Research Centre, CHU Sainte-Justine, Université de Montreal, Montreal, Quebec, Canada; Department of Nutrition, Université de Montreal, Montreal, Quebec, Canada; Institute of Nutraceuticals and Functional foods, Université Laval, Quebec, Quebec, Canada.
Research Centre, CHU Sainte-Justine, Université de Montreal, Montreal, Quebec, Canada; Department of Pediatrics, Université de Montreal, Montreal, Quebec, Canada.
J Nutr Biochem. 2018 Aug;58:28-36. doi: 10.1016/j.jnutbio.2018.03.025. Epub 2018 Apr 10.
Although n-3 polyunsaturated fatty acids (PUFA) revealed promising therapeutic results in non-alcoholic fatty liver disease (NAFLD), which is considered as the most prevalent cause of chronic hepatic disease, inconsistencies are calling for further confirmatory trials to demonstrate therapeutic efficacy and safety. The study, registered as NCT02201160 on www.clinicaltrials.gov, was designed to compare two groups of NAFLD with a different severity, and to evaluate the efficacy of n-3 PUFA supplementation. Twenty young male participants of French Canadian origin with NAFLD were enrolled and classified into moderate (mNAFLD) and severe (sNAFLD) fatty liver groups, according to transaminase levels, ultrasonography, NAFLD Activity Score and Fatty Liver Index (FLI). The sNAFLD patients were assigned to consume 2 g of n-3 PUFA for 6 months. sNAFLD patients displayed higher insulinemia, insulin resistance (IR), oxidative stress (OxS), systolic blood pressure and the risk lipid indicators of cardiovascular diseases. Supplementation of n-3 PUFA for 6 months resulted in a significant increase in concentrations of eicosapentaenoic and docosahexaenoic acids in red blood cells along with an attenuation of hepatic steatosis as reflected by the reduction of the FLI, ALT and ALT/AST ratio. Moreover, the n-3 PUFA improved the lipid profile and carotid intima-media thickness, while reducing metabolic and OxS markers as well as raising adiponectin. In conclusion, NAFLD severity was essentially related to IR. Treatment with n-3 PUFA has an evidently beneficial effect on liver steatosis and related metabolic abnormalities. Furthermore, the cross association of omega-3 index with cardiometabolic markers may serve as a predictor for cardiovascular risk disorders in NAFLD.
尽管 n-3 多不饱和脂肪酸(PUFA)在非酒精性脂肪性肝病(NAFLD)中显示出有希望的治疗效果,NAFLD 被认为是最常见的慢性肝病病因,但结果的不一致性仍需要进一步的确认性试验来证明其治疗效果和安全性。这项研究在 www.clinicaltrials.gov 上注册为 NCT02201160,旨在比较两组不同严重程度的 NAFLD,并评估 n-3 PUFA 补充的疗效。20 名具有 NAFLD 的法裔加拿大男性青年参与者被纳入研究,并根据转氨酶水平、超声、NAFLD 活动评分和脂肪肝指数(FLI)将其分为中度(mNAFLD)和重度(sNAFLD)脂肪肝组。sNAFLD 患者被分配在 6 个月内摄入 2 克 n-3 PUFA。sNAFLD 患者表现出更高的胰岛素血症、胰岛素抵抗(IR)、氧化应激(OxS)、收缩压和心血管疾病的风险脂质指标。补充 n-3 PUFA 6 个月后,红细胞中二十碳五烯酸和二十二碳六烯酸的浓度显著增加,同时 FLI、ALT 和 ALT/AST 比值降低,表明肝脂肪变性减轻。此外,n-3 PUFA 改善了血脂谱和颈动脉内膜中层厚度,同时降低了代谢和 OxS 标志物,并提高了脂联素水平。总之,NAFLD 的严重程度与 IR 密切相关。n-3 PUFA 治疗对肝脂肪变性和相关代谢异常具有明显的有益作用。此外,ω-3 指数与心血管代谢标志物的交叉关联可能可作为 NAFLD 心血管风险障碍的预测因子。