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全球、地区和国家按年龄、性别划分的 240 种死因的全死因和特定死因死亡率,1990-2013 年:2013 年全球疾病负担研究的系统分析。

Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.

出版信息

Lancet. 2015 Jan 10;385(9963):117-71. doi: 10.1016/S0140-6736(14)61682-2. Epub 2014 Dec 18.

Abstract

BACKGROUND

Up-to-date evidence on levels and trends for age-sex-specific all-cause and cause-specific mortality is essential for the formation of global, regional, and national health policies. In the Global Burden of Disease Study 2013 (GBD 2013) we estimated yearly deaths for 188 countries between 1990, and 2013. We used the results to assess whether there is epidemiological convergence across countries.

METHODS

We estimated age-sex-specific all-cause mortality using the GBD 2010 methods with some refinements to improve accuracy applied to an updated database of vital registration, survey, and census data. We generally estimated cause of death as in the GBD 2010. Key improvements included the addition of more recent vital registration data for 72 countries, an updated verbal autopsy literature review, two new and detailed data systems for China, and more detail for Mexico, UK, Turkey, and Russia. We improved statistical models for garbage code redistribution. We used six different modelling strategies across the 240 causes; cause of death ensemble modelling (CODEm) was the dominant strategy for causes with sufficient information. Trends for Alzheimer's disease and other dementias were informed by meta-regression of prevalence studies. For pathogen-specific causes of diarrhoea and lower respiratory infections we used a counterfactual approach. We computed two measures of convergence (inequality) across countries: the average relative difference across all pairs of countries (Gini coefficient) and the average absolute difference across countries. To summarise broad findings, we used multiple decrement life-tables to decompose probabilities of death from birth to exact age 15 years, from exact age 15 years to exact age 50 years, and from exact age 50 years to exact age 75 years, and life expectancy at birth into major causes. For all quantities reported, we computed 95% uncertainty intervals (UIs). We constrained cause-specific fractions within each age-sex-country-year group to sum to all-cause mortality based on draws from the uncertainty distributions.

FINDINGS

Global life expectancy for both sexes increased from 65.3 years (UI 65.0-65.6) in 1990, to 71.5 years (UI 71.0-71.9) in 2013, while the number of deaths increased from 47.5 million (UI 46.8-48.2) to 54.9 million (UI 53.6-56.3) over the same interval. Global progress masked variation by age and sex: for children, average absolute differences between countries decreased but relative differences increased. For women aged 25-39 years and older than 75 years and for men aged 20-49 years and 65 years and older, both absolute and relative differences increased. Decomposition of global and regional life expectancy showed the prominent role of reductions in age-standardised death rates for cardiovascular diseases and cancers in high-income regions, and reductions in child deaths from diarrhoea, lower respiratory infections, and neonatal causes in low-income regions. HIV/AIDS reduced life expectancy in southern sub-Saharan Africa. For most communicable causes of death both numbers of deaths and age-standardised death rates fell whereas for most non-communicable causes, demographic shifts have increased numbers of deaths but decreased age-standardised death rates. Global deaths from injury increased by 10.7%, from 4.3 million deaths in 1990 to 4.8 million in 2013; but age-standardised rates declined over the same period by 21%. For some causes of more than 100,000 deaths per year in 2013, age-standardised death rates increased between 1990 and 2013, including HIV/AIDS, pancreatic cancer, atrial fibrillation and flutter, drug use disorders, diabetes, chronic kidney disease, and sickle-cell anaemias. Diarrhoeal diseases, lower respiratory infections, neonatal causes, and malaria are still in the top five causes of death in children younger than 5 years. The most important pathogens are rotavirus for diarrhoea and pneumococcus for lower respiratory infections. Country-specific probabilities of death over three phases of life were substantially varied between and within regions.

INTERPRETATION

For most countries, the general pattern of reductions in age-sex specific mortality has been associated with a progressive shift towards a larger share of the remaining deaths caused by non-communicable disease and injuries. Assessing epidemiological convergence across countries depends on whether an absolute or relative measure of inequality is used. Nevertheless, age-standardised death rates for seven substantial causes are increasing, suggesting the potential for reversals in some countries. Important gaps exist in the empirical data for cause of death estimates for some countries; for example, no national data for India are available for the past decade.

