Kim Yun
Hanyang Medicine-Engineering-Bio Collaborative & Comprehensive Center for Drug Development, Hanyang University, Seoul 04763, Korea.
Life (Basel). 2021 Mar 17;11(3):250. doi: 10.3390/life11030250.
Sarcopenia is characterized by a skeletal muscle disorder with progressive and generalized loss of muscle mass and function, and it increases the risk of adverse outcomes with considerable prevalence in patients with chronic liver disease. Sarcopenia in chronic liver disease underlies complicated and multifactorial mechanisms for pathogenesis, including alterations in protein turnover, hyperammonemia, energy disposal, hormonal changes, and chronic inflammation. The key contribution to sarcopenia in patients with chronic liver diseases can be the hyperammonemia-induced upregulation of myostatin, which causes muscle atrophy via the expression of atrophy-related genes. Several clinical studies on emerging treatment options for sarcopenia have been reported, but only a few have focused on patients with chronic liver diseases, with mostly nutritional and behavioral interventions being carried out. The inhibition of the myostatin-activin receptor signaling pathway and hormonal therapy might be the most promising therapeutic options in combination with an ammonia-lowering approach in sarcopenic patients with chronic liver diseases. This review focuses on current and emerging treatment options for sarcopenia in chronic liver diseases with underlying mechanisms to counteract this condition.
肌肉减少症的特征是一种骨骼肌疾病,伴有肌肉质量和功能的进行性和全身性丧失,并且它增加了慢性肝病患者不良结局的风险,其患病率相当高。慢性肝病中的肌肉减少症是复杂且多因素的发病机制的基础,包括蛋白质周转改变、高氨血症、能量代谢、激素变化和慢性炎症。慢性肝病患者肌肉减少症的关键因素可能是高氨血症诱导的肌肉生长抑制素上调,其通过与萎缩相关基因的表达导致肌肉萎缩。已经报道了几项关于肌肉减少症新兴治疗选择的临床研究,但只有少数研究关注慢性肝病患者,主要进行的是营养和行为干预。在患有慢性肝病的肌肉减少症患者中,抑制肌肉生长抑制素-激活素受体信号通路和激素治疗可能是结合降氨方法最有前景的治疗选择。本综述重点关注慢性肝病中肌肉减少症的当前和新兴治疗选择以及对抗这种情况的潜在机制。