Abstract
Alcohol use can potentiate liver diseases such as hepatitis C and in sufficient quantities can itself cause significant liver disease over time. This chapter will briefly review the importance of alcohol use in liver diseases and difficulties that can arise when clinicians attempt to gather an accurate drinking history in patients with liver disease. The bulk of the chapter focuses on the use of blood phosphatidylethanol (PEth) as an alcohol consumption biomarker in liver disease patients, including validation in this population, potential uses in clinical care and research, and current limitations to its use for these purposes.
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Abbreviations
- %dCDT:
-
% disialo-carbohydrate-deficient transferrin
- ALT:
-
Alanine transaminase
- AST:
-
Aspartate aminotransferase
- CDT:
-
Carbohydrate-deficient transferrin
- ELSD:
-
Evaporative light scattering detection
- EtG:
-
Ethyl glucuronide
- GGT:
-
Gamma-glutamyltransferase
- HPLC:
-
High-performance liquid chromatography
- MCV:
-
Mean corpuscular volume
- MS:
-
Mass spectrometry
- MS/MS:
-
Tandem mass spectrometry
- PEth:
-
Phosphatidylethanol
- ROC:
-
Receiver operating characteristic
References
Alling C, Gustavsson L, Anggard E. An abnormal phospholipid in rat organs after ethanol treatment. FEBS Lett. 1983;152:24–8.
Aradottir S, Asanovska G, Gjerss S, et al. Phosphatidylethanol (PEth) concentrations in blood are correlated to reported alcohol intake in alcohol-dependent patients. Alcohol Alcohol. 2006;41:431–7.
Arndt T, van der Meijden BB, Wielders JP. Atypical serum transferrin isoform distribution in liver cirrhosis studied by HPLC, capillary electrophoresis and transferrin genotyping. Clin Chim Acta. 2008;394:42–6.
Babor TF, de la Fuente JR, Saunders J, Grant M. AUDIT. The alcohol use disorders identification test. Guidelines for use in primary health care. Geneva: World Health Organization; 1992.
Barve A, Khan R, Marsano L, et al. Treatment of alcoholic liver disease. Ann Hepatol. 2008;7:5–15.
Bergstrom JP, Helander A. Clinical characteristics of carbohydrate-deficient transferrin (%disialotransferrin) measured by HPLC: sensitivity, specificity, gender effects, and relationship with other alcohol biomarkers. Alcohol Alcohol. 2008;43:436–41.
Bradley KA, Debenedetti AF, Volk RJ, et al. AUDIT-C as a brief screen for alcohol misuse in primary care. Alcohol Clin Exp Res. 2007;31:1208–17.
Cohen JI, Nagy LE. Pathogenesis of alcoholic liver disease: interactions between parenchymal and non-parenchymal cells. J Dig Dis. 2011;12:3–9.
Conigrave KM, Davies P, Haber P, Whitfield JB. Traditional markers of excessive alcohol use. Addiction. 2003;98 Suppl 2:31–43.
Society of Hair Testing, Consensus for the use of alcohol markers in hair for assessment of both abstinence and chronic excessive alcohol consumption. Bordeaux. 2014.
Del Boca FK, Darkes J. The validity of self-reports of alcohol consumption: state of the science and challenges for research. Addiction. 2003;98 Suppl 2:1–12.
Dimartini A, Day N, Lane T, et al. Carbohydrate deficient transferrin in abstaining patients with end-stage liver disease. Alcohol Clin Exp Res. 2001;25:1729–33.
Dresen S, Weinmann W, Wurst FM. Forensic confirmatory analysis of ethyl sulfate – a new marker for alcohol consumption – by liquid-chromatography/electrospray ionization/tandem mass spectrometry. J Am Soc Mass Spectrom. 2004;15:1644–8.
Erim Y, Bottcher M, Dahmen U, et al. Urinary ethyl glucuronide testing detects alcohol consumption in alcoholic liver disease patients awaiting liver transplantation. Liver Transpl. 2007;13:757–61.
Gnann H, Engelmann C, Skopp G, et al. Identification of 48 homologues of phosphatidylethanol in blood by LC-ESI-MS/MS. Anal Bioanal Chem. 2010;396:2415–23.
Gnann H, Weinmann W, Thierauf A. Formation of phosphatidylethanol and its subsequent elimination during an extensive drinking experiment over 5 days. Alcohol Clin Exp Res. 2012;36:1507–11.
Gunnarsson T, Karlsson A, Hansson P, et al. Determination of phosphatidylethanol in blood from alcoholic males using high-performance liquid chromatography and evaporative light scattering or electrospray mass spectrometric detection. J Chromatogr B Biomed Sci Appl. 1998;705:243–9.
Gustavsson L. Phosphatidylethanol formation: specific effects of ethanol mediated via phospholipase D. Alcohol Alcohol. 1995;30:391–406.
Hahn JA, Dobkin LM, Mayanja B, et al. Phosphatidylethanol (PEth) as a biomarker of alcohol consumption in HIV-positive patients in sub-Saharan Africa. Alcohol Clin Exp Res. 2012;36:854–62.
Hansson P, Caron M, Johnson G, et al. Blood phosphatidylethanol as a marker of alcohol abuse: levels in alcoholic males during withdrawal. Alcohol Clin Exp Res. 1997;21:108–10.
Hartmann S, Aradottir S, Graf M, et al. Phosphatidylethanol as a sensitive and specific biomarker: comparison with gamma-glutamyl transpeptidase, mean corpuscular volume and carbohydrate-deficient transferrin. Addict Biol. 2007;12:81–4.
