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Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000

BACKGROUND: Changes in the geographical distribution of genetic disorders are often thought to happen slowly, especially when compared with infectious diseases. Whereas mutations, genetic drift, and natural selection take place over many generations, epidemics can spread through large populations wi...

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Autores principales: Piel, Frédéric B, Tatem, Andrew J, Huang, Zhuojie, Gupta, Sunetra, Williams, Thomas N, Weatherall, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986033/
https://www.ncbi.nlm.nih.gov/pubmed/24748392
http://dx.doi.org/10.1016/S2214-109X(13)70150-5
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author Piel, Frédéric B
Tatem, Andrew J
Huang, Zhuojie
Gupta, Sunetra
Williams, Thomas N
Weatherall, David J
author_facet Piel, Frédéric B
Tatem, Andrew J
Huang, Zhuojie
Gupta, Sunetra
Williams, Thomas N
Weatherall, David J
author_sort Piel, Frédéric B
collection PubMed
description BACKGROUND: Changes in the geographical distribution of genetic disorders are often thought to happen slowly, especially when compared with infectious diseases. Whereas mutations, genetic drift, and natural selection take place over many generations, epidemics can spread through large populations within a few days or weeks. Nevertheless, population movements can interfere with these processes, and few studies have been done of their effect on genetic disorders. We aimed to investigate the effect of global migration on the distribution of the sickle-cell gene—the most common and clinically significant haemoglobin structural variant. METHODS: For each country, we extracted data from the World Bank's Global Bilateral Migration Database about international human migrations between 1960 and 2000. We combined this information with evidence-based estimates of national HbS allele frequencies, generated within a Bayesian geostatistical framework, to analyse temporal changes in the net numbers of migrants, and classified countries with an index summarising these temporal trends. FINDINGS: The number of international migrants increased from 92·6 million in 1960, to 165·2 million in 2000. The estimated global number of migrants with HbS increased from about 1·6 million in 1960, to 3·6 million in 2000. This increase was largely due to an increase in the number of migrants from countries with HbS allele frequencies higher than 10%, from 3·1 million in 1960, to 14·2 million in 2000. Additionally, the mean number of countries of origin for each destination country increased from 70 (SE 46) in 1960, to 98 (48) in 2000, showing an increasing diversity in the network of international migrations between countries. Our index of change map shows a patchy distribution of the magnitude of temporal changes, with the highest positive and negative values scattered across all continents. INTERPRETATION: Global human population movements have had a substantial effect on the distribution of the HbS gene. Population movements can create a long-term burden on health-care systems. Our findings, which emphasise countries in which migration fluxes are changing the most, should increase awareness about the global burden of haemoglobinopathies and encourage policy makers to implement specific public health interventions, such as screening programmes and genetic counselling. FUNDING: Wellcome Trust, European Research Council, Bill & Melinda Gates Foundation, National Institute of Allergy and Infectious Diseases–National Institutes of Health, the Research and Policy for Infectious Disease Dynamics program, Fogarty International Center.
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spelling pubmed-39860332014-04-17 Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000 Piel, Frédéric B Tatem, Andrew J Huang, Zhuojie Gupta, Sunetra Williams, Thomas N Weatherall, David J Lancet Glob Health Articles BACKGROUND: Changes in the geographical distribution of genetic disorders are often thought to happen slowly, especially when compared with infectious diseases. Whereas mutations, genetic drift, and natural selection take place over many generations, epidemics can spread through large populations within a few days or weeks. Nevertheless, population movements can interfere with these processes, and few studies have been done of their effect on genetic disorders. We aimed to investigate the effect of global migration on the distribution of the sickle-cell gene—the most common and clinically significant haemoglobin structural variant. METHODS: For each country, we extracted data from the World Bank's Global Bilateral Migration Database about international human migrations between 1960 and 2000. We combined this information with evidence-based estimates of national HbS allele frequencies, generated within a Bayesian geostatistical framework, to analyse temporal changes in the net numbers of migrants, and classified countries with an index summarising these temporal trends. FINDINGS: The number of international migrants increased from 92·6 million in 1960, to 165·2 million in 2000. The estimated global number of migrants with HbS increased from about 1·6 million in 1960, to 3·6 million in 2000. This increase was largely due to an increase in the number of migrants from countries with HbS allele frequencies higher than 10%, from 3·1 million in 1960, to 14·2 million in 2000. Additionally, the mean number of countries of origin for each destination country increased from 70 (SE 46) in 1960, to 98 (48) in 2000, showing an increasing diversity in the network of international migrations between countries. Our index of change map shows a patchy distribution of the magnitude of temporal changes, with the highest positive and negative values scattered across all continents. INTERPRETATION: Global human population movements have had a substantial effect on the distribution of the HbS gene. Population movements can create a long-term burden on health-care systems. Our findings, which emphasise countries in which migration fluxes are changing the most, should increase awareness about the global burden of haemoglobinopathies and encourage policy makers to implement specific public health interventions, such as screening programmes and genetic counselling. FUNDING: Wellcome Trust, European Research Council, Bill & Melinda Gates Foundation, National Institute of Allergy and Infectious Diseases–National Institutes of Health, the Research and Policy for Infectious Disease Dynamics program, Fogarty International Center. Elsevier Ltd 2014-02 /pmc/articles/PMC3986033/ /pubmed/24748392 http://dx.doi.org/10.1016/S2214-109X(13)70150-5 Text en © 2014 Piel et al. Open Access article distributed under the terms of CC BY https://creativecommons.org/licenses/by/3.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/3.0/).
spellingShingle Articles
Piel, Frédéric B
Tatem, Andrew J
Huang, Zhuojie
Gupta, Sunetra
Williams, Thomas N
Weatherall, David J
Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
title Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
title_full Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
title_fullStr Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
title_full_unstemmed Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
title_short Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
title_sort global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986033/
https://www.ncbi.nlm.nih.gov/pubmed/24748392
http://dx.doi.org/10.1016/S2214-109X(13)70150-5
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