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2019 年与 85 种病原体相关的全球负担:2019 年全球疾病负担研究的系统分析。

Global burden associated with 85 pathogens in 2019: a systematic analysis for the Global Burden of Disease Study 2019.

出版信息

Lancet Infect Dis. 2024 Aug;24(8):868-895. doi: 10.1016/S1473-3099(24)00158-0. Epub 2024 Apr 16.

DOI:10.1016/S1473-3099(24)00158-0
PMID:38640940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11269650/
Abstract

BACKGROUND

Despite a global epidemiological transition towards increased burden of non-communicable diseases, communicable diseases continue to cause substantial morbidity and mortality worldwide. Understanding the burden of a wide range of infectious diseases, and its variation by geography and age, is pivotal to research priority setting and resource mobilisation globally.

METHODS

We estimated disability-adjusted life-years (DALYs) associated with 85 pathogens in 2019, globally, regionally, and for 204 countries and territories. The term pathogen included causative agents, pathogen groups, infectious conditions, and aggregate categories. We applied a novel methodological approach to account for underlying, immediate, and intermediate causes of death, which counted every death for which a pathogen had a role in the pathway to death. We refer to this measure as the burden associated with infection, which was estimated by combining different sources of information. To compare the burden among all pathogens, we used pathogen-specific ratios to incorporate the burden of immediate and intermediate causes of death for pathogens modelled previously by the GBD. We created the ratios by using multiple cause of death data, hospital discharge data, linkage data, and minimally invasive tissue sampling data to estimate the fraction of deaths coming from the pathway to death chain. We multiplied the pathogen-specific ratios by age-specific years of life lost (YLLs), calculated with GBD 2019 methods, and then added the adjusted YLLs to age-specific years lived with disability (YLDs) from GBD 2019 to produce adjusted DALYs to account for deaths in the chain. We used standard GBD methods to calculate 95% uncertainty intervals (UIs) for final estimates of DALYs by taking the 2·5th and 97·5th percentiles across 1000 posterior draws for each quantity of interest. We provided burden estimates pertaining to all ages and specifically to the under 5 years age group.

FINDINGS

Globally in 2019, an estimated 704 million (95% UI 610-820) DALYs were associated with 85 different pathogens, including 309 million (250-377; 43·9% of the burden) in children younger than 5 years. This burden accounted for 27·7% (and 65·5% in those younger than 5 years) of the previously reported total DALYs from all causes in 2019. Comparing super-regions, considerable differences were observed in the estimated pathogen-associated burdens in relation to DALYs from all causes, with the highest burden observed in sub-Saharan Africa (314 million [270-368] DALYs; 61·5% of total regional burden) and the lowest in the high-income super-region (31·8 million [25·4-40·1] DALYs; 9·8%). Three leading pathogens were responsible for more than 50 million DALYs each in 2019: tuberculosis (65·1 million [59·0-71·2]), malaria (53·6 million [27·0-91·3]), and HIV or AIDS (52·1 million [46·6-60·9]). Malaria was the leading pathogen for DALYs in children younger than 5 years (37·2 million [17·8-64·2]). We also observed substantial burden associated with previously less recognised pathogens, including Staphylococcus aureus and specific Gram-negative bacterial species (ie, Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Acinetobacter baumannii, and Helicobacter pylori). Conversely, some pathogens had a burden that was smaller than anticipated.

INTERPRETATION

Our detailed breakdown of DALYs associated with a comprehensive list of pathogens on a global, regional, and country level has revealed the magnitude of the problem and helps to indicate where research funding mismatch might exist. Given the disproportionate impact of infection on low-income and middle-income countries, an essential next step is for countries and relevant stakeholders to address these gaps by making targeted investments.

FUNDING

Bill & Melinda Gates Foundation, Wellcome Trust, and Department of Health and Social Care using UK aid funding managed by the Fleming Fund.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/eaf2ad5a918b/gr4a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/7efb9e1c145a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/001bacb68c57/gr2a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/c41e49065215/gr3a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/eaf2ad5a918b/gr4a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/7efb9e1c145a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/001bacb68c57/gr2a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/c41e49065215/gr3a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ea/11269650/eaf2ad5a918b/gr4a.jpg
摘要

背景

尽管全球传染病负担呈增加趋势,但非传染性疾病仍是全球主要的发病和致死原因。了解广泛的传染病负担及其在地理和年龄上的差异,对于全球的研究重点设定和资源调动至关重要。

方法

我们估算了 2019 年全球、各区域和 204 个国家和地区共 85 种病原体导致的残疾调整生命年(DALYs)。病原体一词包括病原体、病原体组、传染性疾病和综合类别。我们应用了一种新的方法来解释根本、直接和间接死因,这种方法将每种病原体导致的死亡都计入了死亡途径。我们将这种衡量方法称为感染相关负担,通过结合不同来源的信息来估计。为了比较所有病原体的负担,我们使用了病原体特异性比值,纳入了之前由全球疾病负担研究(GBD)模型化的直接和间接死因的负担。我们通过使用多死因数据、住院数据、关联数据和微创组织采样数据来创建这些比值,以估计死亡途径中来自病原体的死亡比例。我们将病原体特异性比值乘以 GBD 2019 方法计算的特定年龄的生命损失年(YLLs),然后将调整后的 YLLs添加到 GBD 2019 的特定年龄的残疾生活年(YLDs)中,以产生考虑到链中死亡的调整后的 DALYs。我们使用标准的 GBD 方法,通过对每个感兴趣的数量进行 1000 次后验抽样的第 2.5 和第 97.5 个百分位数,计算 95%不确定性区间(UI)的最终估计值。我们提供了与所有年龄相关的负担估计值,特别是与 5 岁以下年龄组相关的负担估计值。

结果

2019 年,全球估计有 7.04 亿(95% UI 6.10-8.20)DALYs 与 85 种不同的病原体相关,其中 5 岁以下儿童有 3.09 亿(占负担的 43.9%)。这一负担占 2019 年所有病因总 DALYs 的 27.7%(5 岁以下儿童占 65.5%)。与所有病因的总 DALYs 相比,在超级区域之间,病原体相关的负担存在显著差异,其中撒哈拉以南非洲地区的负担最高(3.14 亿[270-368]DALYs;占总区域负担的 61.5%),高收入超级区域的负担最低(3180 万[25.4-40.1]DALYs;占 9.8%)。2019 年有三种主要病原体导致的 DALYs 超过 5000 万:结核病(6510 万[59.0-71.2])、疟疾(5360 万[27.0-91.3])和艾滋病毒/艾滋病(5210 万[46.6-60.9])。疟疾是 5 岁以下儿童的主要病原体(3720 万[17.8-64.2])。我们还发现了与以前较少被认识的病原体相关的大量负担,包括金黄色葡萄球菌和特定的革兰氏阴性细菌(即肺炎克雷伯菌、大肠杆菌、铜绿假单胞菌、鲍曼不动杆菌和幽门螺杆菌)。相反,一些病原体的负担比预期的要小。

解释

我们对全球、区域和国家层面的广泛病原体清单进行了详细的 DALYs 细分,揭示了问题的严重程度,并有助于表明研究资金的错配可能存在的地方。鉴于感染对低收入和中等收入国家的不成比例的影响,下一步的关键是国家和相关利益攸关方通过有针对性的投资来解决这些差距。

资助

比尔和梅琳达·盖茨基金会、惠康信托基金会和英国卫生部,利用英国援助资金,由弗莱明基金管理。

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