Eating and arterial endothelial function: a meta-analysis of the acute effects of meal consumption on flow-mediated dilation

被引:28
|
作者
Thom, N. J. [1 ]
Early, A. R. [2 ]
Hunt, B. E. [2 ]
Harris, R. A. [3 ]
Herring, M. P. [4 ,5 ]
机构
[1] Wheaton Coll, Dept Biol, 500 Coll Ave, Wheaton, IL 60187 USA
[2] Wheaton Coll, Appl Hlth Sci Dept, Wheaton, IL 60187 USA
[3] August Univ, Georgia Prevent Inst, Augusta, GA USA
[4] Univ Limerick, Dept Phys Educ & Sport Sci, Limerick, Ireland
[5] Univ Limerick, HRI, Limerick, Ireland
关键词
carbohydrate; fat; FMD; protein; POSTPRANDIAL LIPEMIA; OXIDATIVE STRESS; BRACHIAL-ARTERY; VASCULAR FUNCTION; RISK-FACTORS; DYSFUNCTION; HYPERTRIGLYCERIDEMIA; VASODILATION; GLUCOSE; WOMEN;
D O I
10.1111/obr.12454
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Given that endothelial dysfunction precedes atherosclerotic cardiovascular disease, exploring the parameters that modify postprandial flow-mediated dilation (FMD) is important for public health. The objectives of the study are to estimate the population effect of meal ingestion on FMD and to determine how the effect varied based on patient characteristics and modifiable methodological features. Articles published before June 2015 were located using MEDLINE, PubMed and Web of Science. One hundred fifty-four effects were derived from 78 articles involving 2,548 subjects were selected. Included articles required measurement of FMD in adults before and after meal ingestion. Effects were analysed using an unstandardized mean gain random effects model, and significant moderators were analysed using meta-regression. Meal consumption significantly reduced FMD by a heterogeneous mean effect size delta () of -2.03 (95% CI: [-2.28, -1.77]), an similar to tau 2% reduction in FMD. FMD reductions were larger among normal weight individuals, males, those with a cardio-metabolic disorder, those with elevated baseline FMD, and individuals with impaired glucose tolerance at baseline. Macronutrient meal ingestion significantly reduced FMD, an effect that was moderated by body mass index, sex and two-way interactions between disease status and both baseline FMD and baseline blood glucose levels.
引用
收藏
页码:1080 / 1090
页数:11
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