Literature DB >> 29277282

Evaluation of laboratory tests for cirrhosis and for alcohol use, in the context of alcoholic cirrhosis.

John B Whitfield1, Steven Masson2, Suthat Liangpunsakul3, Jessica Hyman4, Sebastian Mueller5, Guruprasad Aithal6, Florian Eyer7, Dermot Gleeson8, Andrew Thompson9, Felix Stickel10, Michael Soyka11, Ann K Daly2, Heather J Cordell12, Tiebing Liang3, Tatiana Foroud3, Lawrence Lumeng3, Munir Pirmohamed9, Bertrand Nalpas13, Camille Bence14, Jean-Marc Jacquet15, Alexandre Louvet14, Romain Moirand16, Pierre Nahon17, Sylvie Naveau18, Pascal Perney19, Philippe Podevin20, Paul S Haber21, Helmut K Seitz5, Christopher P Day2, Philippe Mathurin14, Timothy M Morgan22, Devanshi Seth23.   

Abstract

Laboratory tests can play an important role in assessment of alcoholic patients, including for evaluation of liver damage and as markers of alcohol intake. Evidence on test performance should lead to better selection of appropriate tests and improved interpretation of results. We compared laboratory test results from 1578 patients between cases (with alcoholic cirrhosis; 753 men, 243 women) and controls (with equivalent lifetime alcohol intake but no liver disease; 439 men, 143 women). Comparisons were also made between 631 cases who had reportedly been abstinent from alcohol for over 60 days and 364 who had not. ROC curve analysis was used to estimate and compare tests' ability to distinguish patients with and without cirrhosis, and abstinent and drinking cases. The best tests for presence of cirrhosis were INR and bilirubin, with areas under the ROC curve (AUCs) of 0.91 ± 0.01 and 0.88 ± 0.01, respectively. Confining analysis to patients with no current or previous ascites gave AUCs of 0.88 ± 0.01 for INR and 0.85 ± 0.01 for bilirubin. GGT and AST showed discrimination between abstinence and recent drinking in patients with cirrhosis, including those without ascites, when appropriate (and for GGT, sex-specific) limits were used. For AST, a cut-off limit of 85 units/L gave 90% specificity and 37% sensitivity. For GGT, cut-off limits of 288 units/L in men and 138 units/L in women gave 90% specificity for both and 40% sensitivity in men, 63% sensitivity in women. INR and bilirubin show the best separation between patients with alcoholic cirrhosis (with or without ascites) and control patients with similar lifetime alcohol exposure. Although AST and GGT are substantially increased by liver disease, they can give useful information on recent alcohol intake in patients with alcoholic cirrhosis when appropriate cut-off limits are used.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Abstinence; Alcohol; Aspartate aminotransferase; Cirrhosis; Gamma glutamyl transferase

Mesh:

Substances:

Year:  2017        PMID: 29277282      PMCID: PMC5745811          DOI: 10.1016/j.alcohol.2017.07.006

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  21 in total

Review 1.  Special considerations in interpreting liver function tests.

Authors:  D E Johnston
Journal:  Am Fam Physician       Date:  1999-04-15       Impact factor: 3.292

Review 2.  The validity of self-reports of alcohol consumption: state of the science and challenges for research.

Authors:  Frances K Del Boca; Jack Darkes
Journal:  Addiction       Date:  2003-12       Impact factor: 6.526

3.  Clinical performance of the carbohydrate-deficient transferrin (CDT) assay by the Sebia Capillarys2 system in case of cirrhosis. Interest of the Bio-Rad %CDT by HPLC test and Siemens N-Latex CDT kit as putative confirmatory methods.

Authors:  Philippe Gonzalo; Matthieu Pecquet; Chantal Bon; Sylvie Gonzalo; Sylvie Radenne; Claude Augustin-Normand; Jean-Christophe Souquet
Journal:  Clin Chim Acta       Date:  2012-01-08       Impact factor: 3.786

Review 4.  Biomarkers for detection of alcohol consumption in liver transplantation.

Authors:  Katharina Staufer; Michel Yegles
Journal:  World J Gastroenterol       Date:  2016-04-14       Impact factor: 5.742

5.  Relationship of Abnormal Chromatographic Pattern for Carbohydrate-Deficient Transferrin with Severe Liver Disease.

Authors:  Scott H Stewart; Adrian Reuben; Raymond F Anton
Journal:  Alcohol Alcohol       Date:  2016-10-07       Impact factor: 2.826

Review 6.  The model for end-stage liver disease (MELD).

Authors:  Patrick S Kamath; W Ray Kim
Journal:  Hepatology       Date:  2007-03       Impact factor: 17.425

7.  Serum carbohydrate-deficient transferrin as a marker of alcohol consumption in patients with chronic liver diseases.

Authors:  H Bell; C Tallaksen; T Sjåheim; R Weberg; N Raknerud; H Orjasaeter; K Try; E Haug
Journal:  Alcohol Clin Exp Res       Date:  1993-04       Impact factor: 3.455

Review 8.  Ethanol metabolites: their role in the assessment of alcohol intake.

Authors:  Friedrich M Wurst; Natasha Thon; Michel Yegles; Alexandra Schrück; Ulrich W Preuss; Wolfgang Weinmann
Journal:  Alcohol Clin Exp Res       Date:  2015-09-07       Impact factor: 3.455

9.  Brief report: genetics of alcoholic cirrhosis-GenomALC multinational study.

Authors:  John B Whitfield; Khairunnessa Rahman; Paul S Haber; Christopher P Day; Steven Masson; Ann K Daly; Heather J Cordell; Sebastian Mueller; Helmut K Seitz; Suthat Liangpunsakul; Chi Westerhold; Tiebing Liang; Lawrence Lumeng; Tatiana Foroud; Bertrand Nalpas; Philippe Mathurin; Felix Stickel; Michael Soyka; Gregory J Botwin; Timothy R Morgan; Devanshi Seth
Journal:  Alcohol Clin Exp Res       Date:  2015-05       Impact factor: 3.455

Review 10.  Biomarker-Based Approaches for Assessing Alcohol Use Disorders.

Authors:  Onni Niemelä
Journal:  Int J Environ Res Public Health       Date:  2016-01-27       Impact factor: 3.390

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  2 in total

1.  Serum metabolomic analysis reveals several novel metabolites in association with excessive alcohol use - an exploratory study.

Authors:  Danni Liu; Zhihong Yang; Kristina Chandler; Adepeju Oshodi; Ting Zhang; Jing Ma; Praveen Kusumanchi; Nazmul Huda; Laura Heathers; Kristina Perez; Kelsey Tyler; Ruth Ann Ross; Yanchao Jiang; Dabao Zhang; Min Zhang; Suthat Liangpunsakul
Journal:  Transl Res       Date:  2021-11-03       Impact factor: 10.171

2.  A Dynamic Aspartate-to-Alanine Aminotransferase Ratio Provides Valid Predictions of Incident Severe Liver Disease.

Authors:  Fredrik Åberg; Christopher J Danford; Maja Thiele; Mats Talbäck; Ditlev Nytoft Rasmussen; Z Gordon Jiang; Niklas Hammar; Patrik Nasr; Mattias Ekstedt; Anna But; Pauli Puukka; Aleksander Krag; Jouko Sundvall; Iris Erlund; Veikko Salomaa; Per Stål; Stergios Kechagias; Rolf Hultcrantz; Michelle Lai; Nezam Afdhal; Antti Jula; Satu Männistö; Annamari Lundqvist; Markus Perola; Martti Färkkilä; Hannes Hagström
Journal:  Hepatol Commun       Date:  2021-03-08
  2 in total

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