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

机译:全球迁移和镰刀血红蛋白的分布变化:1960年至2000年时间趋势的定量研究

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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. Funding: Wellcome Trust, European Research Council, Bill and 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. © 2014 Piel et al.
机译:背景:人们通常认为遗传性疾病的地理分布变化是缓慢发生的,特别是与传染病相比。突变,遗传漂移和自然选择发生了许多代,而流行病却可以在几天或几周内传播到大批人群中。然而,人口流动会干扰这些过程,关于它们对遗传疾病影响的研究很少。我们旨在研究全球迁移对镰状细胞基因(最常见和临床上最重要的血红蛋白结构变异)分布的影响。方法:对于每个国家,我们从世界银行的全球双边移民数据库中提取有关1960年至2000年之间国际人口迁移的数据。我们将此信息与在贝叶斯地统计学框架内生成的基于证据的国家HbS等位基因频率估计值相结合,以进行分析移民净人数的时间变化,以及分类国家的指数总结了这些时间趋势。调查结果:国际移民的人数从1960年的92·600万增加到2000年的165·200万。估计的全球HbS移民人数从1960年的1·600万增加到2000年的3·600万。这种增加主要是由于来自HbS等位基因频率高于10%的国家的移民人数从1960年的3·100万增加到2000年的14·200万。每个目的国从1960年的70个(东南46)增加到2000年的98个(48),这表明国家之间国际移民网络的多样性在增加。我们的变化指数图显示了时间变化幅度的零星分布,最大正值和负值散布在所有大洲。解释:全球人口迁移对HbS基因的分布产生了重大影响。人口流动会给卫生保健系统带来长期负担。我们的调查结果强调了移民流向变化最大的国家,应该提高人们对全球血红蛋白病负担的认识,并鼓励政策制定者实施特定的公共卫生干预措施,例如筛查计划和基因咨询。资金来源:惠康信托基金,欧洲研究委员会,比尔和梅琳达·盖茨基金会,美国过敏和传染病研究所-国家卫生研究院,传染病动力学研究和政策计划,福格蒂国际中心。 ©2014 Piel等。

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