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.
Study Type
OBSERVATIONAL
Enrollment
447
Chr Angers
Angers, France
RECRUITINGChru Besancon
Besançon, France
RECRUITINGHôpital Jean Verdier, AH-HP
Bondy, France
RECRUITINGCentre Hospitalier Universitaire
Caen, France
RECRUITINGHopital Nord - Chu38 - La Tronche
La Tronche, France
RECRUITINGHôpital Claude Huriez, CHU
Lille, France
RECRUITINGAssociation Hopital Saint Joseph - Marseille
Marseille, France
RECRUITINGChu Montpellier
Montpellier, France
RECRUITINGHu Est Parisien Site St Antoine Aphp - Paris 12
Paris, France
RECRUITINGPrevalence of alcoholic hepatitis in heavy drinkers with jaundice
Assess the prevalence of biopsy-proven alcoholic hepatitis in a cohort of heavy drinkers admitted with recent jaundice
Time frame: At baseline (time of liver biopsy)
Survival
Survival rate at 12 months
Time frame: at 12 months
Change in serum total bilirubin
Total bilirubin is a liver parameter, used for the biological liver test evaluation, measured in mg/dl in the serum
Time frame: Baseline, at 7 days, at 30 days, at 3 months at 6 months and at 12 months
Change in serum creatinine
Creatinine is a marker of kidney function, assessed in the blood and measured in milligrams per deciliter
Time frame: Baseline, at 7 days, at 30 days, at 3 months at 6 months and at 12 months
Change in MELD (Model for End-stage Liver Disease)score
The MELD score is a validated tool based on INR, creatinine and bilirubin measured in the blood with the following formula:(9.57 × log creatinine in milligrams per deciliter) + (3.78 × log bilirubin in milligrams per deciliter) + (11.20 × log international normalized ratio) + 6.43. The MELD score is used in liver disorders to assess the degree of liver failure. It has no unit.
Time frame: Baseline, at 7 days, at 30 days, at 3 months at 6 months and at 12 months
Identification of inflammatory and biochemical profiles of patients with severe, non-severe and cirrhotic alcoholic hepatitis, based on the constitution of a biobank (serum and plasma)
Serum and plasma evaluation of translational markers (e.g. cytokines) associated with inflammation in patients with alcohol-related liver disease. The list of markers which will be assessed cannot be determined at present and will depend on other ongoing studies performed in alcoholic hepatitis.
Time frame: Baseline, at 7 days, at 30 days and at 12 months
Identification of the genetic profiles of individuals with severe, non-severe and cirrhotic alcoholic hepatitis( blood sample)
Evaluation of genetic markers associated with alcoholic hepatitis as compared to patients with alcohol-related liver disease without alcoholic hepatitis. We will use a non a priori approach as recommended in genetic studies. Thus, the list of genetic markers cannot be provided at that time.
Time frame: Baseline
Measurement of diagnostic performance (area under the ROC curve)
Measurement of diagnostic performance (area under the ROC curve) of the simple and non-invasive clinical and biological criteria for alcoholic hepatitis proposed in an international expert opinion
Time frame: At baseline
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