Tillander Veronika, Holmer Magnus, Hagström Hannes, Petersson Sven, Brismar Torkel B, Stål Per, Lindqvist Catarina
Division of Clinical Chemistry, Cardio Metabolic Unit, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Unit of Gastroenterology and Hepatology, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Br J Nutr. 2024 Sep 18;132(4):1-13. doi: 10.1017/S0007114524001673.
Dietary fatty acids (FA) affect metabolic risk factors. The aim of this study was to explore if changes in dietary fat intake during energy restriction were associated with plasma FA composition. The study also investigated if these changes were associated with changes in liver fat, liver stiffness and plasma lipids among persons with non-alcoholic fatty liver disease. Dietary and plasma FA were investigated in patients with non-alcoholic fatty liver disease ( 48) previously enrolled in a 12-week-long open-label randomised controlled trial comparing two energy-restricted diets: a low-carbohydrate high-fat diet and intermittent fasting diet (5:2), to a control group. Self-reported 3 d food diaries were used for FA intake, and plasma FA composition was analysed using GC. Liver fat content and stiffness were measured by MRI and transient elastography. Changes in intake of total FA ( 0·41; = 0·005), SFA ( 0·38; = 0·011) and MUFA ( 0·42; = 0·004) were associated with changes in liver stiffness. Changes in plasma SFA ( 0·32; = 0·032) and C16 : 1-7 ( 0·33; = 0·028) were positively associated with changes in liver fat, while total -6 PUFA ( -0·33; = 0·028) and C20 : 4-6 ( -0·42; = 0·005) were inversely associated. Changes in dietary SFA, MUFA, cholesterol and C20:4 were positively associated with plasma total cholesterol and LDL-cholesterol. Modifying the composition of dietary fats during dietary interventions causes changes in the plasma FA profile in patients with non-alcoholic fatty liver disease. These changes are associated with changes in liver fat, stiffness, plasma cholesterol and TAG. Replacing SFA with PUFA may improve metabolic parameters in non-alcoholic fatty liver disease patients during weight loss treatment.
膳食脂肪酸(FA)会影响代谢风险因素。本研究的目的是探讨能量限制期间膳食脂肪摄入量的变化是否与血浆FA组成相关。该研究还调查了这些变化是否与非酒精性脂肪性肝病患者的肝脏脂肪、肝脏硬度和血脂变化相关。在先前参加一项为期12周的开放标签随机对照试验的48例非酒精性脂肪性肝病患者中,对膳食和血浆FA进行了研究,该试验将两种能量限制饮食(低碳水化合物高脂肪饮食和间歇性禁食饮食(5:2))与一个对照组进行比较。使用自我报告的3天食物日记来记录FA摄入量,并使用气相色谱法分析血浆FA组成。通过磁共振成像(MRI)和瞬时弹性成像测量肝脏脂肪含量和硬度。总FA摄入量的变化(β = 0.41;P = 0.005)、饱和脂肪酸(SFA)摄入量的变化(β = 0.38;P = 0.011)和单不饱和脂肪酸(MUFA)摄入量的变化(β = 0.42;P = 0.004)与肝脏硬度的变化相关。血浆SFA的变化(β = 0.32;P = 0.032)和C16:1-7的变化(β = 0.33;P = 0.028)与肝脏脂肪的变化呈正相关,而总ω-6多不饱和脂肪酸(PUFA)(β = -0.33;P = 0.028)和C20:4-6(β = -0.42;P = 0.005)呈负相关。膳食SFA、MUFA、胆固醇和C20:4的变化与血浆总胆固醇和低密度脂蛋白胆固醇呈正相关。在膳食干预期间改变膳食脂肪的组成会导致非酒精性脂肪性肝病患者血浆FA谱的变化。这些变化与肝脏脂肪、硬度、血浆胆固醇和甘油三酯(TAG)的变化相关。在减肥治疗期间,用PUFA替代SFA可能会改善非酒精性脂肪性肝病患者的代谢参数。