Population size estimation in a two-list surveillance system with a discrete covariate

Summary .   Capture–recapture methods are widely adopted to estimate sizes of populations of public health interest using information from surveillance systems. For a two-list surveillance system with a discrete covariate, a population is divided into several subpopulations. A unified framework is proposed in which the logits of presence probabilities are decomposed into case effects and list effects. The estimators for the whole population and subpopulation sizes, their adjusted versions, and asymptotic standard errors admit closed-form expressions. Asymptotic and bootstrap individual and simultaneous confidence intervals are easily constructed. Conditional likelihood ratio tests are used to select one from three possible models. Real examples are investigated.     

Testing and estimation of time-varying cause-specific hazard ratios with covariate adjustment

SUMMARY: In the evaluation of efficacy of a vaccine to protect against disease caused by a genetically diverse infectious pathogen, it is often important to assess whether vaccine protection depends on variations of the exposing pathogen. This problem can be viewed within the framework of a K-competing risks model where the endpoint event is pathogen-specific infection and the cause of failure is the strain type determined after the infection is diagnosed. The Cox model with time-dependent coefficients is used to relate the cause-specific outcomes to explanatory variables to allow for time-varying treatment effects. The strain-specific vaccine efficacy can be defined in terms of one minus the cause-specific hazard ratios. We develop inferential methods for testing whether the vaccine affords some protection against at least one pathogen strain, and for testing equal vaccine protection against the strains, adjusting for covariate effects. We also consider estimation of covariate-adjusted time-varying strain-specific vaccine efficacy. The methods are applied to a dataset from an oral cholera vaccine trial and the performances of the proposed tests are studied through simulations. These techniques apply more generally for testing and estimation of time-varying cause-specific hazard ratios.     

Association Tests for a Censored Quantitative Trait and Candidate Genes in Structured Populations with Multilevel Genetic Relatedness

Summary Several statistical methods for detecting associations between quantitative traits and candidate genes in structured populations have been developed for fully observed phenotypes. However, many experiments are concerned with failure‐time phenotypes, which are usually subject to censoring. In this article, we propose statistical methods for detecting associations between a censored quantitative trait and candidate genes in structured populations with complex multiple levels of genetic relatedness among sampled individuals. The proposed methods correct for continuous population stratification using both population structure variables as covariates and the frailty terms attributable to kinship. The relationship between the time‐at‐onset data and genotypic scores at a candidate marker is modeled via a parametric Weibull frailty accelerated failure time (AFT) model as well as a semiparametric frailty AFT model, where the baseline survival function is flexibly modeled as a mixture of Polya trees centered around a family of Weibull distributions. For both parametric and semiparametric models, the frailties are modeled via an intrinsic Gaussian conditional autoregressive prior distribution with the kinship matrix being the adjacency matrix connecting subjects. Simulation studies and applications to the Arabidopsis thaliana line flowering time data sets demonstrated the advantage of the new proposals over existing approaches.