Shanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China; Department of Epidemiology, School of Public Health, Key Laboratory of Public Health Safety (Fudan University), Ministry of Education, Fudan University, Shanghai, China.
State Key Laboratory of Genetic Engineering, Human Phenome Institute, and School of Life Sciences, Fudan University, Shanghai, China; Fudan University Taizhou Institute of Health Sciences, Taizhou, China.
Clin Nutr. 2024 Sep;43(9):2083-2091. doi: 10.1016/j.clnu.2024.07.027. Epub 2024 Jul 31.
BACKGROUND & AIMS: The role of circulating polyunsaturated fatty acids (PUFAs) in preventing liver cirrhosis complications remains unclear.
Between 2006 and 2010, 273,834 UK Biobank participants with plasma PUFA quantification data were enrolled and followed up until October 31, 2022. Plasma PUFAs were quantified using a high-throughput nuclear magnetic resonance-based metabolic profiling platform. Liver cirrhosis complications were defined as hospitalization for liver cirrhosis or presentation with hepatocellular carcinoma.
During a median follow-up of 13.9 years, 2026 participants developed liver cirrhosis complications. Total plasma PUFAs, omega-3 PUFAs, docosahexaenoic acid (DHA), omega-6 PUFAs, and linoleic acid (LA) were inversely associated with the risk of liver cirrhosis complications, whereas the plasma omega-6/omega-3 ratio was positively associated. Nonparametrically restricted cubic spline regression showed nonlinear associations of plasma PUFAs with liver cirrhosis complications. The inflection points were 4.78 mmol/L for total PUFAs, 0.73 mmol/L for omega-3 PUFAs, 0.25 mmol/L for DHA, 4.07 mmol/L for omega-6 PUFAs, and 2.99 mmol/L for LA. Plasma omega-3 PUFAs were negatively associated with the risk of liver cirrhosis complications when omega-3 PUFAs were <0.73 mmol/L (adjusted hazard ratio [HR], 0.11 [0.08-0.16]), whereas the association was inverted when omega-3 PUFAs were ≥0.73 mmol/L (adjusted HR, 1.87 [1.20-2.92]).
The protective effect of plasma omega-3 PUFAs on liver cirrhosis complications is reversed after passing the corresponding inflection point, suggesting an optimal dietary omega-3 PUFA supplementation dose.
循环多不饱和脂肪酸(PUFAs)在预防肝硬化并发症中的作用尚不清楚。
2006 年至 2010 年间,共纳入 273834 名英国生物库参与者,这些参与者均有血浆 PUFAs 定量数据,并随访至 2022 年 10 月 31 日。采用高通量基于核磁共振的代谢谱分析平台定量检测血浆 PUFAs。肝硬化并发症定义为因肝硬化住院或出现肝细胞癌。
在中位随访 13.9 年期间,2026 名参与者发生了肝硬化并发症。总血浆 PUFAs、ω-3 PUFAs、二十二碳六烯酸(DHA)、ω-6 PUFAs 和亚油酸(LA)与肝硬化并发症风险呈负相关,而血浆 ω-6/ω-3 比值与肝硬化并发症风险呈正相关。非参数限制性立方样条回归显示,血浆 PUFAs 与肝硬化并发症之间存在非线性关联。拐点为总 PUFAs 4.78mmol/L、ω-3 PUFAs 0.73mmol/L、DHA 0.25mmol/L、ω-6 PUFAs 4.07mmol/L 和 LA 2.99mmol/L。当 ω-3 PUFAs<0.73mmol/L 时,血浆 ω-3 PUFAs 与肝硬化并发症风险呈负相关(调整后的危险比 [HR],0.11 [0.08-0.16]),而当 ω-3 PUFAs≥0.73mmol/L 时,相关性则相反(调整后的 HR,1.87 [1.20-2.92])。
当血浆 ω-3 PUFAs 超过相应拐点时,其对肝硬化并发症的保护作用会发生逆转,提示存在最佳的膳食 ω-3 PUFAs 补充剂量。