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全球、区域和国家多发性硬化症负担 1990-2016 年:2016 年全球疾病负担研究的系统分析。

Global, regional, and national burden of multiple sclerosis 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.

出版信息

Lancet Neurol. 2019 Mar;18(3):269-285. doi: 10.1016/S1474-4422(18)30443-5. Epub 2019 Jan 21.

Abstract

BACKGROUND

Multiple sclerosis is the most common inflammatory neurological disease in young adults. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) provides a systematic method of quantifying various effects of a given condition by demographic variables and geography. In this systematic analysis, we quantified the global burden of multiple sclerosis and its relationship with country development level.

METHODS

We assessed the epidemiology of multiple sclerosis from 1990 to 2016. Epidemiological outcomes for multiple sclerosis were modelled with DisMod-MR version 2.1, a Bayesian meta-regression framework widely used in GBD epidemiological modelling. Assessment of multiple sclerosis as the cause of death was based on 13 110 site-years of vital registration data analysed in the GBD's cause of death ensemble modelling module, which is designed to choose the optimum combination of mathematical models and predictive covariates based on out-of-sample predictive validity testing. Data on prevalence and deaths are summarised in the indicator, disability-adjusted life-years (DALYs), which was calculated as the sum of years of life lost (YLLs) and years of life lived with a disability. We used the Socio-demographic Index, a composite indicator of income per person, years of education, and fertility, to assess relations with development level.

FINDINGS

In 2016, there were 2 221 188 prevalent cases of multiple sclerosis (95% uncertainty interval [UI] 2 033 866-2 436 858) globally, which corresponded to a 10·4% (9·1 to 11·8) increase in the age-standardised prevalence since 1990. The highest age-standardised multiple sclerosis prevalence estimates per 100 000 population were in high-income North America (164·6, 95% UI, 153·2 to 177·1), western Europe (127·0, 115·4 to 139·6), and Australasia (91·1, 81·5 to 101·7), and the lowest were in eastern sub-Saharan Africa (3·3, 2·9-3·8), central sub-Saharan African (2·8, 2·4 to 3·1), and Oceania (2·0, 1·71 to 2·29). There were 18 932 deaths due to multiple sclerosis (95% UI 16 577 to 21 033) and 1 151 478 DALYs (968 605 to 1 345 776) due to multiple sclerosis in 2016. Globally, age-standardised death rates decreased significantly (change -11·5%, 95% UI -35·4 to -4·7), whereas the change in age-standardised DALYs was not significant (-4·2%, -16·4 to 0·8). YLLs due to premature death were greatest in the sixth decade of life (22·05, 95% UI 19·08 to 25·34). Changes in age-standardised DALYs assessed with the Socio-demographic Index between 1990 and 2016 were variable.

INTERPRETATION

Multiple sclerosis is not common but is a potentially severe cause of neurological disability throughout adult life. Prevalence has increased substantially in many regions since 1990. These findings will be useful for resource allocation and planning in health services. Many regions worldwide have few or no epidemiological data on multiple sclerosis, and more studies are needed to make more accurate estimates.

FUNDING

Bill & Melinda Gates Foundation.

摘要

背景

多发性硬化症是年轻人中最常见的炎症性神经系统疾病。全球疾病、伤害和危险因素研究(GBD)提供了一种系统的方法,可以通过人口统计学变量和地理位置来量化给定疾病的各种影响。在这项系统分析中,我们量化了多发性硬化症的全球负担及其与国家发展水平的关系。

方法

我们评估了 1990 年至 2016 年期间多发性硬化症的流行病学情况。采用 DisMod-MR 版本 2.1 对多发性硬化症的流行病学结果进行建模,该模型是 GBD 流行病学建模中广泛使用的贝叶斯荟萃回归框架。将多发性硬化症作为死亡原因的评估是基于 GBD 死因综合模型模块中分析的 13110 个地点-年的生命登记数据,该模块旨在根据样本外预测有效性测试选择最佳的数学模型和预测协变量组合。流行率和死亡率的数据汇总在残疾调整生命年(DALY)指标中,该指标是通过将生命损失年(YLL)和残疾生存年相加计算得出的。我们使用社会人口指数(Socio-demographic Index),一个由人均收入、受教育年限和生育率组成的综合指标,来评估与发展水平的关系。

结果

2016 年,全球有 2221188 例多发性硬化症的现患病例(95%置信区间[UI]为 2033866-2436858),与 1990 年相比,年龄标准化患病率增加了 10.4%(9.1%至 11.8%)。每 10 万人中多发性硬化症的年龄标准化患病率最高的估计值见于高收入的北美(164.6,95%UI,153.2 至 177.1)、西欧(127.0,115.4 至 139.6)和澳大拉西亚(91.1,81.5 至 101.7),而在撒哈拉以南非洲东部(3.3,2.9 至 3.8)、撒哈拉以南非洲中部(2.8,2.4 至 3.1)和大洋洲(2.0,1.71 至 2.29)则最低。2016 年,多发性硬化症导致 18932 人死亡(95%UI,16577 至 21033),1151478 人因多发性硬化症导致残疾调整生命年(968605 至 1345776)。全球范围内,年龄标准化死亡率显著下降(变化-11.5%,95%UI,-35.4 至-4.7),而年龄标准化残疾调整生命年的变化则不显著(-4.2%,-16.4 至 0.8)。由于过早死亡导致的 YLL 最大的是生命的第六个十年(22.05,95%UI,19.08 至 25.34)。1990 年至 2016 年期间,用社会人口指数评估的年龄标准化残疾调整生命年的变化是可变的。

解释

多发性硬化症并不常见,但在整个成年期都是一种潜在的严重的神经功能障碍的原因。自 1990 年以来,许多地区的多发性硬化症患病率大幅上升。这些发现将有助于卫生服务部门的资源配置和规划。世界上许多地区都缺乏多发性硬化症的流行病学数据,需要更多的研究来做出更准确的估计。

资金

比尔及梅琳达·盖茨基金会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fe6/6372756/5dd76c2ab456/gr1.jpg

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