FUNDING

Bill & Melinda Gates Foundation.

摘要

背景

了解特定年龄-性别全因死亡率和死因死亡率的最新水平和趋势,对于制定全球、区域和国家卫生政策至关重要。在 2013 年全球疾病负担研究(GBD 2013)中,我们估计了 188 个国家 1990 年至 2013 年的每年死亡人数。我们使用这些结果来评估各国之间是否存在流行病学趋同。

方法

我们使用 GBD 2010 方法来估计特定年龄-性别的全因死亡率,并对更新的生命登记、调查和人口普查数据进行了一些改进,以提高准确性。我们通常按照 GBD 2010 的方法来估计死因。关键的改进包括增加了 72 个国家最近的生命登记数据,更新了尸检文献综述,为中国和墨西哥、英国、土耳其和俄罗斯建立了更详细的数据系统。我们改进了垃圾代码重新分配的统计模型。我们使用了 240 种病因中的 6 种不同的建模策略;死因组合建模(CODEm)是具有足够信息的病因的主要策略。阿尔茨海默病和其他痴呆症的趋势是通过对患病率研究进行荟萃回归得出的。对于腹泻和下呼吸道感染的病原体特异性病因,我们使用了反事实方法。我们计算了两种国家间收敛(不平等)的衡量标准:所有国家对之间的平均相对差异(基尼系数)和国家之间的平均绝对差异。为了总结广泛的发现,我们使用多重递降生命表来分解从出生到 15 岁、从 15 岁到 50 岁和从 50 岁到 75 岁以及出生时预期寿命的死亡概率,主要原因。对于报告的所有数量,我们计算了 95%的置信区间(UI)。我们根据不确定性分布的抽样,将每个年龄-性别-国家-年份组内的特定病因比例限制在全因死亡率内。

结果

1990 年至 2013 年期间,全球男女两性的预期寿命从 65.3 岁(UI 65.0-65.6)增加到 71.5 岁(UI 71.0-71.9),而同期的死亡人数从 4750 万(UI 46.8-48.2)增加到 5490 万(UI 53.6-56.3)。全球的进展掩盖了年龄和性别方面的差异:对于儿童,国家之间的平均绝对差异有所减小,但相对差异有所增加。对于 25-39 岁的女性和 75 岁以上的女性,以及 20-49 岁的男性和 65 岁以上的男性,无论是绝对差异还是相对差异都有所增加。全球和区域预期寿命的分解显示,在高收入地区,心血管疾病和癌症的年龄标准化死亡率下降,以及在低收入地区儿童因腹泻、下呼吸道感染和新生儿原因导致的死亡率下降,对预期寿命的影响显著。南部撒哈拉非洲的艾滋病毒/艾滋病降低了预期寿命。对于大多数传染性死因,死亡人数和年龄标准化死亡率都有所下降,而对于大多数非传染性死因,人口结构的变化增加了死亡人数,但降低了年龄标准化死亡率。全球伤害死亡人数增加了 10.7%,从 1990 年的 430 万人增加到 2013 年的 480 万人;但同期年龄标准化率下降了 21%。对于 2013 年每年死亡人数超过 10 万人的一些死因,年龄标准化死亡率在 1990 年至 2013 年期间有所上升,包括艾滋病毒/艾滋病、胰腺癌、心房颤动和扑动、药物使用障碍、糖尿病、慢性肾脏病和镰状细胞贫血。腹泻病、下呼吸道感染、新生儿病因和疟疾仍然是 5 岁以下儿童的前五大死因。轮状病毒是腹泻的主要病原体,肺炎球菌是下呼吸道感染的主要病原体。国家特定的三个生命阶段的死亡概率在国家之间和国家内部都有很大的差异。

解释

对于大多数国家来说,特定年龄-性别的死亡率普遍下降,与非传染性疾病和伤害导致的剩余死亡比例不断增加相一致。评估国家间的流行病学趋同取决于使用绝对或相对不平等衡量标准。然而,七种主要病因的年龄标准化死亡率正在上升,这表明一些国家可能会出现逆转。对于一些国家的死因估计的实证数据存在重要差距;例如,过去十年中印度没有国家数据。

资助

比尔和梅琳达·盖茨基金会。

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