The PX-EM algorithm for fast stable fitting of Henderson's mixed model

This paper presents procedures for implementing the PX-EM algorithm of Liu, Rubin and Wu to compute REML estimates of variance covariance components in Henderson''s linear mixed models. The class of models considered encompasses several correlated random factors having the same vector length e.g., as in random regression models for longitudinal data analysis and in sire-maternal grandsire models for genetic evaluation. Numerical examples are presented to illustrate the procedures. Much better results in terms of convergence characteristics (number of iterations and time required for convergence) are obtained for PX-EM relative to the basic EM algorithm in the random regression.     

Modeling Exposure Intensity and Susceptibility-Latency Effect from Retrospective Cohort Data - Application to Lung Cancer Mortality in Blackfoot Disease Endemic Area in Taiwan

It is challenge in epidemiology to characterize the temperol aspect of exposure-disease association. The authors propose a stochastic model to deal with exposures that are time-dependent and exhibit susceptibility and latency effects. The model is applied to a retrospective cohort data on lung cancer mortality in the blackfoot disease endemic area in Taiwan. The authors compare the proposed model with the multistage model, the back-calculation model, the catalytic model, and the age-period-cohort models.     

Test of marginal compatibility and smoothing methods for exchangeable binary data with unequal cluster sizes

Exchangeable binary data are often collected in developmental toxicity and other studies, and a whole host of parametric distributions for fitting this kind of data have been proposed in the literature. While these distributions can be matched to have the same marginal probability and intra-cluster correlation, they can be quite different in terms of shape and higher-order quantities of interest such as the litter-level risk of having at least one malformed fetus. A sensible alternative is to fit a saturated model (Bowman and George, 1995, Journal of the American Statistical Association 90, 871-879) using the expectation-maximization (EM) algorithm proposed by Stefanescu and Turnbull (2003, Biometrics 59, 18-24). The assumption of compatibility of marginal distributions is often made to link up the distributions for different cluster sizes so that estimation can be based on the combined data. Stefanescu and Turnbull proposed a modified trend test to test this assumption. Their test, however, fails to take into account the variability of an estimated null expectation and as a result leads to inaccurate p-values. This drawback is rectified in this article. When the data are sparse, the probability function estimated using a saturated model can be very jagged and some kind of smoothing is needed. We extend the penalized likelihood method (Simonoff, 1983, Annals of Statistics 11, 208-218) to the present case of unequal cluster sizes and implement the method using an EM-type algorithm. In the presence of covariate, we propose a penalized kernel method that performs smoothing in both the covariate and response space. The proposed methods are illustrated using several data sets and the sampling and robustness properties of the resulting estimators are evaluated by simulations.     

Alternative implementations of Monte Carlo EM algorithms for likelihood inferences

Two methods of computing Monte Carlo estimators of variance components using restricted maximum likelihood via the expectation-maximisation algorithm are reviewed. A third approach is suggested and the performance of the methods is compared using simulated data.     

Mixed effects models with censored data with application to HIV RNA levels

Mixed effects models are often used for estimating fixed effects and variance components in longitudinal studies of continuous data. When the outcome being modelled is a laboratory measurement, however, it may be subject to lower and upper detection limits (i.e., censoring). In this paper, the usual EM estimation procedure for mixed effects models is modified to account for left and/or right censoring.     

A general maximum likelihood analysis of variance components in generalized linear models

This paper describes an EM algorithm for nonparametric maximum likelihood (ML) estimation in generalized linear models with variance component structure. The algorithm provides an alternative analysis to approximate MQL and PQL analyses (McGilchrist and Aisbett, 1991, Biometrical Journal 33, 131-141; Breslow and Clayton, 1993; Journal of the American Statistical Association 88, 9-25; McGilchrist, 1994, Journal of the Royal Statistical Society, Series B 56, 61-69; Goldstein, 1995, Multilevel Statistical Models) and to GEE analyses (Liang and Zeger, 1986, Biometrika 73, 13-22). The algorithm, first given by Hinde and Wood (1987, in Longitudinal Data Analysis, 110-126), is a generalization of that for random effect models for overdispersion in generalized linear models, described in Aitkin (1996, Statistics and Computing 6, 251-262). The algorithm is initially derived as a form of Gaussian quadrature assuming a normal mixing distribution, but with only slight variation it can be used for a completely unknown mixing distribution, giving a straightforward method for the fully nonparametric ML estimation of this distribution. This is of value because the ML estimates of the GLM parameters can be sensitive to the specification of a parametric form for the mixing distribution. The nonparametric analysis can be extended straightforwardly to general random parameter models, with full NPML estimation of the joint distribution of the random parameters. This can produce substantial computational saving compared with full numerical integration over a specified parametric distribution for the random parameters. A simple method is described for obtaining correct standard errors for parameter estimates when using the EM algorithm. Several examples are discussed involving simple variance component and longitudinal models, and small-area estimation.     

Two-component mixture cure rate model with spline estimated nonparametric components

Summary In some survival analysis of medical studies, there are often long-term survivors who can be considered as permanently cured. The goals in these studies are to estimate the noncured probability of the whole population and the hazard rate of the susceptible subpopulation. When covariates are present as often happens in practice, to understand covariate effects on the noncured probability and hazard rate is of equal importance. The existing methods are limited to parametric and semiparametric models. We propose a two-component mixture cure rate model with nonparametric forms for both the cure probability and the hazard rate function. Identifiability of the model is guaranteed by an additive assumption that allows no time-covariate interactions in the logarithm of hazard rate. Estimation is carried out by an expectation-maximization algorithm on maximizing a penalized likelihood. For inferential purpose, we apply the Louis formula to obtain point-wise confidence intervals for noncured probability and hazard rate. Asymptotic convergence rates of our function estimates are established. We then evaluate the proposed method by extensive simulations. We analyze the survival data from a melanoma study and find interesting patterns for this study.