Current burden of steatotic liver disease and fibrosis among adults in the United States, 2017-2023.

IF 16.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Clinical and Molecular Hepatology Pub Date : 2025-04-01 Epub Date: 2024-11-29 DOI:10.3350/cmh.2024.0987
Donghee Kim, Pojsakorn Danpanichkul, Karn Wijarnpreecha, George Cholankeril, Rohit Loomba, Aijaz Ahmed
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Abstract

Background/aims: Multi-society experts proposed the adoption of new terminology, metabolic dysfunctionassociated steatotic liver disease (MASLD) and steatotic liver disease (SLD). We studied the current prevalence of SLD and its subcategories in the US.

Methods: Using the recent National Health and Nutrition Examination Survey from 2017 to 2023, we analyzed data from 12,199 participants (≥18 years) who completed transient elastography. SLD and its subcategories, including MASLD, metabolic and alcohol-related liver disease (MetALD), and alcohol-related liver disease (ALD), were categorized according to consensus nomenclature.

Results: The age-adjusted prevalence of SLD (cut-off: 285 dB/m) was 35.0% (95% confidence interval [CI] 33.4-36.7). Within this category, the age-adjusted prevalence for MASLD was 31.9% (95% CI 30.4-33.4), MetALD 2.2% (95% CI 1.8-2.6), and ALD 0.8% (95% CI 0.6-1.1). The prevalence of SLD and MASLD showed a statistically insignificant decrease during COVID-19, while ALD increased without significance. In contrast, the prevalence of advanced fibrosis in SLD was significantly higher during the COVID-19 era, at 9.8% for 285 dB/m and 7.8% for 263 dB/m, compared to 7.4% (P=0.039) and 6% (P=0.041) in the pre-COVID-19 era. The proportion of advanced fibrosis and cirrhosis in individuals with ALD was two-fold higher than MASLD and MetALD, largely due to increases during the COVID-19 era.

Conclusion: While the prevalence of SLD and its subcategories remained stable, there was a significant increase in advanced fibrosis among SLD individuals during the COVID-19 era, with ALD having a proportion of advanced fibrosis and cirrhosis that was twice as high as MASLD and MetALD.

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2017-2023年美国成年人脂肪变性肝病和纤维化的当前负担
背景/目的:多社会专家提出采用新的术语,代谢功能障碍相关脂肪变性肝病(MASLD)和脂肪变性肝病(SLD)。我们研究了美国目前的SLD患病率及其子类。方法:利用最近的2017年至2023年全国健康与营养检查调查,我们分析了完成瞬态弹性成像的12199名参与者(≥18岁)的数据。SLD及其亚类,包括MASLD、代谢性和酒精相关肝病(MetALD)和酒精相关肝病(ALD),根据一致的命名法进行分类。结果:经年龄调整的SLD患病率(截止值:285 dB/m)为35.0%(95%可信区间[CI]: 33.4-36.7)。在这一类别中,MASLD的年龄调整患病率为31.9% (95% CI: 30.4-33.4), MetALD为2.2% (95% CI: 1.8-2.6), ALD为0.8% (95% CI: 0.6-1.1)。在COVID-19期间,SLD和MASLD患病率下降无统计学意义,而ALD患病率升高无统计学意义。相比之下,在COVID-19时代,SLD晚期纤维化的患病率明显更高,285 dB/m为9.8%,263 dB/m为7.8%,而在COVID-19前时代为7.4% (P=0.039)和6% (P=0.041)。ALD患者的晚期纤维化和肝硬化比例是MASLD和MetALD的两倍,主要是由于在COVID-19时代增加。结论:虽然SLD及其亚类的患病率保持稳定,但在COVID-19时代,SLD患者的晚期纤维化显著增加,ALD患者的晚期纤维化和肝硬化比例是MASLD和MetALD的两倍。
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来源期刊
Clinical and Molecular Hepatology
Clinical and Molecular Hepatology Medicine-Hepatology
CiteScore
15.60
自引率
9.00%
发文量
89
审稿时长
10 weeks
期刊介绍: Clinical and Molecular Hepatology is an internationally recognized, peer-reviewed, open-access journal published quarterly in English. Its mission is to disseminate cutting-edge knowledge, trends, and insights into hepatobiliary diseases, fostering an inclusive academic platform for robust debate and discussion among clinical practitioners, translational researchers, and basic scientists. With a multidisciplinary approach, the journal strives to enhance public health, particularly in the resource-limited Asia-Pacific region, which faces significant challenges such as high prevalence of B viral infection and hepatocellular carcinoma. Furthermore, Clinical and Molecular Hepatology prioritizes epidemiological studies of hepatobiliary diseases across diverse regions including East Asia, North Asia, Southeast Asia, Central Asia, South Asia, Southwest Asia, Pacific, Africa, Central Europe, Eastern Europe, Central America, and South America. The journal publishes a wide range of content, including original research papers, meta-analyses, letters to the editor, case reports, reviews, guidelines, editorials, and liver images and pathology, encompassing all facets of hepatology.
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