Dong Qingfu, Bao Haolin, Wang Jiangang, Shi Wujiang, Zou Xinlei, Sheng Jialin, Gao Jianjun, Guan Canghai, Xia Haoming, Li Jinglin, Kang Pengcheng, Xu Yi, Cui Yunfu, Zhong Xiangyu
Department of Hepatopancreatobiliary Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Department of General Surgery, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Front Med (Lausanne). 2023 Apr 20;10:1120621. doi: 10.3389/fmed.2023.1120621. eCollection 2023.
In recent years, the prevalence of metabolic-associated fatty liver disease (MAFLD) has reached pandemic proportions as a leading cause of liver fibrosis worldwide. However, the stage of liver fibrosis is associated with an increased risk of severe liver-related and cardiovascular events and is the strongest predictor of mortality in MAFLD patients. More and more people believe that MAFLD is a multifactorial disease with multiple pathways are involved in promoting the progression of liver fibrosis. Numerous drug targets and drugs have been explored for various anti-fibrosis pathways. The treatment of single medicines is brutal to obtain satisfactory results, so the strategies of multi-drug combination therapies have attracted increasing attention. In this review, we discuss the mechanism of MAFLD-related liver fibrosis and its regression, summarize the current intervention and treatment methods for this disease, and focus on the analysis of drug combination strategies for MAFLD and its subsequent liver fibrosis in recent years to explore safer and more effective multi-drug combination therapy strategies.
近年来,作为全球肝纤维化的主要原因,代谢相关脂肪性肝病(MAFLD)的患病率已达到大流行程度。然而,肝纤维化阶段与严重肝脏相关事件和心血管事件的风险增加相关,并且是MAFLD患者死亡率的最强预测因素。越来越多的人认为MAFLD是一种多因素疾病,有多种途径参与促进肝纤维化的进展。针对各种抗纤维化途径已经探索了众多药物靶点和药物。单一药物治疗很难获得满意的效果,因此多药联合治疗策略越来越受到关注。在本综述中,我们讨论MAFLD相关肝纤维化及其消退的机制,总结该疾病目前的干预和治疗方法,并重点分析近年来MAFLD及其后续肝纤维化的药物联合策略,以探索更安全、更有效的多药联合治疗策略。