Metabolic Dysfunction-Associated Steatotic Liver Disease in Chronic Hepatitis C Virus Infection: From Basics to Clinical and Nutritional Management.

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Clinics and Practice Pub Date : 2024-11-24 DOI:10.3390/clinpract14060200
Karina Gonzalez-Aldaco, Luis A Torres-Reyes, Claudia Ojeda-Granados, Leonardo Leal-Mercado, Sonia Roman, Arturo Panduro
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Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is closely associated with obesity and other cardiometabolic risk factors. MASLD has rapidly become the most common cause of liver disease worldwide, currently affecting 38% of the global population. Excess weight causes chronic inflammation and the activation of different pathways involved in liver damage. MASLD can progress from simple steatosis to steatohepatitis, giving way to its inflammatory component, metabolic dysfunction-associated steatohepatitis (MASH), previously recognized as non-alcoholic steatosis hepatitis (NASH). Chronic hepatitis C virus (HCV) infection remains a significant challenge to liver health as it triggers hepatic inflammation, metabolic disruption, and hepatic steatosis. The convergence of MASLD and chronic HCV infection can significantly alter the course of liver disease and accelerate the progression to severe liver damage. Currently, HCV treatment has a high cure rate. However, in patients who achieve a sustained virological response after treatment with direct-acting antivirals, weight gain, and excessive calorie intake may contribute to increased liver steatosis and a higher risk of liver disease progression. Therefore, the effective clinical and nutritional management of HCV patients, both before and after viral eradication, is crucial to reducing the risk of death from hepatocellular carcinoma. Understanding the complex interactions between MASLD and HCV infection is crucial for managing these patients appropriately. Herein, host and viral mechanisms inducing liver damage during the coexistence of MASLD and HCV infection are described, and their therapeutic and dietary management are discussed.

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慢性丙型肝炎病毒感染的代谢功能障碍相关性脂肪肝:从基础知识到临床和营养管理。
代谢功能障碍相关性脂肪性肝病(MASLD)与肥胖和其他心脏代谢风险因素密切相关。代谢功能障碍相关性脂肪性肝病已迅速成为全球最常见的肝病,目前影响着全球 38% 的人口。体重过重会导致慢性炎症,并激活参与肝损伤的不同途径。MASLD 可从单纯性脂肪变性发展为脂肪性肝炎,进而发展为其炎症组成部分--代谢功能障碍相关性脂肪性肝炎(MASH),即以前所称的非酒精性脂肪变性性肝炎(NASH)。由于慢性丙型肝炎病毒(HCV)感染会引发肝脏炎症、代谢紊乱和肝脂肪变性,因此它仍然是肝脏健康的重大挑战。MASLD和慢性丙型肝炎病毒(HCV)感染并发可显著改变肝病的病程,加速肝脏严重受损。目前,HCV 治疗的治愈率很高。然而,在使用直接作用抗病毒药物治疗后获得持续病毒学应答的患者中,体重增加和热量摄入过多可能会导致肝脏脂肪变性加重,肝病进展的风险更高。因此,在病毒根除前后对 HCV 患者进行有效的临床和营养管理对于降低肝细胞癌的死亡风险至关重要。了解 MASLD 和 HCV 感染之间复杂的相互作用对于适当管理这些患者至关重要。本文阐述了在 MASLD 和 HCV 感染并存期间诱发肝损伤的宿主和病毒机制,并讨论了其治疗和饮食管理。
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来源期刊
Clinics and Practice
Clinics and Practice MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
4.30%
发文量
91
审稿时长
10 weeks
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