Search arXivSearch

arXiv · 2403.05566

Bringing Age Back In: Accounting for Population Age Distribution in Forecasting Migration

Abstract

The link between age and migration propensity is long established, but existing models of country-level net migration ignore the effect of population age distribution on past and projected migration rates. We propose a method to estimate and forecast international net migration rates for the 200 most populous countries, taking account of changes in population age structure. We use age-standardized estimates of country-level net migration rates and in-migration rates over quinquennial periods from 1990 through 2020 to decompose past net migration rates into in-migration rates and out-migration rates. We then recalculate historic migration rates on a scale that removes the influence of the population age distribution. This is done by scaling past and projected migration rates in terms of a reference population and period. We show that this can be done very simply, using a quantity we call the migration age structure index (MASI). We use a Bayesian hierarchical model to generate joint probabilistic forecasts of total and age- and sex- specific net migration rates over five-year periods for all countries from 2020 through 2100. We find that accounting for population age structure in historic and forecast net migration rates leads to narrower prediction intervals by the end of the century for most countries. Also, applying a Rogers & Castro-like migration age schedule to migration outflows reduces uncertainty in population pyramid forecasts. Finally, accounting for population age structure leads to less out-migration among countries with rapidly aging populations that are forecast to contract most rapidly by the end of the century. This leads to less drastic population declines than are forecast without accounting for population age structure.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Nathan G. Welch, Hana Ševčíková, Adrian E. Raftery. 2024-02-21. Bringing Age Back In: Accounting for Population Age Distribution in Forecasting Migration. https://doi.org/10.1215/00703370-12569854

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Geospatial Foundation Models Capture Health-Relevant Dimensions of Place Beyond Conventional Social Risk Indices

Area-based social risk indices summarize residents' socioeconomic conditions but incompletely capture physical features of place that may affect health. We evaluated whether numerical representations of physical place produced by four geospatial foundation model families from 2022 satellite data explained residual variance in tract-level associations between the Area Deprivation Index, Social Deprivation Index, and Social Vulnerability Index with health outcomes. We used LightGBM to predict variables from the American Community Survey and 40 chronic disease and health-behavior outcomes from CDC PLACES across 82,646 census tracts in the contiguous United States, evaluating performance across 10 held-out states. Among survey variables, models were moderately predictive of some variables including housing type (R-squared up to 0.54) but weak for disability, unemployment, and income disparity. For health outcomes, models explained up to 54% of variance left unexplained by social risk indices, with the largest gains for annual checkups, arthritis, and high blood pressure. Mean total variance explained by geospatial foundation models across the 40 health-related outcomes increased from 0.31 in the smallest tract-size decile to 0.39 in the largest. Geospatial foundation models capture health-relevant features of place not represented by conventional social risk indices and may usefully augment them in epidemiological analyses.

stat.AP

Transporting summary measures of relative effects from randomised trials to the treated patient population: an application to breast cancer endocrine therapy

Randomised trials often report relative treatment effects, such as risk ratios and hazard ratios, for trial populations. Clinical decision-making, however, often benefits from estimates of absolute treatment effects in the population eligible for treatment. Trial participants may not represent this target population well, and restrictions on access to individual participant trial data can further complicate absolute effect estimation. Routine care data are often representative of the target population but may be subject to uncontrolled confounding. We consider estimation of the average treatment effect on the treated (ATT), an absolute measure, by combining a representative sample of treated routine care patients with summary measures (i.e., estimated risk or hazard ratios) from either a randomised trial or a meta-analysis of trials. Under marginal or conditional transportability assumptions, the ATT is shown to be identifiable. The implications of collapsibility of the effect measure on transportability are discussed, and plug-in estimators of the ATT are presented. Simulation studies are used to assess finite sample performance of the estimators in a range of settings. The proposed methods are applied to estimate the ATT of endocrine therapy on 15-year breast cancer mortality using results from a meta-analysis of randomised trials and England's National Disease Registration Service.

stat.AP

Overcoming Model Misspecification in Bayesian Inference of Molecular Signalling Networks

Bayesian inference of molecular signalling networks usually relies on tractability of the marginal likelihood, enabling the set of possible networks to be efficiently explored. As such, linear models with independent errors and conjugate priors are routinely used. However, the dynamics of molecular signalling are nonlinear, and relevant confounders are often unobserved; failure to account for these complexities will almost certainly lead to over-confident inferences in the standard Bayesian framework. To confront this reality, we develop a post-Bayesian approach to inference of molecular signalling networks, guided by the principle that uncertainty should not vanish when the statistical model is misspecified, even in the infinite-data limit. Technically, we extend the predictively-oriented (PrO) posterior of McLatchie et al. (2025) to the setting of latent variable models, empirically investigating the properties of PrO posteriors in the challenging network inference context.

stat.AP