Metabolic associated steatotic liver disease misses fewer high-risk patients than metabolic associated fatty liver disease.

IF 1.5 Q3 GASTROENTEROLOGY & HEPATOLOGY
Clinical and Experimental Hepatology Pub Date : 2024-12-01 Epub Date: 2024-12-02 DOI:10.5114/ceh.2024.145429
Yu-Ming Cheng, Tsung-Han Hsieh, Shan-Wen Wang, Chia-Chi Wang, Jia-Horng Kao
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引用次数: 0

Abstract

Aim of the study: Metabolic associated steatotic liver disease (MASLD) was proposed to replace non-alcoholic fatty liver disease (NAFLD) in 2023. It has different diagnostic criteria from metabolic associated fatty liver disease (MAFLD). The comparison between the two disease names and diagnostic criteria deserves investigation.

Material and methods: We recruited participants from the Taiwan Bio-bank database. NAFLD was diagnosed based on the presence of hepatic steatosis after excluding chronic hepatitis B or C virus infection, chronic drinkers, or other known liver diseases. According to the presence of cardiometabolic criteria, NAFLD is divided into two groups: MASLD and cryptogenic steatotic liver disease (SLD). The "missing" group was defined as those patients who met the diagnostic criteria for MASLD but not for MAFLD. Cryptogenic SLD was used as the control group. We used the NAFLD fibrosis score (NFS) as an indicator for liver fibrosis.

Results: This study included 17,595 participants, among whom 7,274 (41.3%) had MASLD, and 6,905 had pure MAFLD, defined as MAFLD having no other causes of liver diseases. The cryptogenic SLD group consisted of 264 (1.5%) patients, while the "missing" group had 369 patients. There were no differences in metabolic parameters, liver markers and the percentage of carotid plaques between these two groups. When comparing the "missing" group to the control group, the "missing" group had higher NFS and a higher proportion of carotid plaques.

Conclusions: In this large, population-based study, is not advisable to exclude the "missing" group having higher risk of liver fibrosis and atherosclerosis than controls. MASLD misses fewer high-risk patients than pure MAFLD for replacing NAFLD.

代谢性脂肪变性肝病比代谢性脂肪性肝病漏掉的高危患者更少。
研究目的:代谢相关脂肪变性肝病(MASLD)被提议在2023年取代非酒精性脂肪性肝病(NAFLD)。它与代谢性相关脂肪肝(MAFLD)有不同的诊断标准。两种疾病名称和诊断标准的比较值得研究。材料与方法:我们从台湾生物库数据库中招募受试者。在排除慢性乙型或丙型肝炎病毒感染、慢性饮酒者或其他已知肝脏疾病后,根据肝脂肪变性的存在诊断NAFLD。根据存在的心脏代谢标准,NAFLD分为两组:MASLD和隐源性脂肪变性肝病(SLD)。“缺失”组定义为符合MASLD诊断标准但不符合MAFLD诊断标准的患者。以隐源性SLD为对照组。我们使用NAFLD纤维化评分(NFS)作为肝纤维化的指标。结果:该研究包括17,595名参与者,其中7,274名(41.3%)患有MASLD, 6,905名患有纯粹的MAFLD,定义为没有其他肝脏疾病原因的MAFLD。隐源性SLD组有264例(1.5%),而“缺失”组有369例。两组之间的代谢参数、肝脏标志物和颈动脉斑块百分比没有差异。当将“缺失”组与对照组比较时,“缺失”组有更高的NFS和更高的颈动脉斑块比例。结论:在这项以人群为基础的大型研究中,不建议排除肝纤维化和动脉粥样硬化风险高于对照组的“缺失”组。在替代NAFLD时,MASLD比单纯MAFLD漏掉的高危患者更少。
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来源期刊
Clinical and Experimental Hepatology
Clinical and Experimental Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
2.80
自引率
0.00%
发文量
32
期刊介绍: Clinical and Experimental Hepatology – quarterly of the Polish Association for Study of Liver – is a scientific and educational, peer-reviewed journal publishing original and review papers describing clinical and basic investigations in the field of hepatology.
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