代谢功能障碍和酒精相关性肝病:综述

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Nicholas Dunn, Naim Al-Khouri, Ismail Abdellatif, Ashwani K Singal
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引用次数: 0

摘要

摘要:脂肪变性肝病这个术语现在被用来描述肝脏中脂肪堆积的情况。脂肪变性肝病一词包括一系列明确的和不太明确的疾病;代谢功能障碍相关脂肪变性肝病(MASLD),酒精相关肝病(ALD),以及代谢和酒精相关肝病(Met-ALD),其中心脏代谢危险因素,如肥胖,糖尿病或血脂异常,和酒精消耗在疾病的发生和进展中起作用。Met-ALD被定义为男性肝病,至少有一种心脏代谢危险因素,每周饮酒210-420克(每天约30-60克),而对于女性,它被定义为除了每周饮酒140-350克(每天约20-50克)之外,至少有一种心脏代谢危险因素。这一酒精摄入量水平超过了传统上用于排除酒精作为MASLD的一个促成因素的阈值,但仍低于典型ALD的典型相关水平。据估计,Met-ALD影响了美国约1700万人。它是一种独特的疾病,有肝硬化、肝细胞癌和死亡率的风险,不同于MASLD或ALD。其治疗主要依靠减肥、戒酒和控制心脏代谢危险因素。新型药物如胰高血糖素样肽-1激动剂和成纤维细胞生长因子-21类似物可能是治疗MetALD的有希望的未来治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic Dysfunction and Alcohol-Associated Liver Disease: A Narrative Review.

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.

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来源期刊
Clinical and Translational Gastroenterology
Clinical and Translational Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.00
自引率
0.00%
发文量
114
审稿时长
16 weeks
期刊介绍: Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease. Colon and small bowel Endoscopy and novel diagnostics Esophagus Functional GI disorders Immunology of the GI tract Microbiology of the GI tract Inflammatory bowel disease Pancreas and biliary tract Liver Pathology Pediatrics Preventative medicine Nutrition/obesity Stomach.
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