Hidden liver harm: study tracks silent damage in genetic disorder
NCT ID NCT02014415
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study follows 120 adults with Alpha-1 Antitrypsin Deficiency, a genetic condition that can cause lung and liver problems. Researchers use liver biopsies and genetic samples over 5 years to find out who develops liver scarring or cirrhosis and why. The goal is to identify risk factors that are currently overlooked.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could reveal why some people with Alpha-1 Antitrypsin Deficiency develop serious liver disease while others do not, pointing toward future prevention or treatment strategies.
- What could go wrong
- This is an observational study, not a treatment trial, so it will not directly help participants. It is small (120 people) and may not uncover clear genetic or environmental factors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Dec 2013
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Pi-ZZ AAT deficient adults with either no previous history of liver disease, moderate-severe liver disease or post liver transplant. Biologic family members who are also Pi-ZZ and ≥ 18 years of age, will be offered enrollment into the study. The purpose of including family members is to determine if the natural history of the liver disease is consistent in a given family.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Liver Biopsy Group: Inclusion Criteria * Adults (≥ 18 years of age), with Alpha-1 Antitrypsin Deficiency * Documented evidence Pi-ZZ phenotype or genotype * Both genders, all races and ethnic groups * Willingness to be followed for up to 5 years Exclusion Criteria: * Evidence of advanced liver disease defined by Child-Pugh Class B or C (score ≥ 7) * Known advanced lung disease defined as forced expiratory volume at one second (FEV1) \< 40 % of Predicted * History of Organ Transplantation * Known congenital or metabolic liver disease (e.g.: Wilson's, glycogen storage, cystic fibrosis)or iron overload as evidenced by ≥ Grade 3 iron staining on a previous liver biopsy * Evidence of chronic hepatitis B (marked by the presence of HBsAg in serum) or Hepatitis C (marked by the presence of anti-hepatitis C virus (HCV) or HCV RNA in serum) * Vascular disorders of the liver (e.g.: cardiac sclerosis, acute or chronic Budd-Chiari, hepatoportal sclerosis, peliosis) * Known HIV positivity * Diagnosis of malignancy within the last 5 years * Active substance abuse, that in the opinion of the study investigator, would interfere with adherence to study requirements * Concomitant severe underlying systemic illness or medical condition which in the opinion of the investigator, would make the patient unsuitable for the study or would interfere with completion of follow-up * Inability to comply with the longitudinal follow-up as outlined in the protocol * Failure of the participant to sign informed consent or Health Insurance Portability and Accountability Act (HIPAA) documents Known Severe Liver Disease Group: Inclusion Criteria * Adults (≥ 18 years of age), with alpha-1-antitrypsin deficiency * Documented evidence PI-ZZ phenotype or genotype * Documented evidence of portal hypertension or evidence of advanced liver disease defined by Child-Pugh Class B or C (score ≥ 7), or previous liver biopsy with an Ishak Fibrosis Score ≥ 4 * Both genders, all races and ethnic groups * Willingness to be followed for up to 5 years Exclusion Criteria * History of Organ Transplantation * Known congenital or metabolic liver disease (e.g.: Wilson's, glycogen storage, cystic fibrosis) and iron overload as evidenced by ≥ Grade 3 iron staining on a previous liver biopsy * Evidence of chronic hepatitis B (marked by the presence of HBsAg in serum) or Hepatitis C (marked by the presence of anti-HCV or HCV RNA in serum) * Vascular disorders of the liver (e.g.: cardiac sclerosis, acute or chronic Budd-Chiari, hepatoportal sclerosis, peliosis) * Known HIV positivity * Diagnosis of malignancy within the last 5 years which in the opinion of the investigator, would make the patient's follow-up problematic or the results uninterpretable. * Active substance abuse, that in the opinion of the study investigator, would interfere with adherence to study requirements * Concomitant severe underlying systemic illness or medical condition which in the opinion of the investigator, would make the patient unsuitable for the study or would interfere with completion of follow-up * Inability to comply with the longitudinal follow-up as outlined in the protocol * Failure of the participant to sign informed consent or HIPAA documents. Post Liver Transplant Group Inclusion Criteria * Adults (≥ 18 years of age), with alpha-1-antitrypsin deficiency * Pre-transplant documented evidence of PI-ZZ phenotype or genotype * Documented evidence of liver transplantation * Both genders, all races and ethnic groups Exclusion Criteria * Active substance abuse, that in the opinion of the study investigator, would interfere with adherence to study requirements * Concomitant severe underlying systemic illness or medical condition which in the opinion of the investigator, would make the patient unsuitable for the study or would interfere with completion of study requirements * Failure of the participant to sign informed consent or HIPAA documents.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Boston University School of Medicine
Boston, Massachusetts, 02118, United States
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Saint Louis University
St Louis, Missouri, 63104, United States
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University of California
San Diego, California, 92103, United States
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