Study of Genetic Determinants in Alcoholic Hepatitis and Establishment of a Multicenter Prospective Cohort of Patients With Alcoholic Liver Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Lille

About this trial

Alcoholic hepatitis carries a risk of high mortality at short term, especially in its severe form. Its diagnosis is confirmed by liver biopsy. The prevalence of alcoholic hepatitis, severe or not severe, is poorly known and prospective data are needed. The present observational study aims to define the prevalence of alcoholic hepatitis among patients admitted for jaundice and determine their outcome according to the severity. Survival and markers of liver dysfunction will be assessed. A biobank including genetic samples will be created to identify the disease profile in terms of inflammation and regeneration. The performance of non-invasive criteria for diagnosis will also be studied.

Eligibility criteria

Qualifiers

On average> 40 g / day for women and 50 g / day for men

Duration:> 5 years

Recent jaundice episode (less than 3 months)

Bilirubin> 50 mg / l (85μmol / l)

Disqualifiers

Presence of another hepatic pathology: evidenced by blood biology, imaging or histology (viral or autoimmune hepatitis, hemochromatosis, Wilson's disease)

Presence of hepatocellular carcinoma

HIV infection

History established / suggestive of HAA (Clinical, biological and / or histological criteria) in particular absence of jaundice episode

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

447 Participants
are grouped into 3 trial groups

Sponsors and collaborators