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Mikko Myrskylä

Publications and source records attributed to Mikko Myrskylä.

2 recordsLinked to original sources

Anticipating Continued Global Fertility Decline via Neural Forecasting

The accelerating shift toward low and ultra-low fertility has intensified the debate over whether countries now undergoing rapid decline are approaching stabilization or entering a more persistent low-fertility regime. Existing projection systems answer that question differently because they embed different assumptions about recovery and about the role of external drivers. To provide an empirical benchmark in this debate, we introduce NeuralTFR, an endogenous global forecasting framework based on a recurrent neural network. Drawing on a harmonized panel of historical fertility series from 196 countries and territories, the model pools cross-country information to learn demographic momentum and generate empirical prediction intervals via multi-quantile regression. Evaluated on a held-out period (2009--2023), NeuralTFR achieves lower point-forecast errors than a Naive Drift baseline and BayesTFR, the United Nations' Bayesian Hierarchical Model, while maintaining competitive uncertainty calibration. In forward projections to 2040, NeuralTFR points to broader exposure to low and very low fertility than BayesTFR, suggesting weaker support for near-term stabilization while still falling short of the most severe decline paths predicted by the Global Burden of Disease project.

stat.AP↗

A demographic scaling model for estimating the total number of COVID-19 infections

Understanding how widely COVID-19 has spread is critical for examining the pandemic's progression. Despite efforts to carefully monitor the pandemic, the number of confirmed cases may underestimate the total number of infections. We introduce a demographic scaling model to estimate COVID-19 infections using an broadly applicable approach that is based on minimal data requirements: COVID-19 related deaths, infection fatality rates (IFRs), and life tables. As many countries lack reliable estimates of age-specific IFRs, we scale IFRs between countries using remaining life expectancy as a marker to account for differences in age structures, health conditions, and medical services. Across 10 countries with most COVID-19 deaths as of May 13, 2020, the number of infections is estimated to be four [95% prediction interval: 2-11] times higher than the number of confirmed cases. Cross-country variation is high. The estimated number of infections is 1.4 million (six times the number of confirmed cases) for Italy; 3.1 million (2.2 times the number of confirmed cases) for the U.S.; and 1.8 times the number of confirmed cases for Germany, where testing has been comparatively extensive. Our prevalence estimates, however, are markedly lower than most others based on local seroprevalence studies. We introduce formulas for quantifying the bias that is required in our data on deaths in order to reproduce estimates published elsewhere. This bias analysis shows that either COVID-19 deaths are severely underestimated, by a factor of two or more; or alternatively, the seroprevalence based results are overestimates and not representative for the total population.

q-bio.PE↗