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The effects of alcohol consumption on flow‐mediated dilation in humans: A systematic review

Authors :
Mariann R. Piano
Chueh-Lung Hwang
Shane A. Phillips
Source :
Physiological Reports, Vol 9, Iss 10, Pp n/a-n/a (2021), Physiological Reports
Publication Year :
2021
Publisher :
Wiley, 2021.

Abstract

Changes in endothelial function may contribute to the positive and negative effects of alcohol consumption on cardiovascular conditions, such as hypertension and coronary artery disease. Numerous studies have used brachial artery flow‐mediated dilation (FMD) to examine the effects of alcohol consumption on endothelial function in humans. However, the findings are inconsistent and may be due to multiple factors such as heterogeneity in subject characteristics, the alcohol use pattern, and amount/dose of alcohol consumed. Therefore, the aim of this systematic review was to investigate the effect of alcohol consumption on brachial artery FMD in humans considering the above‐mentioned factors. This review found that while light to moderate alcohol consumption may have minimal effects on FMD, heavy alcohol consumption was associated with a decrease in FMD. However, most of the published studies included healthy, younger, and male individuals, limiting generalizability to other populations. Future studies should include more women, older subjects, and those from diverse and underrepresented backgrounds.<br />Numerous studies have used brachial FMD to examine the effects of alcohol consumption on endothelial function, but the findings are inconsistent. This may be due to multiple factors such as heterogeneity in subject characteristics (disease vs. healthy), alcohol type and amount, and measurement timing (acute vs. chronic consumption). Therefore, the purpose of this systematic review was to investigate the effect of alcohol consumption on FMD in human.

Details

Language :
English
Volume :
9
Issue :
10
Database :
OpenAIRE
Journal :
Physiological Reports
Accession number :
edsair.doi.dedup.....ccca9bf406ecaa66a3ccd16d62e78403