Holbrook PG, Pannell LK, Murata Y, Daly JW. Molecular species analysis of a product of phospholipase D activation. Phosphatidylethanol is formed from phosphatidylcholine in phorbol ester- and bradykinin-stimulated PC12 cells. J Biol Chem. 1992;267:16834–40.
Jain J, Evans JL, Briceno A, et al. Comparison of phosphatidylethanol results to self-reported alcohol consumption among young injection drug users. Alcohol Alcohol. 2014;49:520–4.
Kim WR, Lake JR, Smith JM, et al. OPTN/SRTR 2013 annual data report: liver. Am J Transplant. 2015;15 Suppl 2:1–28.
Kwak HS, Han JY, Ahn HK, et al. Blood levels of phosphatidylethanol in pregnant women reporting positive alcohol ingestion, measured by an improved LC-MS/MS analytical method. Clin Toxicol. 2012;50:886–91.
Morini L, Politi L, Groppi A, et al. Determination of ethyl glucuronide in hair samples by liquid chromatography/electrospray tandem mass spectrometry. J Mass Spectrom. 2006;41:34–42.
Mueller GC, Fleming MF, Lemahieu MA, et al. Synthesis of phosphatidylethanol – a potential marker for adult males at risk for alcoholism. Proc Natl Acad Sci U S A. 1988;85:9778–82.
Nissinen AE, Makela SM, Vuoristo JT, et al. Immunological detection of in vitro formed phosphatidylethanol – an alcohol biomarker – with monoclonal antibodies. Alcohol Clin Exp Res. 2008;32:921–8.
Pragst F, Rothe M, Moench B, et al. Combined use of fatty acid ethyl esters and ethyl glucuronide in hair for diagnosis of alcohol abuse: interpretation and advantages. Forensic Sci Int. 2010;196:101–10.
Sobell L, Sobell M. Timeline follow-back: a technique for assessing self-reported ethanol consumption. In: Litten RZ, Allen JP, editors. Measuring alcohol consumption: psychosocial and biological methods. Totowa: Humana Press; 1992. p. 41–72.
Staufer K, Andresen H, Vettorazzi E, et al. Urinary ethyl glucuronide as a novel screening tool in patients pre- and post-liver transplantation improves detection of alcohol consumption. Hepatology. 2011;54:1640–9.
Stewart SH, Reuben A, Brzezinski WA, et al. Preliminary evaluation of phosphatidylethanol and alcohol consumption in patients with liver disease and hypertension. Alcohol Alcohol. 2009;44:464–7.
Stewart SH, Law TL, Randall PK, Newman R. Phosphatidylethanol and alcohol consumption in reproductive age women. Alcohol Clin Exp Res. 2010;34:488–92.
Stewart SH, Koch DG, Burgess DM, et al. Sensitivity and specificity of urinary ethyl glucuronide and ethyl sulfate in liver disease patients. Alcohol Clin Exp Res. 2013a;37:150–5.
Stewart SH, Koch DG, Willner IR, et al. Hair ethyl glucuronide is highly sensitive and specific for detecting moderate-to-heavy drinking in patients with liver disease. Alcohol Alcohol. 2013b;48:83–7.
Stewart SH, Koch DG, Willner IR, et al. Validation of blood phosphatidylethanol as an alcohol consumption biomarker in patients with chronic liver disease. Alcohol Clin Exp Res. 2014;38:1706–11.
Szabo G, Wands JR, Eken A, et al. Alcohol and hepatitis C virus – interactions in immune dysfunctions and liver damage. Alcohol Clin Exp Res. 2010;34:1675–86.
UKPDS Writing Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. Lancet. 1998;352:837–53.
Varga A, Alling C. Formation of phosphatidylethanol in vitro in red blood cells from healthy volunteers and chronic alcoholics. J Lab Clin Med. 2002;140:79–83.
Varga A, Hansson P, Johnson G, Alling C. Normalization rate and cellular localization of phosphatidylethanol in whole blood from chronic alcoholics. Clin Chim Acta. 2000;299:141–50.
Wrighton SA, Pai JK, Mueller GC. Demonstration of two unique metabolites of arachidonic acid from phorbol ester-stimulated bovine lymphocytes. Carcinogenesis. 1983;4:1247–51.
Wurst FM, Seidl S, Ladewig D, et al. Ethyl glucuronide: on the time course of excretion in urine during detoxification. Addict Biol. 2002;7:427–34.
Wurst FM, Alexson S, Wolfersdorf M, et al. Concentration of fatty acid ethyl esters in hair of alcoholics: comparison to other biological state markers and self reported-ethanol intake. Alcohol Alcohol. 2004a;39:33–8.
Wurst FM, Wiesbeck GA, Metzger JW, Weinmann W. On sensitivity, specificity, and the influence of various parameters on ethyl glucuronide levels in urine – results from the WHO/ISBRA study. Alcohol Clin Exp Res. 2004b;28:1220–8.
Wurst FM, Thon N, Aradottir S, et al. Phosphatidylethanol: normalization during detoxification, gender aspects and correlation with other biomarkers and self-reports. Addict Biol. 2010;15:88–95.
Yoon Y, Yi H. Surveillance report # 88- liver cirrhosis mortality in the United States, 1970–2007. US Department of Health and Human Services, Public Health Service, National Institutes of Health; 2010.
Zakhari S, Li TK. Determinants of alcohol use and abuse: impact of quantity and frequency patterns on liver disease. Hepatology. 2007;46:2032–9.
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Stewart, S.H. (2017). Phosphatidylethanol and Alcohol Use in Liver Disease Patients. In: Patel, V., Preedy, V. (eds) Biomarkers in Liver Disease. Biomarkers in Disease: Methods, Discoveries and Applications. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-7675-3_18
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DOI: https://doi.org/10.1007/978-94-007-7675-3_18
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