Elkhattib Ismail, Raafat Kareem Wael, Elsayed Basant, Elnaggar Mohamed
Division of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha, NE 68105, United States.
Faculty of Medicine, Suez Canal University, Ismailia 41522, Egypt.
World J Hepatol. 2025 Aug 27;17(8):108678. doi: 10.4254/wjh.v17.i8.108678.
Hepatitis C virus (HCV) infection has been increasingly associated with cardiovascular complications, particularly atherosclerosis and cardiomyopathy, in addition to its primary hepatic effects. Studies indicate a higher prevalence of carotid atherosclerosis in patients with chronic hepatitis C infection, with viral load and steatosis emerging as independent risk factors. HCV-related atherosclerosis appears to develop through complex processes involving endothelial dysfunction, inflammation, oxidative stress, and immune dysregulation. Key cytokines, including tumor necrosis factor-alpha and interleukin-6, increase inflammatory responses, while oxidative stress markers, such as malondialdehyde, are associated with an increased risk of atherogenesis. In addition, HCV infection has been linked to cardiomyopathy. Direct viral effects, including HCV replication within cardiomyocytes and cytotoxicity induced by viral proteins, lead to myocardial injury and functional decline. Indirectly, HCV triggers immune-mediated damage, with heightened pro-inflammatory cytokines exacerbating cardiomyocyte apoptosis and fibrosis. Furthermore, HCV infection promotes a procoagulant imbalance, as evidenced by elevated factor VIII levels and thrombin potential, contributing to the increased cardiovascular risk. While substantial evidence indicates a relationship between HCV and cardiovascular disease, further research is needed to establish causality and guide therapeutic interventions.
丙型肝炎病毒(HCV)感染除了对肝脏产生原发性影响外,还越来越多地与心血管并发症相关,尤其是动脉粥样硬化和心肌病。研究表明,慢性丙型肝炎感染患者颈动脉粥样硬化的患病率较高,病毒载量和脂肪变性已成为独立的危险因素。HCV相关的动脉粥样硬化似乎是通过涉及内皮功能障碍、炎症、氧化应激和免疫失调的复杂过程发展而来。关键细胞因子,包括肿瘤坏死因子-α和白细胞介素-6,会增加炎症反应,而氧化应激标志物,如丙二醛,与动脉粥样硬化风险增加有关。此外,HCV感染与心肌病有关。直接的病毒效应,包括HCV在心肌细胞内复制以及病毒蛋白诱导的细胞毒性,会导致心肌损伤和功能下降。间接而言,HCV引发免疫介导的损伤,促炎细胞因子水平升高会加剧心肌细胞凋亡和纤维化。此外,HCV感染会促进促凝失衡,凝血因子VIII水平和凝血酶潜力升高就是证明,这会增加心血管疾病风险。虽然大量证据表明HCV与心血管疾病之间存在关联,但仍需要进一步研究来确定因果关系并指导治疗干预。