Ten Berg P W, Shaffer J, Vliegenthart A D B, McCrae J, Sharkey N, Webb D J, Dear J W
a Centre for Cardiovascular Science, The Queen's Medical Research Institute , Edinburgh University , Edinburgh , UK.
b Qiagen , Frederick , MD , USA.
Biomarkers. 2018 Dec;23(8):781-786. doi: 10.1080/1354750X.2018.1499128. Epub 2018 Aug 23.
Circulating microRNAs represent a reservoir for biomarker discovery. Our objective was to profile the change in human circulating microRNA associated with recreational use of alcohol at a social event.
Blood was collected from healthy volunteers (N = 16) before and after recreational consumption of alcohol (ethanol). Biochemistry, hematology and ethanol measurements were performed. The change in the serum small RNA fraction was quantified by RNA sequencing.
Blood ethanol was undetectable at study entry in all subjects [<10 mg/dL]. After consuming alcohol the median concentration was 89 mg/dL [IQR: 71-138. Min-max 20-175]. There were no changes in biochemistry and hematology parameters. Serum RNA sequencing identified 1371 small RNA species (1305 microRNAs). There were significant increases [adjusted p-value <0.05, fold increase 2 or more] in 265 microRNAs, around a fifth of the total [median fold increase 2.3 [IQR: 2.1-2.5; Max: 3.7]]. miR-185-5p decreased following alcohol exposure [adjusted p-value <0.05, fold decrease 2 or more].
The microRNA composition of human serum is dynamic and environmental factors may have a significant impact. Within its context of use the fold change 'signal' of a microRNA must be large enough to negate the risk of false results due to background 'noise'.
循环微RNA是生物标志物发现的一个来源。我们的目标是描绘在社交活动中与娱乐性饮酒相关的人类循环微RNA的变化。
在健康志愿者(N = 16)娱乐性饮用酒精(乙醇)之前和之后采集血液。进行生物化学、血液学和乙醇测量。通过RNA测序对血清小RNA组分的变化进行定量。
在研究开始时所有受试者的血液乙醇均检测不到[<10mg/dL]。饮酒后,中位数浓度为89mg/dL[四分位间距:71 - 138。最小值 - 最大值20 - 175]。生物化学和血液学参数没有变化。血清RNA测序鉴定出1371种小RNA种类(1305种微RNA)。265种微RNA有显著增加[校正p值<0.05,增加倍数为2或更多],约占总数的五分之一[中位数增加倍数为2.3[四分位间距:2.1 - 2.5;最大值:3.7]]。酒精暴露后miR - 185 - 5p减少[校正p值<0.05,减少倍数为2或更多]。
人血清的微RNA组成是动态的,环境因素可能有重大影响。在其使用背景下,微RNA的倍数变化“信号”必须足够大,以消除由于背景“噪声”导致假结果的风险。