Biomarkers for monitoring alcohol sobriety after liver transplantation for alcoholic liver disease.


Journal

Journal of gastroenterology and hepatology
ISSN: 1440-1746
Titre abrégé: J Gastroenterol Hepatol
Pays: Australia
ID NLM: 8607909

Informations de publication

Date de publication:
Aug 2023
Historique:
revised: 08 06 2023
received: 31 05 2023
accepted: 08 06 2023
medline: 31 8 2023
pubmed: 24 6 2023
entrez: 24 6 2023
Statut: ppublish

Résumé

Alcoholic liver disease (ALD) has become the most common indication for liver transplantation in Western countries, and its incidence is rapidly increasing in East Asia. Alcohol abstinence remains the standard of care for promoting liver transplantation for ALD and for preventing posttransplant graft loss. However, efficient monitoring methods are still being developed due to the limitations of traditional biomarkers, interviews, and questionnaires. The development of alcohol biomarkers has shifted from detecting alcohol and methanol to indirect byproducts, and to current mid-term and long-term direct alcohol metabolites, which provide higher accuracy and cover almost all types of alcohol relapse detection. However, in most clinical studies, biomarkers are used and validated in healthy individuals and alcohol use disorder (AUD) patients and for pretransplant evaluations. The evidence for their use in posttransplant abstinence monitoring is still lacking, but it is crucial for early detection of alcohol relapse and initiating intervention. This review aims to summarize the current evidence of the use of biomarkers for monitoring sobriety and alcohol relapse after liver transplantation, as well as to cover the diagnostic accuracy, detection window, and optimal multidisciplinary strategies.

Identifiants

pubmed: 37353915
doi: 10.1111/jgh.16269
doi:

Substances chimiques

Ethanol 3K9958V90M
Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1227-1232

Subventions

Organisme : Research Grants Council, University Grants Committee
ID : 17106921
Organisme : Research Grants Council, University Grants Committee
ID : 17124219
Organisme : Research Grants Council, University Grants Committee
ID : C7021-21G
Organisme : Research Grants Council, University Grants Committee
ID : T12-703/19-R

Informations de copyright

© 2023 The Authors. Journal of Gastroenterology and Hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

