Enhanced liver fibrosis test in a group of patients with alcohol abuse

  • Ivica Avberšek-Lužnik Department of Laboratory Diagnostics, Jesenice general hospital, Jesenice, Slovenia
  • Branka Svetic Clinical laboratory, Community health centre, Medvode, Slovenia
  • Karmen Janša Department of diabetics, Jesenice general hospital, Jesenice, Slovenia
Keywords: alcoholism, liver fibrosis, noninvasive biomarkers of liver damege, ELF test

Abstract

Background: Enhanced Liver Fibrosis (ELF) test is a set of indirect markers of liver fibrosis that can be used for the assessment of the severity of liver fibrosis. ELF test includes three biomarkers: hyaluronic acid (a component of the extracellular matrix), TIMP-1 (an inhibitor of matrix metalloproteinases that break down collagen) and PIIINP (a marker of collagen synthesis at the site of disease process). These biomarkers or ELF test can be used in early diagnostic approaches of liver damage caused by viral infections or alcohol abuse. The main aim of our study was measuring ELF values in three groups of individuals: a control group, a group of alcoholics and a group of patients with acute alcohol intoxication. The results of ELF test were compared with established biochemical markers of alcoholism.

Methods: In the study 113 individuals (71 males, 42 females) with a mean age of 43 years were included. They were divided into three groups: OSM group consisted of individuals (N = 39) who were seen in the Occupational and Sports Medicine Clinic. The AAI group consisted of 31 individuals with acute alcohol intoxication, and the AD group consisted of 43 individuals who were undergoing treatment for alcohol dependence. We assessed the following parameters in the serum samples of all three groups of subjects: mean corpuscular volume (MCV), activity of aspartate amino transferase (AST), alanine amino transferase (ALT), gama glutamyl transferase (GGT) and the parameters of novel ELF test for liver fibrosis stage assessment. ELF values are below 7.7 in the early stage of fibrotic process and above 9.8 in severe fibrosis. All statistical tests were conducted by SPSS 21.0 for Windows (SPSS, Inc. Chicago, USA).

Results: Mean values of the established biomarkers of alcoholism in OSM, AAI and AD groups for MCV were 91.9; 90.9 in 95.3, medianes of catalitic activity of AST were 0.30; 033 in 0.42 µkat/L, for ALT 0.41; 0.34 in 0.56 µkat/L and for GGT 0.37; 0.34 in 0.92 µkat/L. Kruskal – Walliss test showed a statistical significance between groups for AST, GGT in MCV (p < 0.002), while ALT (p = 0.052) did not differ significantly. In OSM mediane ELF test is 7.99 (6.99–10.18), and in AD group 9.47 (6.98–14.73). In AD group a statistically significant correlation was between AST, ALT, GGT and ELF test (r = 0.524; 0.306 in 0.632), in OSM the significance was proved only for MCV (r = 0.327).

Conclusion: The results of the measurements show a statistically significant increase in the established markers of alcoholism (MCV, AST, ALT and GGT) in the AD group as compared to the OSM group. Median ELF test in the AD group indicates moderate liver fibrosis, however, considering the range of 6.98 to 14.73, some individuals in this group have severe fibrosis. The results show that increased values of AST, ALT and GGT and correlations between them indicate liver damage, while ELF test better predicts developing stage of liver fibrosis. Various scores and indexes are used for liver fibrosis assessment. ELF test is proposed as a very useful diagnostic test and probably has a high potential of aplicability in the primary care of patients with alcoholic and nonalcoholic liver damage.

Downloads

Download data is not yet available.

References

Mathurin P, Bataller R. Trends in the menagement and burden of alcoholic liver disease. J Hepatol. 2015; 62(1): 38-46.

Lombardi R, Buzzetti E, Roccarina D, Tsochatzis EA. Non-invasive assessment of liver fibrisis in patients with alcoholic liver disease. World J Gastroenterol. 2015; 21(39): 11044-52.

Karanjia RN, Crossey MME, Cox IJ, Fye HKS, Njie R, Goldin RD, et al. Hepatic steatosis and fibrosis: non-invasive assessment. World J Gastroenterol. 2016; 22(45): 9880-97.

Chrostek L, Panasiuk A. Liver fibrosis markers in alcoholic liver disease. World J Gastroenterol. 2014; 20: 8018-23.

Grigorescu M. Noninvasive biochemical markers of liver fibrosis. Journal of Gastrointestinal and Liver Diseases. 2006; 15(2): 149-59.

Bedossa P, Dargere D, Paradis V. Sampling variability of liver fibrosis in chronic hepatitis C. Hepatology. 2003; 38(6): 1449-57.

Guido M, Rugge M. Liver biopsy sampling in chronic viral hepatitis. Semin liver dis. 2004; 24(1): 89-97.

Parkes J, Guha IN, Harris S, Rosenberg WM, Roderick PJ. Systematic review of the diagnostic performance of serum markers of liver fibrosis in alcoholic liver disease. Comp Hepatol. 2012; 11(5): 1-15.

