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How to estimate mortality trends from grouped vital statistics

BACKGROUND: Mortality data at the population level are often aggregated in age classes, for example 5-year age groups with an open-ended interval for the elderly aged 85+. Capturing detailed age-specific mortality patterns and mortality time trends from such coarsely grouped data can be problematic...

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Autores principales: Rizzi, Silvia, Halekoh, Ulrich, Thinggaard, Mikael, Engholm, Gerda, Christensen, Niels, Johannesen, Tom Børge, Lindahl-Jacobsen, Rune
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469310/
https://www.ncbi.nlm.nih.gov/pubmed/30256946
http://dx.doi.org/10.1093/ije/dyy183
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author Rizzi, Silvia
Halekoh, Ulrich
Thinggaard, Mikael
Engholm, Gerda
Christensen, Niels
Johannesen, Tom Børge
Lindahl-Jacobsen, Rune
author_facet Rizzi, Silvia
Halekoh, Ulrich
Thinggaard, Mikael
Engholm, Gerda
Christensen, Niels
Johannesen, Tom Børge
Lindahl-Jacobsen, Rune
author_sort Rizzi, Silvia
collection PubMed
description BACKGROUND: Mortality data at the population level are often aggregated in age classes, for example 5-year age groups with an open-ended interval for the elderly aged 85+. Capturing detailed age-specific mortality patterns and mortality time trends from such coarsely grouped data can be problematic at older ages, especially where open-ended intervals are used. METHODS: We illustrate the penalized composite link model (PCLM) for ungrouping to model cancer mortality surfaces. Smooth age-specific distributions from data grouped in age classes of adjacent calendar years were estimated by constructing a two-dimensional regression, based on B-splines, and maximizing a penalized likelihood. We show the applicability of the proposed model, analysing age-at-death distributions from cancers of all sites in Denmark from 1980 to 2014. Data were retrieved from the Danish Cancer Society and the Human Mortality Database. RESULTS: The main trends captured by PCLM are: (i) a decrease in cancer mortality rates after the 1990s for ages 50–75; (ii) a decrease in cancer mortality in later cohorts for young ages, especially, and very advanced ages. Comparing the raw data by single year of age, with the PCLM-ungrouped distributions, we clearly illustrate that the model fits the data with a high level of accuracy. CONCLUSIONS: The PCLM produces detailed smooth mortality surfaces from death counts observed in coarse age groups with modest assumptions, that is Poisson distributed counts and smoothness of the estimated distribution. Hence, the method has great potential for use within epidemiological research when information is to be gained from aggregated data, because it avoids strict assumptions about the actual distributional shape.
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spelling pubmed-64693102019-04-22 How to estimate mortality trends from grouped vital statistics Rizzi, Silvia Halekoh, Ulrich Thinggaard, Mikael Engholm, Gerda Christensen, Niels Johannesen, Tom Børge Lindahl-Jacobsen, Rune Int J Epidemiol Methods BACKGROUND: Mortality data at the population level are often aggregated in age classes, for example 5-year age groups with an open-ended interval for the elderly aged 85+. Capturing detailed age-specific mortality patterns and mortality time trends from such coarsely grouped data can be problematic at older ages, especially where open-ended intervals are used. METHODS: We illustrate the penalized composite link model (PCLM) for ungrouping to model cancer mortality surfaces. Smooth age-specific distributions from data grouped in age classes of adjacent calendar years were estimated by constructing a two-dimensional regression, based on B-splines, and maximizing a penalized likelihood. We show the applicability of the proposed model, analysing age-at-death distributions from cancers of all sites in Denmark from 1980 to 2014. Data were retrieved from the Danish Cancer Society and the Human Mortality Database. RESULTS: The main trends captured by PCLM are: (i) a decrease in cancer mortality rates after the 1990s for ages 50–75; (ii) a decrease in cancer mortality in later cohorts for young ages, especially, and very advanced ages. Comparing the raw data by single year of age, with the PCLM-ungrouped distributions, we clearly illustrate that the model fits the data with a high level of accuracy. CONCLUSIONS: The PCLM produces detailed smooth mortality surfaces from death counts observed in coarse age groups with modest assumptions, that is Poisson distributed counts and smoothness of the estimated distribution. Hence, the method has great potential for use within epidemiological research when information is to be gained from aggregated data, because it avoids strict assumptions about the actual distributional shape. Oxford University Press 2019-04 2018-09-26 /pmc/articles/PMC6469310/ /pubmed/30256946 http://dx.doi.org/10.1093/ije/dyy183 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods
Rizzi, Silvia
Halekoh, Ulrich
Thinggaard, Mikael
Engholm, Gerda
Christensen, Niels
Johannesen, Tom Børge
Lindahl-Jacobsen, Rune
How to estimate mortality trends from grouped vital statistics
title How to estimate mortality trends from grouped vital statistics
title_full How to estimate mortality trends from grouped vital statistics
title_fullStr How to estimate mortality trends from grouped vital statistics
title_full_unstemmed How to estimate mortality trends from grouped vital statistics
title_short How to estimate mortality trends from grouped vital statistics
title_sort how to estimate mortality trends from grouped vital statistics
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469310/
https://www.ncbi.nlm.nih.gov/pubmed/30256946
http://dx.doi.org/10.1093/ije/dyy183
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