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非侵入性筛查、分期和代谢相关脂肪性肝病(MAFLD)在 2 型糖尿病患者中的管理:我们目前了解多少?

Non-invasive screening, staging and management of metabolic dysfunction-associated fatty liver disease (MAFLD) in type 2 diabetes mellitus patients: what do we know so far ?

机构信息

Service d'Hépato-Gastroentérologie, Cliniques universitaires Saint-Luc, UCLouvain, Brussels, Belgium.

Service d'Endocrinologie et Nutrition, Cliniques universitaires Saint-Luc, UCLouvain, Brussels, Belgium.

出版信息

Acta Gastroenterol Belg. 2022 Apr-Jun;85(2):346-357. doi: 10.51821/85.2.9775.

Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD) is the evidence of steatosis in the setting of a metabolic risk condition such as type 2 diabetes mellitus (T2DM). Indeed, T2DM and liver steatosis share common pathophysiological mechanisms, and one can lead to the other. MAFLD can progress from simple steatosis to non-alcoholic steatohepatitis (NASH), fibrosis and cirrhosis as well as hepatocellular carcinoma (HCC). Because of the lack / disparity of guidelines for MAFLD screening, which is asymptomatic in its early stages, it is not rare that diabetic patients are belatedly diagnosed with NASH cirrhosis or HCC. We therefore recommend systematic non-invasive tests (NITs) that calculate an estimate of the risk based on readily available anthropometric and biological parameters. These include the fatty liver index (FLI) for steatosis detection and at least one of the following for fibrosis: non-alcoholic fatty liver disease fibrosis score (NFS), fibrosis-4 index (FIB-4) or Hepamet fibrosis score (HFS). Indeed, NFS and FIB-4 are the best predictors of liver-related events, while FIB-4 and HFS correlate with overall mortality. Systematic literature review found only few retrospective or cross-sectional studies using NITs for systematic steatosis and fibrosis screening in T2DM patients, with a crucial need for prospective studies. This screening strategy will allow targeted patients to be referred for further liver investigation (e.g. ultrasound, elastometry) and care. Current treatment modalities of MAFLD in T2DM patients range from lifestyle and dietary interventions to specific glucose-lowering drugs that recently showed some benefits regarding MAFLD, such as pioglitazone, glucagon-like peptide-1 receptor agonists and sodium-glucose cotransporter-2 inhibitors. Other treatments are currently under investigation.

摘要

代谢相关脂肪性肝病(MAFLD)是在 2 型糖尿病(T2DM)等代谢风险情况下发生脂肪变性的证据。事实上,T2DM 和肝脂肪变性具有共同的病理生理机制,一种疾病可导致另一种疾病。MAFLD 可从单纯性脂肪变性进展为非酒精性脂肪性肝炎(NASH)、纤维化和肝硬化以及肝细胞癌(HCC)。由于缺乏/指南不一致,MAFLD 筛查无症状,早期阶段筛查不足,糖尿病患者被迟诊为 NASH 肝硬化或 HCC 并不罕见。因此,我们建议进行系统的无创检测(NIT),这些检测根据易于获得的人体测量和生物学参数计算风险估计。这些检测包括脂肪性肝病指数(FLI)用于检测脂肪变性,以及以下至少一种用于纤维化检测:非酒精性脂肪性肝病纤维化评分(NFS)、纤维化-4 指数(FIB-4)或 Hepamet 纤维化评分(HFS)。事实上,NFS 和 FIB-4 是预测肝脏相关事件的最佳指标,而 FIB-4 和 HFS 与总死亡率相关。系统文献回顾发现,只有少数使用 NIT 进行 T2DM 患者系统性脂肪变性和纤维化筛查的回顾性或横断面研究,迫切需要前瞻性研究。这种筛查策略将使有针对性的患者能够接受进一步的肝脏检查(如超声、弹性成像)和治疗。目前 T2DM 患者 MAFLD 的治疗方法包括生活方式和饮食干预,以及最近在 MAFLD 方面显示出一些益处的特定降糖药物,如吡格列酮、胰高血糖素样肽-1 受体激动剂和钠-葡萄糖共转运蛋白-2 抑制剂。其他治疗方法正在研究中。

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