Metabolic characteristics of patients with MetALD: Caveats of a new definition

胰岛素抵抗 天冬氨酸转氨酶 医学 丙氨酸转氨酶 脂肪变性 内科学 代谢综合征 转氨酶 脂肪肝 体质指数 胃肠病学 血压 糖尿病 瞬态弹性成像 酒精性肝病 内分泌学 肝病 肝硬化 胰岛素 肥胖 疾病 生物 肝纤维化 生物化学 碱性磷酸酶
作者
Erin Petrie,Meagan Gray,Fernando Bril
出处
期刊:Liver International [Wiley]
卷期号:44 (11): 2929-2938 被引量:15
标识
DOI:10.1111/liv.16034
摘要

Abstract Background and Aims Recently, a new entity was introduced, MetALD, which includes patients with metabolic dysfunction‐associated steatotic liver disease (MASLD), who consume moderate amounts of alcohol. However, little is known regarding the metabolic and clinical characteristics of these patients. Methods Data from the National Health and Nutrition Examination Surveys 2017–2020 was used. Participants without valid transient elastography (TE) measurements, incomplete alcohol consumption report, or with alternative etiologies of liver steatosis were excluded. Results A total of 6901 patients were included in the study, of which 106 (1.5%) had MetALD. Overall, MetALD patients showed a metabolic profile that was more similar to patients with alcohol related liver disease (ALD) than MASLD. Specifically, while patients with MetALD showed values in‐between MASLD and ALD for body mass index (BMI), aspartate transaminase (AST), alanine transaminase (ALT), gamma glutamyltransferase (GGT) and haemoglobin A1c, they had similar high‐density lipoprotein cholesterol (HDL‐C), blood pressure, prevalence of diabetes and insulin resistance to ALD patients. Increasing alcohol consumption was associated with lower insulin resistance and A1c and higher triglycerides, HDL‐C and blood pressure. Moreover, while AST, ALT and GGT increased with alcohol consumption, this did not translate into worse hepatic steatosis or liver fibrosis by TE. Conclusions MetALD patients share some characteristics with MASLD, but they resemble ALD patients more, especially after adjusting for BMI. Alcohol consumption produces a dissociation between insulin resistance and some cardiometabolic risk factors (blood pressure and HDL‐C), which may make the current classification of patients challenging.
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