Hasanoglu Imran, Rivero-Juárez Antonio, Özkaya Şahin Gülşen
Department of Infectious Disease and Clinical Microbiology, Ankara Yildirim Beyazit University, Ankara Bilkent City Hospital, Ankara 06800, Türkiye.
Department of Infectious Diseases, Hospital Universitario Reina Sofia, Instituto Maimonides de Investigación Biomédica de Córdoba (IMIBIC), Universidad de Córdoba (UCO), 14071 Cordoba, Spain.
J Clin Med. 2025 May 14;14(10):3422. doi: 10.3390/jcm14103422.
The interplay between Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) and viral hepatitis, primarily hepatitis B virus (HBV) and hepatitis C virus (HCV), presents a complex challenge in managing chronic liver diseases. Recent epidemiological insights suggest an escalating prevalence of MASLD globally, attributed mainly to the obesity epidemic and associated metabolic disorders. Concurrently, chronic viral hepatitis remains a significant contributor to liver disease morbidity and mortality worldwide, despite advances in antiviral therapies. According to the World Health Organization (WHO) 2023 data, approximately 296 million people are living with chronic HBV infection (about 3.8% of the global population), and 58 million people with HCV infection (about 0.7%), together accounting for over 1.1 million deaths annually. The coexistence of MASLD and viral hepatitis presents a complex scenario in clinical outcomes, where the effects on liver health can vary. Although many studies highlight the potential for additive or synergistic worsening of liver conditions, leading to complications such as cirrhosis, liver failure, and HCC, the impact of HBV on MASLD is not consistent. Managing patients with dual MASLD and viral hepatitis is complex due to the interplay of metabolic and viral factors. Lifestyle modifications, including weight loss, dietary changes, and physical activity, are fundamental to MASLD management and help reduce fibrosis risk in viral hepatitis. This review examines the dual impact of MASLD and viral hepatitis on liver pathology and delineates shared pathophysiological mechanisms, including the influence on hepatic steatosis, inflammation, and fibrogenesis. It also discusses therapeutic strategies tailored to manage this comorbidity, emphasizing the need for an integrated care approach that addresses both metabolic dysfunctions and viral infection to optimize patient outcomes.
代谢功能障碍相关脂肪性肝病(MASLD)与病毒性肝炎,主要是乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)之间的相互作用,给慢性肝病的管理带来了复杂的挑战。最近的流行病学见解表明,全球范围内MASLD的患病率不断上升,这主要归因于肥胖流行和相关的代谢紊乱。与此同时,尽管抗病毒治疗取得了进展,但慢性病毒性肝炎仍然是全球肝病发病和死亡的重要原因。根据世界卫生组织(WHO)2023年的数据,约有2.96亿人患有慢性HBV感染(约占全球人口的3.8%),5800万人患有HCV感染(约占0.7%),每年总计导致超过110万人死亡。MASLD和病毒性肝炎的共存给临床结局带来了复杂的情况,对肝脏健康的影响可能各不相同。尽管许多研究强调了肝脏状况可能会因相加或协同作用而恶化,导致诸如肝硬化、肝衰竭和肝癌等并发症,但HBV对MASLD的影响并不一致。由于代谢和病毒因素的相互作用,管理同时患有MASLD和病毒性肝炎的患者很复杂。生活方式的改变,包括体重减轻、饮食变化和体育活动,对于MASLD的管理至关重要,并有助于降低病毒性肝炎的纤维化风险。本综述探讨了MASLD和病毒性肝炎对肝脏病理的双重影响,并阐述了共同的病理生理机制,包括对肝脂肪变性、炎症和纤维化形成的影响。它还讨论了针对这种合并症的治疗策略,强调需要一种综合护理方法,以解决代谢功能障碍和病毒感染问题,从而优化患者的治疗效果。