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量化2000-2023年与儿童生长发育迟缓相关的疾病致死和非致死负担:全球疾病负担研究2023的系统分析

Quantifying the fatal and non-fatal burden of disease associated with child growth failure, 2000-2023: a systematic analysis from the Global Burden of Disease Study 2023.

出版信息

Lancet Child Adolesc Health. 2026 Jan;10(1):22-38. doi: 10.1016/S2352-4642(25)00303-7.

Abstract

BACKGROUND

Child growth failure (CGF), which includes underweight, wasting, and stunting, is among the factors most strongly associated with mortality and morbidity in children younger than 5 years worldwide. Poor height and bodyweight gain arise from a variety of biological and sociodemographic factors and are associated with increased vulnerability to infectious diseases. We used data from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2023 to estimate CGF prevalence, the risk of infectious diseases associated with CGF, and the disease mortality, morbidity, and overall burden associated with CGF.

METHODS

In this analysis we estimated the all-cause and cause-specific (diarrhoea, lower respiratory tract infections, malaria, and measles) disability-adjusted life-years (DALYs) lost and mortality associated with stunting, wasting, underweight, and CGF in aggregate. We combined the burden associated with mild, moderate, and severe forms of CGF: stunting was defined as height-for-age Z scores (HAZ) less than -1, underweight was defined as weight-for-age Z scores (WAZ) less than -1, and wasting was defined as weight-for-height Z scores (WHZ) less than -1, according to WHO Child Growth Standards. Population-level continuous distributions of HAZ, WAZ, and WHZ were estimated for 2000 to 2023 using data from surveys, literature, and individual-level study data. The risk of incidence of, and mortality due to, diarrhoea, lower respiratory infections, malaria, and measles was separately estimated in a meta-regression framework from longitudinal cohort data for Z scores less than -1. Finally, fatal outcomes associated with these diseases were estimated with vital registration, verbal autopsy, and case-fatality data, while non-fatal outcomes were estimated with surveys as well as health-care utilisation and case reporting data. The exposure prevalence and relative risk estimates were from continuous distributions, allowing for direct assessment of the attributable fractions for mild, moderate, and severe stunting, underweight, wasting, and the combined impact of child growth failure within populations. All estimates were age-specific, sex-specific, geography-specific, and year-specific.

FINDINGS

We estimated that, in children younger than 5 years in 2023, CGF was associated with 79·4 million (95% uncertainty interval [UI] 47·0-106) DALYs lost and 880 000 (517 000-1 170 000) deaths. This represented 17·9% (10·6-23·8) of 444 million (434-457) total under-5 DALYs and 18·8% (11·1-25·0) of all 4·67 million (4·59-4·75) under-5 deaths. Compared to stunting (33·0 million [24·1-42·2] DALYs, 373 000 [272 000-477 000] deaths) and wasting (39·2 million [23·8-53·0] DALYs, 428 000 [256 000-583 000] deaths), childhood underweight was associated with the largest share of CGF-related disease burden: 52·2 million (21·9-75·1) DALYs and 573 000 (236 000-824 000) deaths in children younger than 5 years in 2023.

INTERPRETATION

CGF remains a leading factor associated with death and disability in children younger than 5 years, despite global attention and focused interventions to reduce the prevalence of associated CGF indicators. Our findings underscore the need for policies, strategies, and interventions that focus on all indicators of CGF to reduce its associated health burden.

FUNDING

Gates Foundation.

摘要

背景

儿童生长发育不良(CGF),包括体重不足、消瘦和发育迟缓,是全球5岁以下儿童死亡率和发病率最密切相关的因素之一。身高和体重增长不佳源于多种生物学和社会人口学因素,并与传染病易感性增加有关。我们使用了《2023年全球疾病、伤害及风险因素负担研究》(GBD 2023)的数据来估计CGF患病率、与CGF相关的传染病风险以及与CGF相关的疾病死亡率、发病率和总体负担。

方法

在本分析中,我们估计了发育迟缓、消瘦、体重不足和总体CGF所导致的全因和特定病因(腹泻、下呼吸道感染、疟疾和麻疹)伤残调整生命年(DALYs)损失及死亡率。我们综合了轻度、中度和重度CGF形式的负担:根据世界卫生组织儿童生长标准,发育迟缓定义为年龄别身高Z评分(HAZ)低于-1,体重不足定义为年龄别体重Z评分(WAZ)低于-1,消瘦定义为身高别体重Z评分(WHZ)低于-1。利用调查、文献和个体水平研究数据估计了2000年至2023年HAZ、WAZ和WHZ的人群水平连续分布。在一个元回归框架中,根据Z评分低于-1的纵向队列数据,分别估计腹泻、下呼吸道感染、疟疾和麻疹的发病风险及死亡风险。最后,利用生命登记、口头尸检和病死率数据估计与这些疾病相关的致命结局,而非致命结局则通过调查以及医疗保健利用和病例报告数据进行估计。暴露患病率和相对风险估计来自连续分布,从而能够直接评估人群中轻度、中度和重度发育迟缓、体重不足、消瘦以及儿童生长发育不良综合影响的归因分数。所有估计均按年龄、性别、地理位置和年份进行了区分。

结果

我们估计,2023年5岁以下儿童中,CGF与7940万(95%不确定区间[UI] 4700 - 10600万)DALYs损失和88万(51.7万 - 117万)例死亡相关。这分别占5岁以下儿童4.44亿(4.34 - 4.57亿)总DALYs的17.9%(10.6% - 23.8%)和467万(459万 - 475万)所有5岁以下儿童死亡的18.8%(11.1% - 25.0%)。与发育迟缓(3300万[2410 - 4220万] DALYs,37.3万[27.2万 - 47.7万]例死亡)和消瘦(3920万[2380 - 5300万] DALYs,42.8万[25.6万 - 58.3万]例死亡)相比,儿童期体重不足与CGF相关疾病负担的占比最大:2023年5岁以下儿童中为5220万(2190 - 7510万)DALYs和57.3万(23.6万 - 82.4万)例死亡)。

解读

尽管全球对降低相关CGF指标患病率给予了关注并采取了针对性干预措施,但CGF仍然是5岁以下儿童死亡和残疾的主要相关因素。我们的研究结果强调需要制定侧重于CGF所有指标的政策、战略和干预措施,以减轻其相关的健康负担。

资金来源

盖茨基金会

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff78/12674951/ee5cea351fe0/gr1.jpg

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