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Brad McNeney

Publications and source records attributed to Brad McNeney.

2 recordsLinked to original sources

Log-F-penalized Conditional Logistic Regression for Sparse Data

We investigate penalized likelihood methods for estimation and inference in conditional logistic regression. The standard conditional maximum likelihood estimator is known to be biased away from zero in small or sparse matched case-control studies. A widely used remedy is Firth's penalized likelihood approach, which has good frequentist operating characteristics but provides limited control over the degree of shrinkage applied to individual regression coefficients. We develop point and interval estimators by penalizing the conditional likelihood with independent log-$F$ distributions. The log-\(F\)-penalized approach allows analysts to calibrate shrinkage using interpretable prior assumptions about plausible effect sizes. We also provide practical guidance for calibrating the amount of shrinkage and show that the method can be implemented through data augmentation using standard conditional logistic regression software. We illustrate the methods using data from (i) a study of maternal exposure to diethylstilbestrol and the risk of vaginal cancer in daughters, and (ii) a genetic association study of type 2 diabetes. We then compare the log-$F$-penalized approach with Firth's penalized likelihood method in a simulation study. In simulations, the log-$F$-penalized estimators had confidence-interval coverage comparable to that of Firth's method and lower mean squared error, with similar type~1 error rates and power. These results support the use of log-$F$-penalized conditional logistic regression for inference in sparse matched and stratified studies.

stat.ME↗

The Contribution Plot: Decomposition and Graphical Display of the RV Coefficient, with Application to Genetic and Brain Imaging Biomarkers of Alzheimer's Disease

Alzheimer's disease (AD) is a chronic neurodegenerative disease that causes memory loss and decline in cognitive abilities. AD is the sixth leading cause of death in the United States, affecting an estimated 5 million Americans. To assess the association between multiple genetic variants and multiple measurements of structural changes in the brain a recent study of AD used a multivariate measure of linear dependence, the RV coefficient. The authors decomposed the RV coefficient into contributions from individual variants and displayed these contributions graphically. We investigate the properties of such a `contribution plot' in terms of an underlying linear model, and discuss estimation of the components of the plot when the correlation signal may be sparse. The contribution plot is applied to simulated data and to genomic and brain imaging data from the Alzheimer's Disease Neuroimaging Initiative.

stat.OT↗