Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
JCR Impact Factor (IF) – 1.736
5-Year Impact Factor – 2.135
Index Copernicus  – 168.52
MEiN – 70 pts

ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
Periodicity – monthly

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Advances in Clinical and Experimental Medicine

2015, vol. 24, nr 5, September-October, p. 823–827

doi: 10.17219/acem/28485

Publication type: original article

Language: English

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The Distribution of Liver Steatosis, Fibrosis, Steatohepatitis and Inflammation Activity in Alcoholics According to FibroMax Test

Monika Gudowska1,A,D, Ewa Wojtowicz2,B,C, Bogdan Cylwik3,E, Ewa Gruszewska1,B,C, Lech Chrostek1,F

1 Department of Biochemical Diagnostics, Medical University in Białystok, Poland

2 Novencia Pharma, Warszawa, Poland

3 Department of Pediatric Laboratory Diagnostics, Medical University in Białystok, Poland


Background. The diagnosis of alcoholic liver diseases is based on the history of alcohol abuse, clinical evidence of liver disease and laboratory abnormalities. The new non-invasive biomarkers have higher sensitivity to quantify and predict steatosis and fibrosis than ultrasonography.
Objectives. The aim of this study was to evaluate the prevalence of liver diseases in alcoholics by means of FibroMax.
Material and Methods. A total of 142 consecutive alcoholics were enrolled in the study. The prevalence of liver diseases was assayed by means of non-invasive biomarkers: fibrosis by FibroTest, steatosis by SteatoTest, steatohapatitis by AshTest (alcoholic origin) and NashTest (non-alcoholic origin) and necroinflammatory activity by ActiTest.
Results. 38.7% of alcoholics do not have fibrosis, 38% – steatosis, 94.1% – alcoholic steatohepatitis, 56.6% – non-alcoholic steatohepatitis and 33.6% – necroinflammatory activity. The insignificant fibrosis (F < 2) is present in 37.2%, advanced (F ≥ 2) – 15.3% and cirrhosis (F4) – in 8.8%. Insignificant steatosis (S < 2) is observed in 31.3% and advanced (S ≥ 2) in 30.5%. Minimal alcoholic steatohepatitis (H1) exists in 5.2% patients, moderate (H2) in none of the patient and severe (H3) in only one patient (0.7%). The distribution of NashTest scores is as following: N0 – 56.6%, N1 – 38.2% and N2 – 5.1%. Insignificant inflammatory activity (A < 2) is present in 40.8% of alcoholic patients but significant (A ≥ 2) in 25.5%. The frequency of severe steatosis (F3) and necroinflammatory activity (A3) in patients with cirrhosis (F4) is 50% for each of them.
Conclusion. The prevalence of advanced fibrosis and cirrhosis evaluated by means of FibroMax in alcoholics is higher than in alcoholic liver disease (ALD) and lower than in mixed, alcoholic and non-alcoholic ones. This may indicate the presence of non-alcoholic liver disease in alcoholics.

Key words

non-invasive biomarkers, alcoholic liver diseases, FibroMax

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