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膳食长链多不饱和脂肪酸的摄入量改变了 FADS 基因变异与 LDL-C 之间的关联。

Intake levels of dietary long-chain PUFAs modify the association between genetic variation in FADS and LDL-C.

机构信息

Diabetes and Cardiovascular Disease, Genetic Epidemiology, Department of Clinical Sciences in Malmö, Lund University, Sweden.

出版信息

J Lipid Res. 2012 Jun;53(6):1183-9. doi: 10.1194/jlr.P023721. Epub 2012 Mar 26.

Abstract

Polymorphisms of the FA desaturase (FADS) gene cluster have been associated with LDL, HDL, and triglyceride concentrations. Because FADS converts α-linolenic acid (ALA) and linoleic acid into PUFAs, we investigated the interaction between different PUFA intakes and the FADS polymorphism rs174547 (T>C) on fasting blood lipid and lipoprotein concentrations. We included 4,635 individuals (60% females, 45-68 years) from the Swedish population-based Malmö Diet and Cancer cohort. Dietary intakes were assessed by a modified diet history method including 7-day registration of cooked meals. The C-allele of rs174547 was associated with lower LDL concentration (P = 0.03). We observed significant interaction between rs174547 and long-chain ω-3 PUFA intakes on LDL (P = 0.01); the C-allele was only associated with lower LDL among individuals in the lowest tertile of long-chain ω-3 PUFA intakes (P < 0.001). In addition, significant interaction was observed between rs174547 and the ratio of ALA and linoleic FA intakes on HDL (P = 0.03). However, no significant associations between the C-allele and HDL were detected within the intake tertiles of the ratio. Our findings suggest that dietary intake levels of different PUFAs modify the associated effect of genetic variation in FADS on LDL and HDL.

摘要

脂肪酸去饱和酶(FADS)基因簇的多态性与 LDL、HDL 和甘油三酯浓度有关。因为 FADS 将α-亚麻酸(ALA)和亚油酸转化为多不饱和脂肪酸(PUFAs),所以我们研究了不同 PUFAs 摄入量与 FADS 基因 rs174547(T>C)多态性之间的相互作用,以及对空腹血脂和脂蛋白浓度的影响。我们纳入了来自瑞典基于人群的马尔默饮食与癌症队列的 4635 名个体(女性占 60%,年龄 45-68 岁)。饮食摄入量通过改良的饮食史法进行评估,包括 7 天的烹饪餐记录。rs174547 的 C 等位基因与 LDL 浓度较低相关(P = 0.03)。我们观察到 rs174547 与长链 ω-3 PUFA 摄入量之间存在显著的相互作用,对 LDL 有影响(P = 0.01);只有在长链 ω-3 PUFA 摄入量最低的个体中,C 等位基因才与 LDL 降低相关(P < 0.001)。此外,还观察到 rs174547 与 ALA 和亚油酸 FA 摄入量的比值与 HDL 之间存在显著的相互作用(P = 0.03)。然而,在比值的摄入量三分位内,未检测到 C 等位基因与 HDL 之间存在显著相关性。我们的研究结果表明,不同 PUFAs 的饮食摄入量水平改变了 FADS 基因变异与 LDL 和 HDL 相关的关联效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12f5/3351825/9ec2bcc523d4/1183fig1.jpg

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