Références

Cholankeril G, Ahmed A. Alcoholic liver disease replaces hepatitis C virus infection as the leading indication for liver transplantation in the United States. Clin. Gastroenterol. Hepatol. 2018; 16: 1356-1358.
Xiao J, Wang F, Wong NK et al. Epidemiological realities of alcoholic liver disease: global burden, research trends, and therapeutic promise. Gene Expr. 2020; 20: 105-118.
Huang DQ, Mathurin P, Cortez-Pinto H, Loomba R. Global epidemiology of alcohol-associated cirrhosis and HCC: trends, projections and risk factors. Nat. Rev. Gastroenterol. Hepatol. 2023; 20: 37-49.
Niu X, Zhu L, Xu Y et al. Global prevalence, incidence, and outcomes of alcohol related liver diseases: a systematic review and meta-analysis. BMC Public Health 2023; 23: 859.
Im GY, Kim-Schluger L, Shenoy A et al. Early liver transplantation for severe alcoholic hepatitis in the United States--a single-center experience. Am. J. Transplant. 2016; 16: 841-849.
Mathurin P, Moreno C, Samuel D et al. Early liver transplantation for severe alcoholic hepatitis. N. Engl. J. Med. 2011; 365: 1790-1800.
Antonini TM, Guillaud O, Dumortier J et al. Impact of a first study of early transplantation in acute alcoholic hepatitis: results of a nationwide survey in French liver transplantation programs. Liver Transpl. 2018; 24: 841-844.
Bittermann T, Mahmud N, Weinberg EM, Reddy KR. Rising trend in waitlisting for alcoholic hepatitis with more favorable outcomes than other high model for end-stage liver disease in the current era. Transplantation 2022; 106: 1401-1410.
Lim N, Kwong AJ, Jafri SM et al. Heterogeneity in center practices in liver transplantation for alcohol-associated liver disease in the United States. Am. J. Gastroenterol. 2022; 117: 1530-1535.
Burra P, Senzolo M, Adam R et al. Liver transplantation for alcoholic liver disease in Europe: a study from the ELTR (European Liver Transplant Registry). Am. J. Transplant. 2010; 10: 138-148.
Kodali S, Kaif M, Tariq R, Singal AK. Alcohol relapse after liver transplantation for alcoholic cirrhosis-impact on liver graft and patient survival: a meta-analysis. Alcohol Alcohol. 2018; 53: 166-172.
Pfitzmann R, Schwenzer J, Rayes N, Seehofer D, Neuhaus R, Nussler NC. Long-term survival and predictors of relapse after orthotopic liver transplantation for alcoholic liver disease. Liver Transpl. 2007; 13: 197-205.
Dumortier J, Dharancy S, Cannesson A et al. Recurrent alcoholic cirrhosis in severe alcoholic relapse after liver transplantation: a frequent and serious complication. Am. J. Gastroenterol. 2015; 110: 1160-1166.
Cuadrado A, Fabrega E, Casafont F, Pons-Romero F. Alcohol recidivism impairs long-term patient survival after orthotopic liver transplantation for alcoholic liver disease. Liver Transpl. 2005; 11: 420-426.
Mackie J, Groves K, Hoyle A et al. Orthotopic liver transplantation for alcoholic liver disease: a retrospective analysis of survival, recidivism, and risk factors predisposing to recidivism. Liver Transpl. 2001; 7: 418-427.
Chuncharunee L, Yamashiki N, Thakkinstian A, Sobhonslidsuk A. Alcohol relapse and its predictors after liver transplantation for alcoholic liver disease: a systematic review and meta-analysis. BMC Gastroenterol. 2019; 19: 150.
Masson S, Aldersley H, Leithead JA et al. Liver transplantation for alcohol-related liver disease in the UK: revised UK Liver Advisory Group recommendations for referral. Lancet Gastroenterol. Hepatol. 2021; 6: 947-955.
European Association for the Study of the Liver. EASL clinical practice guidelines: management of alcohol-related liver disease. J. Hepatol. 2018; 69: 154-181.
Crabb DW, Im GY, Szabo G, Mellinger JL, Lucey MR. Diagnosis and treatment of alcohol-associated liver diseases: 2019 practice guidance from the American Association for the Study of Liver Diseases. Hepatology 2020; 71: 306-333.
Asrani SK, Trotter J, Lake J et al. Meeting report: the Dallas consensus conference on liver transplantation for alcohol associated hepatitis. Liver Transpl. 2020; 26: 127-140.
Gough G, Heathers L, Puckett D et al. The utility of commonly used laboratory tests to screen for excessive alcohol use in clinical practice. Alcohol. Clin. Exp. Res. 2015; 39: 1493-1500.
Staufer K, Yegles M. Biomarkers for detection of alcohol consumption in liver transplantation. World J. Gastroenterol. 2016; 22: 3725-3734.
Arnts J, Vanlerberghe BTK, Roozen S et al. Diagnostic accuracy of biomarkers of alcohol use in patients with liver disease: a systematic review. Alcohol. Clin. Exp. Res. 2021; 45: 25-37.
Heier C, Xie H, Zimmermann R. Nonoxidative ethanol metabolism in humans-from biomarkers to bioactive lipids. IUBMB Life 2016; 68: 916-923.
Cappelle D, Neels H, De Keukeleire S et al. Ethyl glucuronide in keratinous matrices as biomarker of alcohol use: a correlation study between hair and nails. Forensic Sci. Int. 2017; 279: 187-191.
Fosen JT, Morini L, Sempio C et al. Ethyl glucuronide elimination kinetics in fingernails and comparison to levels in hair. Alcohol Alcohol. 2017; 52: 580-586.
