial for effective DENV intervention strategies.
- Traditional catalytic models for DENV FOI estimation rely on antibody thresholds, which can lead to misclassification and biased results.
Purpose of the Study:
- To compare the performance of mixture models against traditional catalytic models (time-constant and time-varying) for estimating DENV FOI.
- To evaluate the application of mixture models using both simulated and real-world serological data.
Main Methods:
- Utilized simulated data to compare bias and coverage of FOI estimates from mixture models and catalytic models.
- Applied mixture models and catalytic models to serological data from Vietnam (2004-2009) and Indonesia (2014).
- Assessed the impact of antibody titre distributions on model performance.
Main Results:
- Simulation studies indicated that mixture models produced less biased FOI estimates compared to catalytic models.
- Both time-varying catalytic and mixture models achieved >95% coverage of the true FOI, with mixture models showing reduced uncertainty.
- Application to Vietnamese data revealed that mixture models often yielded higher FOI and seroprevalence estimates than catalytic models.
Conclusions:
- Mixture models are a valid and potentially less biased alternative to catalytic models for DENV FOI estimation.
- These models are especially beneficial when dealing with serological datasets exhibiting largely overlapping antibody titre distributions.
- The findings support the broader adoption of mixture models in DENV epidemiological research.


