Division of Gastroenterology, University of Washington, Seattle, Washington, United States of America.
Division of Gastroenterology, Cedar Sinai School of Medicine, Los Angeles, California, United States of America.
PLoS One. 2023 Apr 25;18(4):e0284739. doi: 10.1371/journal.pone.0284739. eCollection 2023.
Branched chain amino acids (BCAA) supplementation may reduce the incidence of liver failure and hepatocellular carcinoma in patients with cirrhosis. We aimed to determine whether long-term dietary intake of BCAA is associated with liver-related mortality in a well-characterized cohort of North American patients with advanced fibrosis or compensated cirrhosis. We performed a retrospective cohort study using extended follow-up data from the Hepatitis C Antiviral Long-term Treatment against Cirrhosis (HALT-C) Trial. The analysis included 656 patients who completed two Food Frequency Questionnaires. The primary exposure was BCAA intake measured in grams (g) per 1000 kilocalories (kcal) of energy intake (range 3.0-34.8 g/1000 kcal). During a median follow-up of 5.0 years, the incidence of liver-related death or transplantation was not significantly different among the four quartiles of BCAA intake before and after adjustment of confounders (AHR 1.02, 95% CI 0.81-1.27, P-value for trend = 0.89). There remains no association when BCAA was modeled as a ratio of BCAA to total protein intake or as absolute BCAA intake. Finally, BCAA intake was not associated with the risk of hepatocellular carcinoma, encephalopathy or clinical hepatic decompensation. We concluded that dietary BCAA intake was not associated with liver-related outcomes in HCV-infected patients with advanced fibrosis or compensated cirrhosis. The precise effect of BCAA in patients with liver disease warrants further study.
支链氨基酸(BCAA)补充可能会降低肝硬化患者肝衰竭和肝细胞癌的发生率。我们旨在确定长期摄入 BCAA 是否与北美患有晚期纤维化或代偿性肝硬化的患者的肝脏相关死亡率相关。我们使用丙型肝炎抗病毒长期治疗肝硬化(HALT-C)试验的扩展随访数据进行了回顾性队列研究。分析包括完成两份食物频率问卷的 656 名患者。主要暴露是每 1000 千卡能量摄入中 BCAA 的摄入量(范围为 3.0-34.8 g/1000 kcal),以克(g)为单位测量。在中位数为 5.0 年的随访期间,在调整混杂因素后,BCAA 摄入量的四个四分位数之间,肝脏相关死亡或移植的发生率没有显着差异(AHR 1.02,95%CI 0.81-1.27,趋势检验 P 值=0.89)。当将 BCAA 建模为 BCAA 与总蛋白质摄入量的比值或作为绝对 BCAA 摄入量时,仍然没有关联。最后,BCAA 摄入量与肝细胞癌、肝性脑病或临床肝功能失代偿的风险无关。我们的结论是,在患有晚期纤维化或代偿性肝硬化的 HCV 感染患者中,饮食 BCAA 摄入与肝脏相关结局无关。BCAA 在肝病患者中的确切作用需要进一步研究。