Metabolic Dysfunction-associated Steatotic Liver Disease and Chronic Kidney Disease: From Epidemiology and Pathophysiology to Clinical Prediction and Treatment Options.

IF 6 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Jiacheng Liu, Cuiling Ma, Yafan Wang, Huiying Rao
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Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) and chronic kidney disease (CKD) have shown a significant increase in comorbidity on a global scale due to the prevalence of metabolic syndrome. In 2023, a number of academic societies formally proposed the concept of MASLD, superseding the previous terminology of "non-alcoholic fatty liver disease" and "metabolic dysfunction-associated fatty liver disease". The diagnostic criteria have been revised to place greater emphasis on the association between hepatic steatosis and cardiometabolic risk factors. MASLD constitutes an independent risk factor for CKD, with this risk potentially increasing in line with the severity of fatty degeneration and the progression of hepatic fibrosis. CKD may represent a potential risk factor for the progression of fibrosis in patients with MASLD. The interaction between the two conditions may accelerate the occurrence of cardiovascular events and increase the risk of all-cause mortality. MASLD and CKD may share core pathophysiological mechanisms, including genetic variants, insulin resistance, lipid metabolism disorders, chronic inflammation, oxidative stress, and gut microbiota dysbiosis. However, the bidirectional causal relationship between the two conditions and the molecular dialogue between organs remains unclear. Furthermore, there are significant gaps in clinical prediction tools and targeted treatment strategies for comorbidities. This paper reviews common pathophysiological mechanisms in MASLD and CKD, the epidemiological and clinical evidence linking MASLD to the risk of CKD, biomarkers and clinical prediction models for coexisting conditions, and potential therapeutic strategies. Our aim is to provide a theoretical basis for early identification, mechanism exploration, and clinical treatment of comorbidities.

代谢功能障碍相关的脂肪变性肝病和慢性肾病:从流行病学和病理生理学到临床预测和治疗选择。
由于代谢综合征的流行,代谢功能障碍相关的脂肪变性肝病(MASLD)和慢性肾脏疾病(CKD)在全球范围内的合并症显着增加。2023年,多个学会正式提出了MASLD的概念,取代了之前的“非酒精性脂肪性肝病”和“代谢功能障碍相关脂肪性肝病”的术语。诊断标准已经修订,以更加强调肝脂肪变性和心脏代谢危险因素之间的关系。MASLD是CKD的独立危险因素,随着脂肪变性的严重程度和肝纤维化的进展,这种风险可能会增加。CKD可能是MASLD患者纤维化进展的潜在危险因素。这两种情况之间的相互作用可能加速心血管事件的发生,并增加全因死亡的风险。MASLD和CKD可能有共同的核心病理生理机制,包括遗传变异、胰岛素抵抗、脂质代谢紊乱、慢性炎症、氧化应激和肠道微生物群失调。然而,这两种情况之间的双向因果关系和器官之间的分子对话仍不清楚。此外,在合并症的临床预测工具和靶向治疗策略方面存在显著差距。本文综述了MASLD和CKD的常见病理生理机制,MASLD与CKD风险之间的流行病学和临床证据,共存疾病的生物标志物和临床预测模型,以及潜在的治疗策略。我们的目的是为合并症的早期识别、机制探索和临床治疗提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical and Translational Hepatology
Journal of Clinical and Translational Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.40
自引率
2.80%
发文量
496
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