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血液中的磷脂酰乙醇作为健康志愿者乙醇摄入的标志物:与其他标志物的比较。

Phosphatidylethanol in blood as a marker of ethanol consumption in healthy volunteers: comparison with other markers.

作者信息

Varga A, Hansson P, Lundqvist C, Alling C

机构信息

Department of Medical Neurochemistry, Institute of Laboratory Medicine, Lund University, Sweden.

出版信息

Alcohol Clin Exp Res. 1998 Nov;22(8):1832-7.

PMID:9835304
Abstract

Phosphatidylethanol is a "pathological" phospholipid, formed via the action of phospholipase D only in the presence of ethanol. The present study was made to elucidate how different levels and patterns of alcohol intake affect blood levels of phosphatidylethanol in comparison with other markers of abuse. We used a new HPLC-evaporative light-scattering detection technique for phosphatidylethanol quantitation. This method had a total coefficient of variation of <20% at the detection limit of 0.2 nmol, equaling 0.8 micromol/liter of whole blood. Two groups were studied. (a) Five healthy volunteers were given 32 to 47 g of ethanol in a single dose, to give blood ethanol levels of approximately 25 mmol/liter after 30 to 60 min. Phosphatidylethanol, carbohydrate-deficient transferrin (CDT), and blood ethanol were measured before and after the intake. (b) Twelve student volunteers were studied during a 3 week period of prolonged alcohol consumption (total estimated intake: 1334 +/- 488 g, mean +/- SD) and phosphatidylethanol, serum-CDT, gamma-glutamyltransferase, and blood ethanol were measured at the start of the period (day 1) and twice at the end of the period (days 18 and 21). In group (a), no phosphatidylethanol was detected at any time after ethanol dosage/intake. In group (b), no blood phosphatidylethanol or blood ethanol could be demonstrated at the start, and serum-CDT was below the discrimination limit (1.3%) in all persons. No phosphatidylethanol was detected in those four persons with the lowest intake (742 +/- 150 g). However, the remaining eight persons had detectable levels of phosphatidylethanol (1.0 to 2.1 micromol/liter), and these had a higher total intake (1630 +/- 389 g). There was a statistically significant (p = 0.02) increase in serum CDT for 3 weeks. However, only 3 of 12 persons increased above the discrimination limit. The present results indicate that a substantial alcohol intake is needed to elevate blood phosphatidylethanol. In comparison with serum-CDT, blood phosphatidylethanol appears more sensitive.

摘要

磷脂酰乙醇是一种“病理性”磷脂,仅在乙醇存在的情况下通过磷脂酶D的作用形成。本研究旨在阐明与其他滥用标志物相比,不同水平和模式的酒精摄入如何影响血液中磷脂酰乙醇的水平。我们使用了一种新的高效液相色谱-蒸发光散射检测技术来定量磷脂酰乙醇。该方法在0.2纳摩尔的检测限下总变异系数<20%,相当于全血0.8微摩尔/升。研究了两组。(a) 五名健康志愿者单次服用32至47克乙醇,30至60分钟后血液乙醇水平约为25毫摩尔/升。在摄入前后测量磷脂酰乙醇、缺糖转铁蛋白(CDT)和血液乙醇。(b) 十二名学生志愿者在为期3周的长期饮酒期间接受研究(估计总摄入量:1334±488克,平均值±标准差),并在该期间开始时(第1天)以及结束时(第18天和第21天)测量两次磷脂酰乙醇、血清CDT、γ-谷氨酰转移酶和血液乙醇。在(a)组中,乙醇给药/摄入后的任何时间都未检测到磷脂酰乙醇。在(b)组中,开始时未检测到血液磷脂酰乙醇或血液乙醇,并且所有人员的血清CDT均低于鉴别限(1.3%)。摄入最少(742±150克)的四名人员中未检测到磷脂酰乙醇。然而,其余八名人员的磷脂酰乙醇水平可检测到(1.0至2.1微摩尔/升),且这些人员的总摄入量较高(1630±389克)。血清CDT在3周内有统计学显著升高(p = 0.02)。然而,12名人员中只有3人升高超过鉴别限。目前的结果表明,需要大量饮酒才能提高血液中磷脂酰乙醇的水平。与血清CDT相比,血液磷脂酰乙醇似乎更敏感。

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