Alsharari Zayed D, Leander Karin, Sjögren Per, Carlsson Axel, Cederholm Tommy, de Faire Ulf, Hellenius Mai-Lis, Marklund Matti, Risérus Ulf
Department of Public Health and Caring Sciences, Clinical Nutrition and Metabolism, Uppsala University, Box 564, 75122, Uppsala, Sweden.
Unit of Cardiovascular Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Eur J Nutr. 2020 Aug;59(5):2089-2097. doi: 10.1007/s00394-019-02058-6. Epub 2019 Jul 26.
Fatty acid composition in blood and adipose tissue (AT) is a useful biomarker of dietary fat quality. However, circulating saturated fatty acids (SFA) and monounsaturated fatty acids (MUFA) have been proposed to also reflect carbohydrate-induced de novo lipogenesis (DNL) and stearoyl-CoA desaturase (SCD) activity. We aimed to test the hypothesis that high carbohydrate intake is related to SFA and MUFA in serum or AT in a Swedish population.
Fatty acid composition was measured in serum phospholipids (PL) and AT by gas chromatography in 63-year-old men (n = 299). Carbohydrate and alcohol intake was assessed (validated 7-day food records) in relation to total SFA, 16:0 (palmitate), 16:1 (palmitoleate), and estimated SCD activity (16:1n-7/16:0-ratio) in serum PL and in AT, respectively.
Total carbohydrate intake was inversely associated with 16:0 in PL (P = 0.005), independently of BMI. Disaccharides were non-linearly (restricted cubic splines) and weakly associated with 16:1 and SCD activity in PL (nonlinear trend, P ≤ 0.02) but not AT. Carbohydrate intake and SCD expression were not associated (P ≥ 0.08, n = 81). Alcohol intake was, however, linearly associated with 16:0 in PL (P < 0.001), and with 16:1 (P < 0.001) and SCD activity (P ≤ 0.005) in both PL and AT.
Higher carbohydrate intake from sugar-rich foods or beverages was not clearly reflected by higher SFA or SCD activity in serum PL or AT. Alcohol was, however, associated with higher SFA and MUFA.
血液和脂肪组织(AT)中的脂肪酸组成是饮食脂肪质量的有用生物标志物。然而,有人提出循环饱和脂肪酸(SFA)和单不饱和脂肪酸(MUFA)也反映了碳水化合物诱导的从头脂肪生成(DNL)和硬脂酰辅酶A去饱和酶(SCD)活性。我们旨在检验高碳水化合物摄入量与瑞典人群血清或脂肪组织中SFA和MUFA相关的假设。
通过气相色谱法测定了299名63岁男性血清磷脂(PL)和脂肪组织中的脂肪酸组成。分别评估了碳水化合物和酒精摄入量(经过验证的7天食物记录)与血清PL和脂肪组织中总SFA、16:0(棕榈酸)、16:1(棕榈油酸)以及估计的SCD活性(16:1n-7/16:0比值)的关系。
总碳水化合物摄入量与PL中的16:0呈负相关(P = 0.005),独立于BMI。双糖与PL中的16:1和SCD活性呈非线性(受限立方样条)且弱相关(非线性趋势,P≤0.02),但与脂肪组织无关。碳水化合物摄入量与SCD表达无关联(P≥0.08,n = 81)。然而,酒精摄入量与PL中的16:0呈线性相关(P < 0.001),与PL和脂肪组织中的16:1(P < 0.001)和SCD活性(P≤0.005)均呈线性相关。
富含糖的食物或饮料中较高的碳水化合物摄入量在血清PL或脂肪组织中并未明显反映为较高的SFA或SCD活性。然而,酒精与较高的SFA和MUFA相关。