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

  • John B. Whitfield
  • , Steven Masson
  • , Suthat Liangpunsakul
  • , Jessica Hyman
  • , Sebastian Mueller
  • , Guruprasad Aithal
  • , Florian Eyer
  • , Dermot Gleeson
  • , Andrew Thompson
  • , Felix Stickel
  • , Michael Soyka
  • , Ann K. Daly
  • , Heather J. Cordell
  • , Tiebing Liang
  • , Tatiana Foroud
  • , Lawrence Lumeng
  • , Munir Pirmohamed
  • , Bertrand Nalpas
  • , Camille Bence
  • , Jean Marc Jacquet
  • Alexandre Louvet, Romain Moirand, Pierre Nahon, Sylvie Naveau, Pascal Perney, Philippe Podevin, Paul S. Haber, Helmut K. Seitz, Christopher P. Day, Philippe Mathurin, Timothy M. Morgan, Devanshi Seth
  • Queensland Institute of Medical Research
  • Royal Victoria Infirmary
  • Indiana University Bloomington
  • The Centenary Institute
  • Heidelberg University
  • QueensMedical Centre
  • Royal Hallamshire Hospital
  • University of Liverpool
  • University Hospital Zurich
  • Privatklinik Meiringen
  • CHU Caremeau
  • INSERM U70
  • CHRU Roger Salengro
  • Centre Hospitalier Universitaire Régional Montpellier
  • Service de Neurochirurgie
  • Jean Verdier Hospital
  • University of Paris 13
  • Inserm U1162 “Functional Genomics of Solid Tumors”
  • HU-Paris Sud
  • AP-HP
  • Royal Prince Alfred Hospital
  • University of Sydney
  • VA Long Beach Healthcare System

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

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.

Original languageEnglish
Pages (from-to)1-7
Number of pages7
JournalAlcohol
Volume66
DOIs
StatePublished - Feb 2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Abstinence
  • Alcohol
  • Aspartate aminotransferase
  • Cirrhosis
  • Gamma glutamyl transferase

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