AlcHepNet Observational Study Eligibility and Enrollment

Eligibility information
Ages Eligible for Study:   21 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample

Study Population

Any subject with Alcoholic hepatitis, Heavy healthy drinkers, and Healthy controls

Criteria

CASES: Heavy drinkers with alcoholic hepatitis

Inclusion criteria

  1. A clinical diagnosis of alcoholic hepatitis
  2. Serum total bilirubin >3 mg/dL
  3. Subject or guardian ability to understand and willingness to provide written consent
  4. Age greater or equal to 21 years
  5. Re-enrolment of an alcoholic hepatitis donor is permissible up to 4 times if the donor presents with a new episode of alcoholic hepatitis 24 weeks or longer after the most recent enrolment in the study

Exclusion criteria

  1. Liver disease significantly caused by hemochromatosis, autoimmune liver disease, Wilson disease, NAFLD, and acute viral hepatitis
  2. (NOTE: The presence of chronic hepatitis C, hepatitis B, or HIV is not exclusion to participation.) Pregnant or breast feeding Based on the judgment of the investigator, subject is not capable of understanding or complying with the study requirements.

CONTROLS: Heavy drinkers without significant liver disease

Inclusion criteria

  1. History of chronic alcohol consumption sufficient to cause liver damage. Generally, this is considered to be >40 g/day or >280g/week on average for women and >60 g/day or >420 g/week on average for men, for many years (usually decades). Judgement about chronic alcohol consumption will be made by the site investigator.
  2. Subject or guardian ability to understand and willingness to provide written consent
  3. Age greater or equal to 21 years

Exclusion criteria

  1. Past evidence of alcoholic liver disease, defined as a bilirubin > 2.0 mg/dL, an AST > 1.5 ULN, and any hospital admission for liver disease, or the presence of esophageal varices or ascites (at any time in the past).
  2. Liver disease significantly caused by hemochromatosis, autoimmune liver disease, Wilson disease, NAFLD, and acute viral hepatitis (NOTE: The presence of chronic hepatitis C, hepatitis B, or HIV is not exclusion to participation.)
  3. Alcohol intake at less than 40 g/day or 280g/week on average for women and 60 g/day or 420 g/week on average for men for longer than the past 28 days
  4. If liver stiffness has been assessed within the prior 90 days, then stiffness suggesting fibrosis of F1 or greater is excluded. For Fibroscan, this is a fibrosis score >7.0 kPa.
  5. Pregnant or breast feeding
  6. Any of the following laboratory abnormalities within 90 days prior to signing the consent.

    1. Total bilirubin: >ULN*
    2. INR: > 1.4 5

      *Individuals with a diagnosis of Gilbert's can have total bilirubin up to 3.0 mg/dL and still be eligible for participation.

Healthy Controls

Inclusion criteria

  1. AUDIT-C scores of <4 for men and <3 for women (signifying no alcohol misuse)
  2. Abstinent (consumption of less than one standard drink/week) during the 6 months prior to enrolment
  3. Ability to understand and willingness to provide written consent.

Exclusion criteria

  1. Clinical history or laboratory evidence of liver disease including alcoholic liver disease, NAFLD, hemochromatosis, alcoholic hepatitis, autoimmune liver disease, Wilson disease, hepatitis C, or hepatitis B.
  2. Presence of diabetes (requiring treatment with oral agents or insulin).
  3. Significant heart disease (prior history of heart disease, other than hypertension)
  4. Chronic lung disease (requiring chronic treatment)
  5. Immune related conditions (such as Crohn's disease, rheumatoid arthritis, ulcerative colitis, systemic lupus erythematosus, severe psoriasis, etc.)
  6. Known infection with HIV
  7. Presumed infection, or use of antibiotics or other medications (e.g., corticosteroids) that would affect immune function, within the past 14 days
  8. BMI>35
  9. Current or known history of cancer (except in situ carcinoma of the cervix or adequately treated basal or squamous cell carcinoma of the skin) within 5 years prior to enrollment
  10. Pregnant or breast feeding
  11. Any of the following laboratory abnormalities within 90 days prior to signing the consent.

    1. Hemoglobin: <10 g/dL
    2. Conjugated bilirubin: > ULN
    3. INR: > 1.4
    4. AST: >40 IU/mL
    5. ALT: >40 IU/mL
  12. Based on the judgment of the investigator, subject is not capable of complying with the study requirements


AlcHepNet Organizations


AlcHepNet is a clinical and translational research initiative funded by the National Institute on Alcohol Abuse and Alcoholism (NIAAA), a division of NIH.