Shanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai 200437, China.
Key Laboratory of Public Health Safety, Department of Epidemiology, School of Public Health, Ministry of Education, Fudan University, Shanghai 200437, China.
Nutrients. 2024 Jul 17;16(14):2295. doi: 10.3390/nu16142295.
The role of serum branched-chain amino acids (BCAAs) in long-term liver cirrhosis complication events remains unclear. We aimed to evaluate the associations between serum BCAAs and the risk of liver-related events.
We included a total of 64,005 participants without liver cirrhosis complication events at baseline from the UK Biobank. Cox proportional hazards regression models were utilized to estimate multivariable hazard ratios (HRs) and 95% CIs for the incidence of liver cirrhosis complication events, adjusting for potential confounders, including sociodemographic and lifestyle factors. Relationships between serum BCAAs and liver cirrhosis complications were examined using nonparametrically restricted cubic spline regression.
During a median follow-up of 12.7 years, 583 participants developed liver cirrhosis complication events. The multivariable Cox regression model suggested that total BCAAs (HR = 0.88, 95% CI 0.82-0.95), serum leucine (HR = 0.88, 95% CI 0.81-0.95), serum isoleucine (HR = 0.88, 95% CI 0.82-0.96), and serum valine (HR = 0.87, 95% CI 0.82-0.96) were all independent protective factors for liver cirrhosis complications after adjustment for sociodemographic and lifestyle factors. Cox models with restricted cubic splines showed U-shaped associations between serum valine and liver cirrhosis complication incidence. Serum total BCAA and isoleucine concentrations might reduce the risk of liver cirrhosis complications by raising the risk of (type 2 diabetes mellitus) T2DM.
Lower serum BCAA levels exacerbate the long-term risk of liver cirrhosis complications. Future studies should confirm these findings and identify the biological pathways of these associations.
血清支链氨基酸(BCAAs)在长期肝硬化并发症事件中的作用尚不清楚。本研究旨在评估血清 BCAAs 与肝脏相关事件风险之间的关联。
本研究共纳入了英国生物库中基线时无肝硬化并发症事件的 64005 名参与者。采用 Cox 比例风险回归模型,估计多变量风险比(HR)和 95%置信区间(CI),以评估血清 BCAAs 与肝硬化并发症事件发生风险之间的关系,调整了潜在的混杂因素,包括社会人口统计学和生活方式因素。使用非参数限制立方样条回归来检查血清 BCAAs 与肝硬化并发症之间的关系。
在中位随访 12.7 年期间,583 名参与者发生了肝硬化并发症事件。多变量 Cox 回归模型表明,总 BCAAs(HR=0.88,95%CI 0.82-0.95)、血清亮氨酸(HR=0.88,95%CI 0.81-0.95)、血清异亮氨酸(HR=0.88,95%CI 0.82-0.96)和血清缬氨酸(HR=0.87,95%CI 0.82-0.96)均为校正社会人口统计学和生活方式因素后肝硬化并发症的独立保护因素。限制立方样条 Cox 模型显示血清缬氨酸与肝硬化并发症发生率之间呈 U 型关联。血清总 BCAA 和异亮氨酸浓度可能通过增加(2 型糖尿病)T2DM 的风险来降低肝硬化并发症的风险。
较低的血清 BCAAs 水平会加重长期肝硬化并发症的风险。未来的研究应证实这些发现并确定这些关联的生物学途径。