Taneja Sunil, Roy Akash, Duseja Ajay
Department of Hepatology, Postgraduate Institute on Medical Education & Research, Chandigarh, India.
Institute of Gastrosciences and Liver Transplantation Apollo Multispeciality Hospitals, Kolkata, India.
J Clin Exp Hepatol. 2023 Sep-Oct;13(5):835-840. doi: 10.1016/j.jceh.2023.03.013. Epub 2023 Apr 3.
Non-alcoholic fatty liver disease (NAFLD) has emerged as one of the common causes of cirrhosis and hepatocellular carcinoma (HCC) and is a leading indication for liver transplantation (LT). Patients with NAFLD-related cirrhosis and HCC are at high risk for the development of recurrent NAFLD after LT. NAFLD can also develop post-transplantation in patients subjected to LT for other indications. Besides the pretransplant presence of various components of metabolic syndrome (MS) use of immunosuppressive agents in the post-LT setting forms one of the major drivers for the development of post-LT NAFLD. Individual components of conventional immunosuppressive regimens (corticosteroids, calcineurin inhibitors, and m-TOR inhibitors) are all implicated in the development of post-LT metabolic derangement and follow unique mechanisms of action and degree of disturbances. The development of cardiovascular risk is associated with post-LT NAFLD, although graft outcomes do not seem to be influenced only by the presence of post-LT NAFLD. Measures in consonance with the management of NAFLD, in general, including lifestyle modifications and control of metabolic risk factors, hold true for post-LT NAFLD. Tailoring immunosuppression strategies with early corticosteroid withdrawal and calcineurin inhibitor minimization balancing against the risk of graft rejection constitutes important nuances in the individualized management of post-LT NAFLD.
非酒精性脂肪性肝病(NAFLD)已成为肝硬化和肝细胞癌(HCC)的常见病因之一,并且是肝移植(LT)的主要适应证。患有NAFLD相关肝硬化和HCC的患者在LT后发生复发性NAFLD的风险很高。NAFLD也可在因其他适应证接受LT的患者中于移植后发生。除了移植前存在代谢综合征(MS)的各种组分外,LT后使用免疫抑制剂是LT后NAFLD发生的主要驱动因素之一。传统免疫抑制方案的各个组分(皮质类固醇、钙调神经磷酸酶抑制剂和m-TOR抑制剂)均与LT后代谢紊乱的发生有关,并遵循独特的作用机制和干扰程度。心血管风险的发生与LT后NAFLD相关,尽管移植结局似乎并不仅受LT后NAFLD存在的影响。一般而言,与NAFLD管理相一致的措施,包括生活方式改变和代谢危险因素控制,同样适用于LT后NAFLD。在个体化管理LT后NAFLD时,采用早期停用皮质类固醇和尽量减少钙调神经磷酸酶抑制剂的免疫抑制策略,同时平衡移植排斥风险,构成了重要的细微差别。