Literature DB >> 9835304

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

A Varga1, P Hansson, C Lundqvist, C Alling.   

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.

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Year:  1998        PMID: 9835304

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  22 in total

1.  Validation of blood phosphatidylethanol as an alcohol consumption biomarker in patients with chronic liver disease.

Authors:  Scott H Stewart; David G Koch; Ira R Willner; Raymond F Anton; Adrian Reuben
Journal:  Alcohol Clin Exp Res       Date:  2014-05-21       Impact factor: 3.455

Review 2.  Biomarkers for detection of alcohol consumption in liver transplantation.

Authors:  Katharina Staufer; Michel Yegles
Journal:  World J Gastroenterol       Date:  2016-04-14       Impact factor: 5.742

3.  Comparison of direct and indirect alcohol markers with PEth in blood and urine in alcohol dependent inpatients during detoxication.

Authors:  M Winkler; G Skopp; A Alt; E Miltner; Th Jochum; C Daenhardt; F Sporkert; H Gnann; W Weinmann; A Thierauf
Journal:  Int J Legal Med       Date:  2012-12-29       Impact factor: 2.686

4.  Phosphatidylethanol (PEth) as a biomarker of alcohol consumption in HIV-positive patients in sub-Saharan Africa.

Authors:  Judith A Hahn; Loren M Dobkin; Bernard Mayanja; Nneka I Emenyonu; Isaac M Kigozi; Stephen Shiboski; David R Bangsberg; Heike Gnann; Wolfgang Weinmann; Friedrich M Wurst
Journal:  Alcohol Clin Exp Res       Date:  2011-12-07       Impact factor: 3.455

5.  Differences in the Synthesis and Elimination of Phosphatidylethanol 16:0/18:1 and 16:0/18:2 After Acute Doses of Alcohol.

Authors:  Nathalie Hill-Kapturczak; Donald M Dougherty; John D Roache; Tara E Karns-Wright; Martin A Javors
Journal:  Alcohol Clin Exp Res       Date:  2018-03-30       Impact factor: 3.455

6.  Detection of phosphatidylethanol (PEth) in the blood of drivers in an alcohol ignition interlock program.

Authors:  Paul Marques; Therese Hansson; Anders Isaksson; Lisa Walther; Joseph Jones; Douglas Lewis; Mary Jones
Journal:  Traffic Inj Prev       Date:  2011-04       Impact factor: 1.491

Review 7.  [What ethanol metabolites as biological markers tell us about alcohol use].

Authors:  Friedrich Martin Wurst; Natasha Thon; Wolfgang Weinmann; Michel Yegles; Ulrich Preuss
Journal:  Wien Med Wochenschr       Date:  2013-12-10

8.  Estimating driver risk using alcohol biomarkers, interlock blood alcohol concentration tests and psychometric assessments: initial descriptives.

Authors:  Paul Marques; Scott Tippetts; John Allen; Martin Javors; Christer Alling; Michel Yegles; Fritz Pragst; Friedrich Wurst
Journal:  Addiction       Date:  2009-11-16       Impact factor: 6.526

9.  Associations Between the Phosphatidylethanol Alcohol Biomarker and Self-Reported Alcohol Use in a Sample of HIV-Infected Outpatient Drinkers in Western Kenya.

Authors:  Rebecca K Papas; Benson N Gakinya; Michael M Mwaniki; Alfred K Keter; Hana Lee; Michelle P Loxley; Debra A Klein; John E Sidle; Steve Martino; Joyce B Baliddawa; Kathryn L Schlaudt; Stephen A Maisto
Journal:  Alcohol Clin Exp Res       Date:  2016-07-18       Impact factor: 3.455

10.  Measurement of direct ethanol metabolites in a case of a former driving under the influence (DUI) of alcohol offender, now claiming abstinence.

Authors:  Friedrich M Wurst; Michel Yegles; Christer Alling; Steina Aradottir; Jutta Dierkes; Gerhard A Wiesbeck; Claudia C Halter; Fritz Pragst; Volker Auwaerter
Journal:  Int J Legal Med       Date:  2008-02-06       Impact factor: 2.686

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