Helander A, Zheng Y. Molecular species of the alcohol biomarker phosphatidylethanol in human blood measured by LC-MS. Clin. Chem. 2009; 55: 1395-1405.
Schrock A, Thierauf-Emberger A, Schurch S, Weinmann W. Phosphatidylethanol (PEth) detected in blood for 3 to 12 days after single consumption of alcohol-a drinking study with 16 volunteers. Int. J. Leg. Med. 2017; 131: 153-160.
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: 1507-1511.
Stewart SH, Koch DG, Willner IR, Anton RF, Reuben A. Validation of blood phosphatidylethanol as an alcohol consumption biomarker in patients with chronic liver disease. Alcohol. Clin. Exp. Res. 2014; 38: 1706-1711.
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: 141-150.
Arndt T. Carbohydrate-deficient transferrin as a marker of chronic alcohol abuse: a critical review of preanalysis, analysis, and interpretation. Clin. Chem. 2001; 47: 13-27.
Andresen-Streichert H, Beres Y, Weinmann W et al. Improved detection of alcohol consumption using the novel marker phosphatidylethanol in the transplant setting: results of a prospective study. Transpl. Int. 2017; 30: 611-620.
Staufer K, Andresen H, Vettorazzi E, Tobias N, Nashan B, Sterneck M. Urinary ethyl glucuronide as a novel screening tool in patients pre- and post-liver transplantation improves detection of alcohol consumption. Hepatology 2011; 54: 1640-1649.
Piano S, Marchioro L, Gola E et al. Assessment of alcohol consumption in liver transplant candidates and recipients: the best combination of the tools available. Liver Transpl. 2014; 20: 815-822.
Fleming MF, Smith MJ, Oslakovic E et al. Phosphatidylethanol Detects Moderate-to-Heavy Alcohol Use in Liver Transplant Recipients. Alcohol. Clin. Exp. Res. 2017; 41: 857-862.
Stewart SH, Reuben A, Anton RF. Relationship of abnormal chromatographic pattern for carbohydrate-deficient transferrin with severe liver disease. Alcohol Alcohol. 2017; 52: 24-28.
Berlakovich GA, Soliman T, Freundorfer E et al. Pretransplant screening of sobriety with carbohydrate-deficient transferrin in patients suffering from alcoholic cirrhosis. Transpl. Int. 2004; 17: 617-621.
Kenan N, Larsson A, Axelsson O, Helander A. Changes in transferrin glycosylation during pregnancy may lead to false-positive carbohydrate-deficient transferrin (CDT) results in testing for riskful alcohol consumption. Clin. Chim. Acta 2011; 412: 129-133.
Hempel JM, Greif-Higer G, Kaufmann T, Beutel ME. Detection of alcohol consumption in patients with alcoholic liver cirrhosis during the evaluation process for liver transplantation. Liver Transpl. 2012; 18: 1310-1315.
Andresen-Streichert H, von Rothkirch G, Vettorazzi E et al. Determination of ethyl glucuronide in hair for detection of alcohol consumption in patients after liver transplantation. Ther. Drug Monit. 2015; 37: 539-545.
Hoiseth G, Morini L, Ganss R, Nordal K, Morland J. Higher levels of hair ethyl glucuronide in patients with decreased kidney function. Alcohol. Clin. Exp. Res. 2013; 37: E14-E16.
Pirro V, Di Corcia D, Seganti F, Salomone A, Vincenti M. Determination of ethyl glucuronide levels in hair for the assessment of alcohol abstinence. Forensic Sci. Int. 2013; 232: 229-236.
Arndt T, Schrofel S, Stemmerich K. Ethyl glucuronide identified in commercial hair tonics. Forensic Sci. Int. 2013; 231: 195-198.
Suesse S, Pragst F, Mieczkowski T et al. Practical experiences in application of hair fatty acid ethyl esters and ethyl glucuronide for detection of chronic alcohol abuse in forensic cases. Forensic Sci. Int. 2012; 218: 82-91.
Ettlinger J, Kirchen L, Yegles M. Influence of thermal hair straightening on ethyl glucuronide content in hair. Drug Test. Anal. 2014; 6: 74-77.
DiMartini A, Day N, Dew MA et al. Alcohol consumption patterns and predictors of use following liver transplantation for alcoholic liver disease. Liver Transpl. 2006; 12: 813-820.
DiMartini A, Dew MA, Day N et al. Trajectories of alcohol consumption following liver transplantation. Am. J. Transplant. 2010; 10: 2305-2312.
DiMartini AF, Leggio L, Singal AK. Barriers to the management of alcohol use disorder and alcohol-associated liver disease: strategies to implement integrated care models. Lancet Gastroenterol. Hepatol. 2022; 7: 186-195.
Arab JP, Bataller R. Advancing alcohol-related liver disease: from novel biomarkers to refining selection for liver transplantation. Nat. Rev. Gastroenterol. Hepatol. 2023; 20: 71-72.
Maas SCE, Vidaki A, Teumer A et al. Validating biomarkers and models for epigenetic inference of alcohol consumption from blood. Clin. Epigenetics 2021; 13: 198.

Auteurs

Jiang Liu (J)

Department of Surgery, LKS Faculty of Medicine and HKU-Shenzhen Hospital, The University of Hong Kong, Hong Kong, Hong Kong.
Hepato-pancreato-biliary Center, Beijing Tsinghua Changgung Hospital, Tsinghua University, Beijing, China.

Kwan Man (K)

Department of Surgery, LKS Faculty of Medicine and HKU-Shenzhen Hospital, The University of Hong Kong, Hong Kong, Hong Kong.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH