Liu Huimin, Li Hai, Deng Guohong, Zheng Xin, Huang Yan, Chen Jinjun, Meng Zhongji, Gao Yanhang, Qian Zhiping, Liu Feng, Lu Xiaobo, Shi Yu, Shang Jia, Yan Huadong, Zheng Yubao, Shen Zixuan, Qiao Liang, Zhang Weituo, Wang Xianbo
Center of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Department of Traditional Medicine, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China.
Front Med (Lausanne). 2024 Mar 21;11:1307901. doi: 10.3389/fmed.2024.1307901. eCollection 2024.
A high aspartate aminotransferase/alanine aminotransferase (AST/ALT) ratio is associated with liver injury in liver disease; however, no data exist regarding its relationship with 90-day prognosis in patients with acute exacerbation of chronic liver disease.
In this study, 3,758 participants (955 with advanced fibrosis and 2,803 with cirrhosis) from the CATCH-LIFE cohort in China were included. The relationships between different AST/ALT ratios and the risk of adverse 90-day outcomes (death or liver transplantation) were determined in patients with cirrhosis or hepatitis B virus (HBV)-associated advanced fibrosis, respectively.
In the patients with HBV-associated advanced fibrosis, the risk of 90-day adverse outcomes increased with AST/ALT ratio; after adjusting for all confounding factors, the risk of adverse 90-day outcomes was the highest when AST/ALT ratio was more than 1.08 (OR = 6.91 [95% CI = 1.789-26.721], = 0.005), and the AST/ALT ratio of >1.9 accelerated the development of adverse outcomes. In patients with cirrhosis, an AST/ALT ratio > 1.38 increased the risk of adverse 90-day outcomes in all univariables (OR = 1.551 [95% CI = 1.216-1.983], < 0.001) and multivariable-adjusted analyses (OR = 1.847 [95% CI = 1.361-2.514], < 0.001), and an elevated AST/ALT ratio (<2.65) accelerated the incidence of 90-day adverse outcomes. An AST/ALT ratio of >1.38 corresponded with a more than 20% incidence of adverse outcomes in patients with cirrhosis.
The AST/ALT ratio is an independent risk factor for adverse 90-day outcomes in patients with cirrhosis and HBV-associated advanced fibrosis. The cutoff values of the AST/ALT ratio could help clinicians monitor the condition of patients when making clinical decisions.
天冬氨酸氨基转移酶/丙氨酸氨基转移酶(AST/ALT)比值升高与肝脏疾病中的肝损伤相关;然而,关于其与慢性肝病急性加重患者90天预后的关系尚无相关数据。
本研究纳入了中国CATCH-LIFE队列中的3758名参与者(955名有晚期纤维化,2803名有肝硬化)。分别在肝硬化患者或乙型肝炎病毒(HBV)相关晚期纤维化患者中,确定不同AST/ALT比值与90天不良结局(死亡或肝移植)风险之间的关系。
在HBV相关晚期纤维化患者中,90天不良结局的风险随AST/ALT比值升高而增加;在调整所有混杂因素后,当AST/ALT比值大于1.08时,90天不良结局的风险最高(OR = 6.91 [95% CI = 1.789 - 26.721],P = 0.005),且AST/ALT比值>1.9会加速不良结局的发展。在肝硬化患者中,AST/ALT比值>1.38在所有单变量分析(OR = 1.551 [95% CI = 1.216 - 1.983],P < 0.001)和多变量调整分析(OR = 1.847 [95% CI = 1.361 - 2.514],P < 0.001)中均增加了90天不良结局的风险,且升高的AST/ALT比值(<2.65)会加速90天不良结局的发生。AST/ALT比值>1.38对应肝硬化患者不良结局发生率超过20%。
AST/ALT比值是肝硬化和HBV相关晚期纤维化患者90天不良结局的独立危险因素。AST/ALT比值的临界值有助于临床医生在做出临床决策时监测患者病情。