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Published on: June 23, 2023
Reference values for the alcohol biomarker phosphatidylethanol (PEth) in the Belgian population: Insights from a
Kevin Vandenbroucke1, Katleen Van Uytfanghe1, Liesl Heughebaert1
1Laboratory of Toxicology, Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.
Background:
Phosphatidylethanol 16:0/18:1 (PEth) is a well-established direct biomarker for monitoring recent and chronic alcohol consumption. However, population-based surveys assessing PEth in both people who drink alcohol and people who do not drink alcohol remain limited, despite their value for contextualizing forensic and clinical results.
Methods:
PEth was quantified in samples collected during the 2022-2023 Belgian National Food Consumption Survey (n = 487) using capillary volumetric absorptive microsampling (VAMS) and an ISO17025-accredited liquid chromatography-tandem mass spectrometry method (10-2000 ng/mL). Participants also completed an AUDIT-C questionnaire; relationships with PEth were evaluated using Spearman correlation and Cohen's kappa. Weighted data were used to derive estimates for the general Belgian population and compared with two presumed higher-consumption subgroups.
Results:
PEth concentrations in the general Belgian population ranged from <10 to 1400 ng/mL. Overall, 35.7% had concentrations between 20 and 200 ng/mL and 10.7% exceeded 200 ng/mL. PEth correlated strongly with AUDIT-C scores, with Spearman's rank correlation coefficients of 0.61 in males and 0.64 in females. Agreement between PEth and AUDIT-C for identifying hazardous drinking was moderate in males and substantial in females (Cohen's kappa: 0.55 and 0.63, respectively). The median PEth concentration in the general population was 17 ng/mL (95% CI: 15-18), compared with 32 ng/mL in a non-abstinent adult population and 122 ng/mL in individuals enrolled in a driver's license regranting program.
Conclusion:
These findings provide population-based PEth reference data for Belgium and demonstrate clear differences in PEth distributions between general and higher-exposure populations, supporting improved contextual interpretation of forensic and clinical PEth results.

