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

被引:116
作者
Piel, Frederic B. [1 ,2 ]
Tatem, Andrew J. [3 ,4 ]
Huang, Zhuojie [5 ,6 ]
Gupta, Sunetra [1 ]
Williams, Thomas N. [2 ,7 ,8 ]
Weatherall, David J. [9 ]
机构
[1] Univ Oxford, Dept Zool, Evolutionary Ecol Infect Dis Grp, Oxford OX1 3PS, England
[2] Global Sickle Cell Dis Network, Toronto, ON, Canada
[3] Univ Southampton, Dept Geog & Environm, Southampton, Hants, England
[4] NIH, Fogarty Int Ctr, Bethesda, MD 20892 USA
[5] Penn State Univ, Ctr Infect Dis Dynam, University Pk, PA 16802 USA
[6] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
[7] Kilifi Dist Hosp, Ctr Geog Med Res Coast, Wellcome Trust Programme, Kenya Med Res Inst, Kilifi, Kenya
[8] Univ London Imperial Coll Sci Technol & Med, St Marys Hosp, Dept Med, London, England
[9] Univ Oxford, Weatherall Inst Mol Med, Oxford, England
来源
LANCET GLOBAL HEALTH | 2014年 / 2卷 / 02期
基金
欧洲研究理事会; 比尔及梅琳达.盖茨基金会; 美国国家卫生研究院; 英国惠康基金;
关键词
CELL-DISEASE; HEALTH BURDEN; S GENE; POPULATION; THALASSEMIA; IMMIGRATION; VARIANTS; EUROPE; EPIDEMIOLOGY; CHALLENGES;
D O I
10.1016/S2214-109X(13)70150-5
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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.
引用
收藏
页码:E80 / E89
页数:10
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