Lieber CS, Weiss DG, Paronetto F. Value of fibrosis markers for staging liver fibrosis in patients with precirrhotic alcoholic liver disease. Alcohol Clin Exp Res. 2008; 32: 1031-39.

Rosenberg WM, Voelker M, Thiel R, Becka M, Burt A, Schuppan D, et al. Serum markers detects the presence of liver fibrosis: a cohort study. Gastroenterology. 2004; 127: 1704-13.

Guéchot J, Laudat A, Loria A, Serfaty L, Poupon R, Giboudeau J. Diagnostic accuracy of hyaluronan and type III procollagen amino-terminal peptide serum assays as markers of liver fibrosis in chronic viral hepatitis C evaluated by ROC curve analysis. Clinical chemistry. 1996; 42(4): 558-63.

Niemelä O, Risteli L, Parkkinen J, Risteli J. Purification and characterization of the N-terminal propeptide of human type III procollagen. Biochemical Journal. 1985; 232(1): 145-50.

Walsh KM, Timms P, Campbell S, Norman R, Macsween M, Morris AJ. Plasma levels of matrix metalloproteinase-2 (MMP-2) and tissue inhibitors of metalloproteinases-1 and-2 (TIMP-1 and TIMP-2) as noninvasive markers of liver disease in chronic hepatitis C comparison using ROC analysis. Digestive diseases and sciences. 1999; 44(3): 624-30.

Trépo E, Potthoff A, Pradat P, Bakshi R, Young B, Lagier R, et al. Role of a cirrhosis risk score for the early prediction of fibrosis progression in hepatitis C patients with minimal liver disease. Journal of hepatology. 2011; 55(1): 38-44.

Guéchot J, Trocmé C, Renversez JC, P Zarski JP. Independent validation of the Enhanced Liver Fibrosis (ELF) score in the ANRS HC EP 23 Fibrostar cohort of patients with chronic hepatitis C. Clinical Chemistry and Laboratory Medicine. 2012; 50(4): 693-99.

Parkes J, Roderick P, Harris S, Day C, Mutimer D, Collier J, et al. Enhanced liver fibrosis test can predict clinical outcomes in patients with chronic liver disease. Gut. 2010; 59(9): 1245-51.

Stevenson M, Lloyd-Jones M, Morgan MY, Wong R. Non-invasive diagnostic assessment tools for the detection of liver fibrosis in patients with suspected alcohol-related liver disease: a systematic review and economic evaluation. Health Technol Assess. 2012; 16(4): 1-174.

Luire Y, Webb M, Cytter-Kuint R, Shteingart S, Lederkremer GZ. Non-invasive diagnosis of liver fibrossis and cirrhosis. World J Gastroenterol. 2015; 21(41): 11567-83.

Sharma S, Khalili K, Nguyen C. Non-invasive diagnosis of advanced fibrosis and cirrhosis. World J Gastroenterol. 2014; 20(45): 16820-30.

Angulo P. Keach JC, Batts KP, Lindor KD. Independent predictors of liver fibrosis in patients with nonalcoholic steatohepatitis. Hepatology 1999; 30: 1356–62.

Dinevski D, Povalej P, Kravos M. Intelligent data analysis for the diagnosis of alcohol dependence syndrome. J Intern Med research. 2011; 988 -1000.

Gough G, Heathers L, Puckett D, Westerhold C, Ren X, Zhangsheng Yu, et al. The utility of commonly used laboratory tests to screen for excessive alcohol use in clinical practice. Alcohol Clin Exp Res. 2015; 39(8): 1493–1500.

Guha IN, Parkes J, Roderick P, Chattopadhyay D, Cross R, Harris R, et al., Noninvasive markers of fibrosis in nonalcoholic fatty liver disease: Validating the European Liver Fibrosis Panel and exploring simple markers. Hepatology. 2008; 47(2): 455-60.

Gangadharan B, Antrobus R, Dwek RA, Zitzmann N. Novel serum biomarker candidates for liver fibrosis in hepatitis C patients. Clinical chemistry. 2007; 53(10): 1792-99.

Friedrich-Rust M, Rosenberg W, Parkes J, Herrmann E, Zeuzen S, Sarrazin C. Comparison of ELF, FibroTest and FibroScan for the non-invasive assessment of liver fibrosis. BMC gastroenterology. 2010; 10(1): 1-8.

Parkes J, Roderick P, Harris S, Day C, Mutimer D, Collier J, et al. Enhanced liver fibrosis test can predict clinical outcomes in patients with chronic liver disease. Gut. 2010; 59: 1245-51.

Published
2019-05-31
How to Cite
1.
Avberšek-Lužnik I, Svetic B, Janša K. Enhanced liver fibrosis test in a group of patients with alcohol abuse. TEST ZdravVestn [Internet]. 31May2019 [cited 25Apr.2024];88(5-6):213-24. Available from: http://vestnik-dev.szd.si/index.php/ZdravVest/article/view/2690
Section
Original article