This report uses structural equation modeling to combine traditional ideas from repeated-measures ANOVA with some traditional ideas from longitudinal factor analysis. A longitudinal model that includes correlations, variances, and means is described as a latent growth curve model (LGM). When merged with repeated-measures data, this technique permits the estimation of parameters representing both individual and group dynamics. The statistical basis of this model allows hypothesis testing of various developmental ideas, including models of alternative dynamic functions and models of the sources of individual differences in these functions. Aspects of these latent growth models are illustrated with a set of longitudinal WISC data from young children and by using the LISREL V computer program.
We compare quantitatively eight stochastic models explaining improvements in mortality rates in England and Wales and in the United States. On the basis of the Bayes Information Criterion (BIC), we find that, for higher ages, an extension of the Cairns-Blake-Dowd (CBD) model that incorporates a cohort effect fits the England and Wales males data best, while for U.S. males data, the Renshaw and Haberman (RH) extension to the Lee and Carter model that also allows for a cohort effect provides the best fit. However, we identify problems with the robustness of parameter estimates under the RH model, calling into question its suitability for forecasting. A different extension to the CBD model that allows not only for a cohort effect, but also for a quadratic age effect, while ranking below the other models in terms of the BIC, exhibits parameter stability across different time periods for both datasets. This model also shows, for both datasets, that there have been approximately linear improvements over time in mortality rates at all ages, but that the improvements have been greater at lower ages than at higher ages, and that there are significant cohort effects.
This paper develops a framework for developing forecasts of future mortality rates. We discuss the suitability of six stochastic mortality models for forecasting future mortality and estimating the density of mortality rates at different ages. In particular, the models are assessed individually with reference to the following qualitative criteria that focus on the plausibility of their forecasts: biological reasonableness; the plausibility of predicted levels of uncertainty in forecasts at different ages; and the robustness of the forecasts relative to the sample period used to fit the model. An important, though unsurprising, conclusion is that a good fit to historical data does not guarantee sensible forecasts. We also discuss the issue of model risk, common to many modelling situations in demography and elsewhere. We find that even for those models satisfying our qualitative criteria, there are significant differences between both central forecasts of mortality rates at different ages and the distributions surrounding those central forecasts.
This paper develops a framework for developing forecasts of future mortality rates. We discuss the suitability of six stochastic mortality models for forecasting future mortality and estimating the density of mortality rates at different ages. In particular, the models are assessed individually with reference to the following qualitative criteria that focus on the plausibility of their forecasts: biological reasonableness; the plausibility of predicted levels of uncertainty in forecasts at different ages; and the robustness of the forecasts relative to the sample period used to fit the model. An important, though unsurprising, conclusion is that a good fit to historical data does not guarantee sensible forecasts. We also discuss the issue of model risk, common to many modelling situations in demography and elsewhere. We find that even for those models satisfying our qualitative criteria, there are significant differences between both central forecasts of mortality rates at different ages and the distributions surrounding those central forecasts.
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