To conduct a prospective, multicenter, observational study of patients with well-characterized alcoholic hepatitis (AH) and frequency matched individuals (by age, gender, and race) with comparable history of alcohol consumption but no clinical evidence of liver disease (controls). At the end of the study, a robust clinical information, central bio-repository will be developed from both cases and controls.
Study Type
OBSERVATIONAL
Enrollment
454
Mayo Clinic
Rochester, Minnesota, United States
Virginia Commonwealth University
Richmond, Virginia, United States
Developing a repository of biological samples from AH patients and heavy drinking controls.
To conduct a prospective, multicenter, observational study of patients with well-characterized AH and frequency matched individuals (by age, gender, and race) with comparable history of alcohol consumption but no clinical evidence of liver disease (controls). At the end of the study, a robust clinical information, central bio-repository of serum/plasma, peripheral mononuclear cells, genomic DNA, stool samples, urine, and liver tissue (where available) will be developed from both cases and controls.
Time frame: Up to 1 year
Characterizing AH subjects and controls to serve as the foundation for novel mechanistic and therapeutic studies.
Time frame: Up to 1 year
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