Lancet Gastroenterol Hepatol. 2020 Mar;5(3):245-266. doi: 10.1016/S2468-1253(19)30349-8. Epub 2020 Jan 22.
Cirrhosis and other chronic liver diseases (collectively referred to as cirrhosis in this paper) are a major cause of morbidity and mortality globally, although the burden and underlying causes differ across locations and demographic groups. We report on results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 on the burden of cirrhosis and its trends since 1990, by cause, sex, and age, for 195 countries and territories.
We used data from vital registrations, vital registration samples, and verbal autopsies to estimate mortality. We modelled prevalence of total, compensated, and decompensated cirrhosis on the basis of hospital and claims data. Disability-adjusted life-years (DALYs) were calculated as the sum of years of life lost due to premature death and years lived with disability. Estimates are presented as numbers and age-standardised or age-specific rates per 100 000 population, with 95% uncertainty intervals (UIs). All estimates are presented for five causes of cirrhosis: hepatitis B, hepatitis C, alcohol-related liver disease, non-alcoholic steatohepatitis (NASH), and other causes. We compared mortality, prevalence, and DALY estimates with those expected according to the Socio-demographic Index (SDI) as a proxy for the development status of regions and countries.
In 2017, cirrhosis caused more than 1·32 million (95% UI 1·27-1·45) deaths (440 000 [416 000-518 000; 33·3%] in females and 883 000 [838 000-967 000; 66·7%] in males) globally, compared with less than 899 000 (829 000-948 000) deaths in 1990. Deaths due to cirrhosis constituted 2·4% (2·3-2·6) of total deaths globally in 2017 compared with 1·9% (1·8-2·0) in 1990. Despite an increase in the number of deaths, the age-standardised death rate decreased from 21·0 (19·2-22·3) per 100 000 population in 1990 to 16·5 (15·8-18·1) per 100 000 population in 2017. Sub-Saharan Africa had the highest age-standardised death rate among GBD super-regions for all years of the study period (32·2 [25·8-38·6] deaths per 100 000 population in 2017), and the high-income super-region had the lowest (10·1 [9·8-10·5] deaths per 100 000 population in 2017). The age-standardised death rate decreased or remained constant from 1990 to 2017 in all GBD regions except eastern Europe and central Asia, where the age-standardised death rate increased, primarily due to increases in alcohol-related liver disease prevalence. At the national level, the age-standardised death rate of cirrhosis was lowest in Singapore in 2017 (3·7 [3·3-4·0] per 100 000 in 2017) and highest in Egypt in all years since 1990 (103·3 [64·4-133·4] per 100 000 in 2017). There were 10·6 million (10·3-10·9) prevalent cases of decompensated cirrhosis and 112 million (107-119) prevalent cases of compensated cirrhosis globally in 2017. There was a significant increase in age-standardised prevalence rate of decompensated cirrhosis between 1990 and 2017. Cirrhosis caused by NASH had a steady age-standardised death rate throughout the study period, whereas the other four causes showed declines in age-standardised death rate. The age-standardised prevalence of compensated and decompensated cirrhosis due to NASH increased more than for any other cause of cirrhosis (by 33·2% for compensated cirrhosis and 54·8% for decompensated cirrhosis) over the study period. From 1990 to 2017, the number of prevalent cases more than doubled for compensated cirrhosis due to NASH and more than tripled for decompensated cirrhosis due to NASH. In 2017, age-standardised death and DALY rates were lower among countries and territories with higher SDI.
Cirrhosis imposes a substantial health burden on many countries and this burden has increased at the global level since 1990, partly due to population growth and ageing. Although the age-standardised death and DALY rates of cirrhosis decreased from 1990 to 2017, numbers of deaths and DALYs and the proportion of all global deaths due to cirrhosis increased. Despite the availability of effective interventions for the prevention and treatment of hepatitis B and C, they were still the main causes of cirrhosis burden worldwide, particularly in low-income countries. The impact of hepatitis B and C is expected to be attenuated and overtaken by that of NASH in the near future. Cost-effective interventions are required to continue the prevention and treatment of viral hepatitis, and to achieve early diagnosis and prevention of cirrhosis due to alcohol-related liver disease and NASH.
Bill & Melinda Gates Foundation.
