Joint Spatial Modeling of Recurrent Infection and Growth with Processes Under Intermittent Observation

In this article we present new statistical methodology for longitudinal studies in forestry where trees are subject to recurrent infection and the hazard of infection depends on tree growth over time. Understanding the nature of this dependence has important implications for reforestation and breeding programs. Challenges arise for statistical analysis in this setting with sampling schemes leading to panel data, exhibiting dynamic spatial variability, and incomplete covariate histories for hazard regression. In addition, data are collected at a large number of locations which poses computational difficulties for spatiotemporal modeling. A joint model for infection and growth is developed; wherein, a mixed non-homogeneous Poisson process, governing recurring infection, is linked with a spatially dynamic nonlinear model representing the underlying height growth trajectories. These trajectories are based on the von Bertalanffy growth model and a spatially-varying parametrization is employed. Spatial variability in growth parameters is modeled through a multivariate spatial process derived through kernel convolution. Inference is conducted in a Bayesian framework with implementation based on hybrid Monte Carlo. Our methodology is applied for analysis in an eleven year study of recurrent weevil infestation of white spruce in British Columbia

Assessing noninferiority in a three-arm trial using the Bayesian Approach

Non-inferiority trials, which aim to demonstrate that a test product is not worse than a competitor by more than a pre-specified small amount, are of great importance to the pharmaceutical community. As a result, methodology for designing and analyzing such trials is required, and developing new methods for such analysis is an important area of statistical research. The three-arm clinical trial is usually recommended for non-inferiority trials by the Food and Drug Administration (FDA). The three-arm trial consists of a placebo, a reference, and an experimental treatment, and simultaneously tests the superiority of the reference over the placebo along with comparing this reference to an experimental treatment. In this paper, we consider the analysis of noninferiority trials using Bayesian methods which incorporate both parametric as well as semi-parametric models. The resulting testing approach is both flexible and robust. The benefit of the proposed Bayesian methods is assessed via simulation, based on a study examining Home Based Blood Pressure Interventions