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年轻人饮酒的代谢组学特征。

The metabolomic signatures of alcohol consumption in young adults.

作者信息

Du Duc, Bruno Raimondo, Blizzard Leigh, Venn Alison, Dwyer Terence, Smith Kylie J, Magnussen Costan G, Gall Seana

机构信息

Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.

School of Medicine, University of Tasmania, Hobart, Australia.

出版信息

Eur J Prev Cardiol. 2020 May;27(8):840-849. doi: 10.1177/2047487319834767. Epub 2019 Mar 11.

Abstract

BACKGROUND

Metabolomic analysis may help us to understand the association between alcohol consumption and cardio-metabolic health. We aimed to: (i) replicate a previous study of alcohol consumption and metabolic profiles, (ii) examine associations between types of alcoholic beverages and metabolites and (iii) include potential confounders not examined in previous studies.

METHODS

Cross-sectional data of 1785 participants (age 26-36 years, 52% women) from the 2004-2006 Childhood Determinants of Adult Health study were used. Consumption of beer, wine and spirits was assessed by questionnaires. Metabolites were measured by a high-throughput nuclear magnetic resonance platform and multivariable linear regression examined their association with alcohol consumption (combined total and types) adjusted for covariates including socio-demographics, health behaviours and mental health.

RESULTS

Alcohol consumption was associated with 23 out of 37 lipids, 12 out of 16 fatty acids and six out of 20 low-molecular-weight metabolites independent of confounders with similar associations for combined total alcohol consumption and different types of alcohol. Many metabolites (lipoprotein lipids in high-density lipoprotein (HDL) subclasses, HDL cholesterol, apolipoprotein A-1, phosphotriglycerides, total fatty acids, monounsaturated fatty acids, omega-3 fatty acids) had positive linear associations with alcohol consumption but some showed negative linear (low-density lipoprotein particle size, omega-6 fatty acids ratio to total fatty acids, citrate) or U-shaped (lipoprotein lipids in very-low-density lipoprotein (VLDL) subclasses, VLDL triglycerides) associations.

CONCLUSIONS

Our results were similar to those of the only previous study. Associations with metabolites were similar for total and types of alcohol. Alcohol consumption in young adults is related to a diverse range of metabolomic signatures associated with benefits and harms to health.

摘要

背景

代谢组学分析可能有助于我们理解饮酒与心血管代谢健康之间的关联。我们的目标是:(i)重复先前关于饮酒与代谢谱的研究,(ii)研究酒精饮料类型与代谢物之间的关联,以及(iii)纳入先前研究未考察的潜在混杂因素。

方法

使用了来自2004 - 2006年成人健康儿童决定因素研究的1785名参与者(年龄26 - 36岁,52%为女性)的横断面数据。通过问卷评估啤酒、葡萄酒和烈酒的消费量。代谢物通过高通量核磁共振平台进行测量,并采用多变量线性回归分析其与饮酒量(总量和类型合并)之间的关联,同时对包括社会人口统计学、健康行为和心理健康等协变量进行了调整。

结果

饮酒与37种脂质中的23种、16种脂肪酸中的12种以及20种低分子量代谢物中的6种存在关联,独立于混杂因素,饮酒总量和不同类型酒精的关联相似。许多代谢物(高密度脂蛋白(HDL)亚类中的脂蛋白脂质、HDL胆固醇、载脂蛋白A - 1、磷酸甘油三酯、总脂肪酸、单不饱和脂肪酸、ω - 3脂肪酸)与饮酒量呈正线性关联,但有些呈现负线性(低密度脂蛋白颗粒大小、ω - 6脂肪酸与总脂肪酸的比率、柠檬酸盐)或U形(极低密度脂蛋白(VLDL)亚类中的脂蛋白脂质、VLDL甘油三酯)关联。

结论

我们的结果与之前唯一的一项研究相似。酒精总量和类型与代谢物的关联相似。年轻人饮酒与一系列不同的代谢组学特征相关,这些特征对健康既有益处也有危害。

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