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Estimation of log-odds ratio from group testing data using Firth correction
Surupa Roy1, Tathagata Banerjee2
1Department of Statistics, St Xavier's College, Kolkata, India.
Biometrical Journal. Biometrische Zeitschrift
|January 16, 2019
Summary
Estimating rare disease prevalence and log-odds ratios is challenging. Firth correction improves log-odds ratio estimation, and group testing offers more precise results with imperfect diagnostic tests.
Area of Science:
- Biostatistics
- Epidemiology
- Medical Statistics
Background:
- Estimating disease prevalence and group-specific log-odds ratios is crucial for public health.
- Group testing offers a cost-effective approach for disease surveillance, especially for rare conditions.
- Standard estimation methods can be biased, particularly in low-prevalence scenarios.
Purpose of the Study:
- To evaluate methods for estimating rare disease prevalence and log-odds ratios using group testing data.
- To assess the impact of Firth correction on the bias of log-odds ratio estimators.
- To compare the precision of group testing versus individual testing for log-odds ratio estimation with imperfect diagnostic tests.
Main Methods:
- Utilized maximum likelihood estimation for log-odds ratio estimation from group testing data.
- Applied Firth correction to the score function to mitigate bias in estimators.
- Simulated scenarios with low disease prevalence and imperfect diagnostic tests.
Main Results:
- Maximum likelihood estimates of the log-odds ratio are severely biased for low-prevalence diseases.
- Firth correction significantly improves the accuracy of the log-odds ratio estimator.
- Group testing provides more precise log-odds ratio estimates than individual testing when diagnostic tests are imperfect.
Conclusions:
- Firth correction is a valuable technique for reducing bias in log-odds ratio estimation from group testing data, especially for rare diseases.
- Group testing, even with imperfect diagnostics, can be more efficient than individual testing for estimating group differences in disease risk.
- These findings have implications for optimizing surveillance strategies for rare diseases.
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