Suppr超能文献

代谢功能障碍与酒精性肝病:一篇叙述性综述

Metabolic Dysfunction and Alcohol-Associated Liver Disease: A Narrative Review.

作者信息

Dunn Nicholas, Al-Khouri Naim, Abdellatif Ismail, Singal Ashwani K

机构信息

Department of Medicine, Kansas University Medical Center, Kansas City, Kansas, USA.

Department of Hepatology, Arizona Liver Health, Phoenix, Arizona, USA.

出版信息

Clin Transl Gastroenterol. 2025 May 1;16(5):e00828. doi: 10.14309/ctg.0000000000000828.

Abstract

The term steatotic liver disease (SLD) is now used to describe conditions involving fat accumulation in the liver. SLD term includes a spectrum of defined and less defined disorders: metabolic dysfunction-associated SLD (MASLD), alcohol-associated liver disease (ALD), and metabolic and ALD (Met-ALD), where both cardiometabolic risk factors, such as obesity, diabetes, or dyslipidemia, and alcohol consumption function in disease development and progression. Met-ALD is defined as liver disease in men with at least 1 cardiometabolic risk factor who also consume 210-420 g of alcohol per week (approximately 30-60 g per day), whereas for women, it is defined as at least 1 cardiometabolic risk factor in addition to consumption of 140-350 g of alcohol per week (approximately 20-50 g per day). This level of alcohol intake exceeds the thresholds traditionally used to exclude alcohol as a contributing factor in MASLD, but it remains below the levels typically associated with classic ALD. Met-ALD is estimated to affect about 17 million people in the United States It is a unique disease with the risk of cirrhosis, hepatocellular carcinoma, and mortality different from those with MASLD or ALD. Its treatment relies mainly on weight loss, alcohol abstinence, and control of cardiometabolic risk factors. Novel medications such as glucagon-like peptide-1 agonists and fibroblast growth factor s21 analogs may be promising future therapies for the treatment of Met-ALD.

摘要

脂肪性肝病(SLD)这一术语现用于描述涉及肝脏脂肪堆积的病症。SLD术语包括一系列明确和不太明确的疾病:代谢功能障碍相关的SLD(MASLD)、酒精性肝病(ALD)以及代谢性和酒精性肝病(Met-ALD),其中肥胖、糖尿病或血脂异常等心脏代谢危险因素以及饮酒在疾病的发生和发展中都起作用。Met-ALD被定义为患有至少一种心脏代谢危险因素且每周饮酒210 - 420克(约每天30 - 60克)的男性的肝病,而对于女性,其定义为除每周饮酒140 - 350克(约每天20 - 50克)外还患有至少一种心脏代谢危险因素。这种酒精摄入量超过了传统上用于排除酒精作为MASLD促成因素的阈值,但仍低于通常与典型ALD相关的水平。据估计,在美国Met-ALD影响约1700万人。它是一种独特的疾病,其肝硬化、肝细胞癌风险和死亡率与MASLD或ALD不同。其治疗主要依赖于体重减轻、戒酒以及控制心脏代谢危险因素。胰高血糖素样肽-1激动剂和成纤维细胞生长因子s21类似物等新型药物可能是未来治疗Met-ALD的有前景的疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0994/12101925/49183a7adb2f/ct9-16-e00828-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验