Hepatitis C virus and metabolic disorder interactions towards liver damage and atherosclerosis

被引:31
作者
Vespasiani-Gentilucci, Umberto [1 ]
Gallo, Paolo [1 ]
De Vincentis, Antonio [1 ]
Galati, Giovanni [1 ]
Picardi, Antonio [1 ]
机构
[1] Univ Campus Biomed Rome, Internal Med & Hepatol Unit, I-00128 Rome, Italy
关键词
Hepatitis C virus; Metabolism; Insulin resistance; Diabetes mellitus; Steatosis; Fibrosis; Atherosclerosis; Cardiovascular risk; SUSTAINED VIROLOGICAL RESPONSE; ACTIVATED-RECEPTOR-ALPHA; TRIGLYCERIDE TRANSFER PROTEIN; TYPE-2; DIABETES-MELLITUS; CORONARY-ARTERY-DISEASE; CHRONIC VIRAL-HEPATITIS; POPULATION-BASED COHORT; NECROSIS-FACTOR-ALPHA; CHRONIC HCV INFECTION; INCREASED ALL-CAUSE;
D O I
10.3748/wjg.v20.i11.2825
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis C virus (HCV) is one of the main causes of liver disease worldwide, and alterations of glucose metabolism have reached pandemic proportions in western countries. However, the frequent coexistence between these two conditions is more than simply coincidental, since HCV can induce insulin resistance through several mechanisms. Indeed, the virus interferes with insulin signaling both directly and indirectly, inducing the production of pro-inflammatory cytokines. Furthermore, the entire viral life cycle has strict interconnections with lipid metabolism, and HCV is responsible for a "viral" steatosis which is frequently superimposed to a "metabolic" one. Several evidences suggest that HCV-induced metabolic disorders contribute both to the evolution of liver fibrosis and, likely, to the progression of the other disorders which are typically associated with altered metabolism, in particular atherosclerosis. In the present review, we will examine in depth the links between HCV infection and insulin resistance, liver steatosis and diabetes, and analyze the impact of these interactions on the progression of liver fibrosis and atherosclerosis. Special attention will be focused on the highly debated topic of the relationship between HCV infection and cardiovascular disease. The available clinical literature on this item will be broadly reviewed and all the mechanisms possibly implied will be discussed. (c) 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
引用
收藏
页码:2825 / 2838
页数:14
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