Steatotic liver disease: non-invasive assessment and biomarkers across metabolic dysfunction-associated steatotic liver disease, metabolic dysfunction-associated steatotic liver disease with moderate alcohol consumption and alcohol-associated liver disease.

IF 21.7 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Clinical and Molecular Hepatology Pub Date : 2026-09-01 Epub Date: 2026-07-15 DOI:10.3350/cmh.2026.0415
Monica Tincopa, Rohit Loomba
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引用次数: 0

Abstract

Steatotic liver disease (SLD) is a leading cause of chronic liver disease worldwide impacting more than 30% of the adult population. With the rise of obesity, metabolic syndrome and alcohol use disorder, the prevalence of the two main subtypes of SLD - metabolic dysfunction-associated steatotic liver disease (MASLD) and alcohol-associated liver disease (ALD) - continues to increase. There has concurrently been an acknowledgement of a third subtype of SLD-metabolic dysfunction-associated steatotic liver disease with moderate alcohol consumption (MetALD)- wherein an individual has both components of metabolic dysfunction and regular alcohol intake. The public health significance of the SLD epidemic is substantial given risk for progression to cirrhosis, end-stage liver disease and development of hepatocellular carcinoma. Individuals with stage two fibrosis or above and those with active inflammation with hepatocyte injury are at highest risk for adverse liver-related outcomes and overall mortality. Current screening and risk stratification recommendations highlight the importance of identifying individuals at highest risk of clinical outcomes using non-invasive testing (NIT) as these individuals would benefit from liver-directed pharmacotherapy. Importantly, the performance of NITs can vary substantially based on NIT selected, cut points applied and patient population evaluated. The evidence base for NIT performance is strongest in MASLD with comparatively limited data in ALD and emerging data in MetALD. This review discusses NIT diagnostic performance in SLD and their role in chronic disease management.

脂肪变性肝病:MASLD、MetALD和ALD的无创评估和生物标志物。
脂肪变性肝病(SLD)是全球慢性肝病的主要原因,影响超过30%的成人人口。随着肥胖、代谢综合征和酒精使用障碍的增加,SLD的两种主要亚型——代谢功能障碍相关脂肪变性肝病(MASLD)和酒精相关肝病(ALD)——的患病率继续增加。同时也承认第三种SLD亚型- MetALD-其中个体既有代谢功能障碍的组成部分,又有规律的酒精摄入。考虑到发展为肝硬化、终末期肝病和肝细胞癌(HCC)的风险,SLD流行的公共卫生意义是重大的。2期或以上纤维化患者以及伴有肝细胞损伤的活动性炎症患者发生肝脏相关不良结局和总死亡率的风险最高。目前的筛查和风险分层建议强调了使用非侵入性检测(NIT)识别临床结果风险最高的个体的重要性,因为这些个体将受益于肝脏定向药物治疗。重要的是,NIT的性能可以根据NIT的选择、应用的切割点和评估的患者群体而有很大的不同。NIT性能的证据基础在MASLD中最强,在ALD中数据相对有限,在MetALD中数据新兴。本文综述了NIT在SLD诊断中的表现及其在慢性疾病治疗中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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