Positive blood phosphatidylethanol concentration is associated with unfavorable waitlist-related outcomes for patients medically appropriate for liver transplantation.

alcohol biomarker alcohol use disorder alcohol-associated liver disease liver transplantation phosphatidylethanol

Journal

Alcoholism, clinical and experimental research
ISSN: 1530-0277
Titre abrégé: Alcohol Clin Exp Res
Pays: England
ID NLM: 7707242

Informations de publication

Date de publication:
04 2022
Historique:
revised: 23 01 2022
received: 10 09 2021
accepted: 25 01 2022
pubmed: 2 2 2022
medline: 20 4 2022
entrez: 1 2 2022
Statut: ppublish

Résumé

Excessive alcohol use is a leading etiology of liver disease and indication for liver transplantation. Accurate measurement of alcohol use remains a challenge in the management of patients in the pre-, peri-, and post-liver transplant settings. Blood 16:0-18:1 phosphatidylethanol (PEth) concentration is a sensitive and specific biomarker of binge and moderate, chronic alcohol use. As PEth has the longest detection window of available blood-based direct alcohol biomarkers for moderate to heavy drinking, it shows promise as an indicator of patterns and chronicity of drinking. However, the utility of PEth in clinical liver transplantation is understudied. This study examines the association of PEth results with liver transplantation waitlist-focused patient outcomes. Retrospective data for all patients tested for PEth for a one-year period at a tertiary care medical center with an active liver transplantation program were abstracted. Indications for PEth testing, liver transplantation waitlist-related outcomes (e.g., listing and delisting) following testing and associations of PEth results with other parameters were analyzed. Over a one-year period, 153 PEth tests were performed on 109 individuals. The most frequent indications for PEth testing were as an objective indicator of alcohol use patterns (86.3%) and to assess alcohol as a putative etiology of liver injury (13.7%). Of the 109 patients, 56 were medically appropriate for liver transplantation. Medically acceptable candidates with unfavorable transplantation waitlist-related outcomes (delisting, deferment of transplant evaluation, deferment of listing until completion of recommended alcohol rehabilitation, and being deemed not a transplant candidate) were at least 3.41 times more likely to have a positive PEth test than those with favorable transplantation waitlist-related outcomes (odds ratio 3.41, confidence interval 3.41 to ∞, p = 0.001). This single-center study reporting a comprehensive account of PEth utilization at a liver transplant center demonstrates that liver transplantation waitlist-related outcomes are associated with PEth test results. Patients with positive PEth tests were more likely to have unfavorable transplant waitlist-related outcomes. PEth testing has not been validated as a predictor of relapse to drinking in post-transplant patients and because its utility in the pre-transplant setting is unclear its use could lead to disparities in the selection of patients for liver transplantation.

Sections du résumé

BACKGROUND
Excessive alcohol use is a leading etiology of liver disease and indication for liver transplantation. Accurate measurement of alcohol use remains a challenge in the management of patients in the pre-, peri-, and post-liver transplant settings. Blood 16:0-18:1 phosphatidylethanol (PEth) concentration is a sensitive and specific biomarker of binge and moderate, chronic alcohol use. As PEth has the longest detection window of available blood-based direct alcohol biomarkers for moderate to heavy drinking, it shows promise as an indicator of patterns and chronicity of drinking. However, the utility of PEth in clinical liver transplantation is understudied. This study examines the association of PEth results with liver transplantation waitlist-focused patient outcomes.
METHODS
Retrospective data for all patients tested for PEth for a one-year period at a tertiary care medical center with an active liver transplantation program were abstracted. Indications for PEth testing, liver transplantation waitlist-related outcomes (e.g., listing and delisting) following testing and associations of PEth results with other parameters were analyzed.
RESULTS
Over a one-year period, 153 PEth tests were performed on 109 individuals. The most frequent indications for PEth testing were as an objective indicator of alcohol use patterns (86.3%) and to assess alcohol as a putative etiology of liver injury (13.7%). Of the 109 patients, 56 were medically appropriate for liver transplantation. Medically acceptable candidates with unfavorable transplantation waitlist-related outcomes (delisting, deferment of transplant evaluation, deferment of listing until completion of recommended alcohol rehabilitation, and being deemed not a transplant candidate) were at least 3.41 times more likely to have a positive PEth test than those with favorable transplantation waitlist-related outcomes (odds ratio 3.41, confidence interval 3.41 to ∞, p = 0.001).
CONCLUSION
This single-center study reporting a comprehensive account of PEth utilization at a liver transplant center demonstrates that liver transplantation waitlist-related outcomes are associated with PEth test results. Patients with positive PEth tests were more likely to have unfavorable transplant waitlist-related outcomes. PEth testing has not been validated as a predictor of relapse to drinking in post-transplant patients and because its utility in the pre-transplant setting is unclear its use could lead to disparities in the selection of patients for liver transplantation.

Identifiants

pubmed: 35102553
doi: 10.1111/acer.14786
pmc: PMC9150771
mid: NIHMS1775776
doi:

Substances chimiques

Biomarkers 0
Glycerophospholipids 0
phosphatidylethanol 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

581-588

Subventions

Organisme : NIEHS NIH HHS
ID : P30 ES030283
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM113226
Pays : United States
Organisme : NIDDK NIH HHS
ID : L30 DK126211
Pays : United States
Organisme : NIAAA NIH HHS
ID : U01 AA026936
Pays : United States
Organisme : NIDDK NIH HHS
ID : K08 DK123381
Pays : United States
Organisme : NIAAA NIH HHS
ID : K23 AA029198
Pays : United States

Informations de copyright

© 2022 by the Research Society on Alcoholism.

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Auteurs

Claire S Faulkner (CS)

Department of Medicine, University of Arizona, College of Medicine, Phoenix, Arizona, USA.
Department of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha, Nebraska, USA.

Collin M White (CM)

Department of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Division of Gastroenterology, Hepatology and Nutrition, University of Louisville, Louisville, Kentucky, USA.

Wuttiporn Manatsathit (W)

Department of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha, Nebraska, USA.

Bernadette Lamb (B)

Department of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha, Nebraska, USA.

Vatsalya Vatsalya (V)

Division of Gastroenterology, Hepatology and Nutrition, University of Louisville, Louisville, Kentucky, USA.
University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky, USA.
Robley Rex VA Medical Center, Louisville, Kentucky, USA.
Hepatobiology and Toxicology Program, University of Louisville, Louisville, Kentucky, USA.

Craig J McClain (CJ)

Division of Gastroenterology, Hepatology and Nutrition, University of Louisville, Louisville, Kentucky, USA.
University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky, USA.
Robley Rex VA Medical Center, Louisville, Kentucky, USA.
Hepatobiology and Toxicology Program, University of Louisville, Louisville, Kentucky, USA.
Department of Pharmacology and Toxicology, University of Louisville, Louisville, Kentucky, USA.

Loretta L Jophlin (LL)

Department of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Division of Gastroenterology, Hepatology and Nutrition, University of Louisville, Louisville, Kentucky, USA.
University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky, USA.
Hepatobiology and Toxicology Program, University of Louisville, Louisville, Kentucky, USA.

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