肝硬化和其他慢性肝病(在本文中统称为肝硬化)是全球发病率和死亡率的主要原因,尽管在不同地点和人口群体中,负担和根本原因存在差异。我们报告了 2017 年全球疾病、伤害和危险因素研究(GBD)关于自 1990 年以来肝硬化的负担及其趋势的结果,按病因、性别和年龄进行了分类,涵盖了 195 个国家和地区。
我们使用来自生命登记、生命登记样本和死因推断的数据来估计死亡率。我们根据医院和索赔数据,对总肝硬化、代偿性肝硬化和失代偿性肝硬化的流行率进行建模。利用失能调整生命年(DALY)来衡量由于过早死亡而导致的生命损失年数和由于残疾而导致的生命损失年数。我们报告的估计数是每 10 万人中患有肝硬化的人数以及年龄标准化或年龄特异性发病率,置信区间为 95%。所有估计数均基于乙型肝炎、丙型肝炎、酒精性肝病、非酒精性脂肪性肝炎(NASH)和其他原因引起的五种肝硬化原因。我们将死亡率、流行率和 DALY 估计值与社会人口指数(SDI)预期的死亡率、流行率和 DALY 进行了比较,SDI 是衡量区域和国家发展状况的替代指标。
2017 年,肝硬化导致全球超过 132 万人(95%UI 127-145;440 万[416-518;33.3%]为女性,883 万[838-967;66.7%]为男性)死亡,而 1990 年的死亡人数不到 899 万(829-948)。2017 年,肝硬化导致的死亡占全球总死亡人数的 2.4%(2.3-2.6),而 1990 年为 1.9%(1.8-2.0)。尽管死亡人数有所增加,但年龄标准化死亡率从 1990 年的每 10 万人 21.0(19.2-22.3)下降到 2017 年的每 100 000 人 16.5(15.8-18.1)。在整个研究期间,所有年份中,撒哈拉以南非洲在 GBD 超地区的年龄标准化死亡率最高(2017 年为每 10 万人 32.2[25.8-38.6]死亡),而高收入超地区的年龄标准化死亡率最低(2017 年为每 10 万人 10.1[9.8-10.5]死亡)。除了东欧和中亚之外,所有 GBD 地区的年龄标准化死亡率在 1990 年至 2017 年期间均有所下降或保持不变,东欧和中亚的年龄标准化死亡率上升,主要是由于酒精性肝病的流行率上升。在国家层面,2017 年新加坡的肝硬化年龄标准化死亡率最低(每 10 万人 3.7[3.3-4.0]),而自 1990 年以来,埃及每年的肝硬化年龄标准化死亡率均为最高(2017 年为每 10 万人 103.3[64.4-133.4])。2017 年全球有 1060 万(103-109)例失代偿性肝硬化和 1.12 亿(1.07-1.19)例代偿性肝硬化。1990 年至 2017 年,失代偿性肝硬化的年龄标准化流行率显著上升。在整个研究期间,NASH 引起的肝硬化死亡率保持稳定,而其他四种原因的肝硬化死亡率呈下降趋势。在整个研究期间,NASH 引起的代偿性和失代偿性肝硬化的年龄标准化流行率增长幅度最大(代偿性肝硬化增长 33.2%,失代偿性肝硬化增长 54.8%)。1990 年至 2017 年,NASH 引起的代偿性肝硬化的病例数增加了一倍以上,NASH 引起的失代偿性肝硬化的病例数增加了两倍以上。2017 年,SDI 较高的国家和地区的肝硬化死亡和 DALY 率较低。
肝硬化给许多国家带来了沉重的健康负担,自 1990 年以来,全球的负担有所增加,这在一定程度上是由于人口增长和老龄化。尽管 1990 年至 2017 年期间肝硬化的年龄标准化死亡率和 DALY 率有所下降,但死亡人数和 DALY 以及全球死亡人数中肝硬化的比例有所增加。尽管有有效的预防和治疗乙型肝炎和丙型肝炎的干预措施,但它们仍是全球肝硬化负担的主要原因,尤其是在低收入国家。预计乙型肝炎和丙型肝炎的影响将减弱,并被 NASH 的影响所取代。需要采取具有成本效益的干预措施,继续预防和治疗病毒性肝炎,并实现对酒精性肝病和 NASH 引起的肝硬化的早期诊断和预防。
比尔及梅琳达·盖茨基金会。