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

Abstract

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 eff ect on genetic disorders. We aimed to investigate the eff ect 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 eff ect 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.

Figures

Figure 1

Global trends in the number of international migrants and estimated migrants with HbS compared with the 1960s level We calculated the solid red line on the basis of median HbS frequency; the light red area represents the uncertainty on the basis of the 25% and 75% quantiles. HbS=sickle-cell haemoglobin.

Figure 2

Global trends in the average number of countries of origin per country of destination and the average estimated HbS frequency in the countries of origin per country of destination between 1960 and 2000 HbS=sickle-cell haemoglobin.

Figure 3

Estimated net migrations of individuals with HbS at the country level in 1960, 1970, 1980, 1990, and 2000 Countries in red correspond to those in which the estimated number of immigrants with HbS is higher than the estimated number of emigrants with HbS (sink countries). Countries in blue correspond to those in which the estimated number of immigrants with HbS is lower than the estimated number of emigrants with HbS (source countries). To aid comparisons, the same colour classes were used for all maps. HbS=sickle-cell haemoglobin.

Figure 4

Net numbers of migrants and estimated net number of migrants with HbS (based on the posterior median) relative to the 1960 level for selected countries in Africa (A), the Americas (B), Asia (C), and Europe (D), between 1960 and 2000 Countries on the left-hand side tend to be sinks of migrants with HbS (ie, positive values along the y-axis); countries on the right-hand side tend to be sources of migrants with HbS (ie, negative values along the y-axis). Uncertainties (based on the IQR) associated with the trends in migrants with HbS are shown in light red. The appendix shows plots for all countries. HbS=sickle-cell haemoglobin.

Figure 5

Estimated migration fluxes of individuals with HbS from Nigeria between 1960 and 2000 Thickness of the lines is proportional to the estimated number of HbS migrants to a given country. N=estimated number of net migrants with HbS. n=the number of countries to which individuals migrated. HbS=sickle-cell haemoglobin.

Figure 6

Estimated migration fluxes of individuals with HbS to the USA and the UK from 1960 to 2000 The thickness of the lines is proportional to the proportion of HbS migrants from a specific country amongst the total number of HbS immigrants. N=the estimated number of net migrants with HbS. n=the number of countries from which individuals migrated. HbS=sickle-cell haemoglobin.

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