Actively Recruiting
Study of Alcohol-related Liver Disease in Europe
Led by University Hospital, Lille · Updated on 2022-03-17
7500
Participants Needed
1
Research Sites
573 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Alcohol-induced liver injury is made up of fatty liver, fibrosis and alcoholic hepatitis (AH), elementary lesions that may occur separately, simultaneously or sequentially in a same patient. Among these histological features, alcoholic hepatitis, a necro-inflammatory process is associated with the fastest fibrosis progression leading to cirrhosis in 40% of cases and a pivotal lesion driving increased risk of liver decompensation. The non-invasive methods for the diagnosis of fibrosis open new perspectives for a better understanding of the natural history of disease-progression from early injury to the cirrhotic stage, for the identification of subgroup patients at risk of developing cirrhosis at medium term and for proposing a strategy of screening of patients with extensive cirrhosis at risk of liver-threatening events. There is an urgent need to perform studies in asymptomatic heavy drinkers in order to identify cut-offs associated with significant risk of development of cirrhosis at medium term. Such objectives require large-scale screening of heavy drinkers. Each of non-invasive methods have been tested to predict with of extensive fibrosis with a high predictive performance as shown below. A screening policy cannot be accepted without answering the following questions: a) are the requirements of public health screening fulfilled? b) Is the group of patients undergoing screening defined? c) is there a reliable method for of testing? Indeed, the detection of a disease is subject to certain public health requirements and may be proposed to health authorities only if it modifies the management of subjects screened. In the specific case of mass screening of liver fibrosis in heavy drinkers, only the detection of extensive fibrosis could fulfill this criterion because of the potential survival benefit resulting from the screening of hepatocellular carcinoma (HCC) in patients with extensive fibrosis. Indeed, recent studies have found that the probability of receiving curative treatment of HCC was significantly higher in patients who received a six-month surveillance ultrasound. Therefore, the detection of extensive fibrosis seems reasonable in the light of these studies when considering that the yearly risk of development of HCC in the subgroup of heavy drinkers with extensive fibrosis is approximately 3%. Taking into account the above scientific arguments, the most recent EASL clinical practical guidelines on ALD recommend longitudinal studies using non-invasive tools to evaluate screening of extensive fibrosis and disease progression in heavy drinkers.
CONDITIONS
Official Title
Study of Alcohol-related Liver Disease in Europe
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Active excessive alcohol consumption defined as more than 210 g per week for men and more than 140 g per week for women during the previous year
- Patients with high risk of alcoholic-related liver disease with available assessments including abdominal ultrasound, FibroScan�, FibroTest�, AshTest�, LCR1-LCR2�, or other non-patented methods like Forns Index, Fib-4, Hepascore�
- For patients with uninterpretable liver stiffness measurements, inclusion allowed if FibroTest� and LCR1 and LCR2 measurements are available
- Patients must provide written informed consent and agree to blood and tissue storage if biopsy is performed
- Patients agree to participate in at least a 5-year follow-up
- Patients must have social insurance
You will not qualify if you...
- Evidence of other known chronic liver diseases including positive hepatitis B surface antigen, hepatitis C virus infection, autoimmune liver disease, or known/suspected hepatocellular carcinoma
- Any previous episode of decompensated liver disease such as ascites, hepatic encephalopathy, or variceal bleeding before inclusion
- Known HIV infection
- Terminal extrahepatic illnesses limiting functional status such as heart failure, renal failure, neurological or respiratory diseases
- Medical conditions expected to reduce life expectancy to less than 2 years
- Known extra-hepatic cancers except basal cell skin cancer
- Conditions that impede study completion such as homelessness or non-compliance
- Mental instability or incompetence affecting informed consent validity
- Lack of informed consent or refusal to participate in follow-up
- Conditions increasing risk from repeated blood draws like hemophilia or severe coagulation disorders
- Pregnant or lactating women
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hop Claude Huriez Chu Lille
Lille, France, 59037
Actively Recruiting
Research Team
P
Philippe Mathurin, MD,PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
5
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