Back to Search Start Over

Phosphatidylethanol in patients with liver diseases of different etiologies: Analysis of six homologues and comparison with other alcohol markers

Authors :
Alexander Müller
Amadea Mosebach
Stefanie Iwersen-Bergmann
Martina Sterneck
Hilke Jungen
Anne Szewczyk
Maria Rodriguez Lago
Nadine Aboutara
Eik Vettorazzi
Source :
Clinica chimica acta; international journal of clinical chemistry. 524
Publication Year :
2021

Abstract

Background and aims Phosphatidylethanol (PEth) is a direct alcohol biomarker. Aim of the study was to evaluate the performance of six homologues of PEth in comparison to other alcohol markers in patients with liver diseases. Methods The study included 234 patients with liver disease, who gave statements about alcohol consumption during the three months prior to the doctor’s appointment. Ethylglucuronide in urine (uEtG) and in hair (hEtG) and carbohydrate deficient transferrin (CDT) were analyzed in addition to PEth. Results Of all patients 47 % stated to have drunk alcohol during the past three months. UEtG, hEtG and CDT showed a sensitivity of 29% and a specificity of 92% together for ingestion of at least two standard drinks (24g) per week. With PEth 16:0/18:1 in addition, sensitivity increased to 59%. For consumption in the last week uEtG’s sensitivity and specificity was 28% and 100%, respectively. PEth’s was 75% and 93%. When looking at patients who consumed at least two standard drinks during the past three months and of which a hair sample could be obtained, hEtG’s sensitivity was 37% and specificity 90%. PEth had a sensitivity of 53% and specificity of 100%. Quotients of PEth 16:0/18:1 with 16:0/18:2, 16:0/20:4 and 18:0/18:2 were smaller when alcohol had been consumed more recently. Conclusion Despite the rather poor overall sensitivity of alcohol biomarkers in this study, PEth showed best sensitivity for all time periods of alcohol consumption.

Details

ISSN :
18733492
Volume :
524
Database :
OpenAIRE
Journal :
Clinica chimica acta; international journal of clinical chemistry
Accession number :
edsair.doi.dedup.....51686aab376f7767381cd1764a47c6e9