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PiMZ Longitudinal Cohort (PiMZ Logic)

RECRUITINGSponsored by Columbia University
Actively Recruiting
SponsorColumbia University
Started2025-05-30
Est. completion2029-02
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations5 sites

Summary

Alpha-1 Anti-trypsin Deficiency (AATD) is a genetic disease with lung and liver disease presentations. Presentations are variable in the heterozygous population, the most predominant genotype being PiMZ. The purpose of this study in PiMZ heterozygous patients is to examine the density of the lung as measured by chest computed tomography (CT) and determine if existing emphysema predicts changes in the rate of subsequent emphysema or changes in CT, serum or plasma biomarkers of interest. The overarching goal is to develop biomarkers pertinent to the PiMZ patient that can be used in interventional trials since lung function changes do not typically inform disease progression in AATD.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

1. Males and females aged 18 years and older
2. Understand the study procedures, risks, benefits, purpose
3. Able and willing to comply with the study procedures
4. Have PiMZ alpha-1 antitrypsin deficiency
5. Post bronchodilator FEV1 \< 80% predicted AND post bronchodilator FEV1/FVC \< 70%
6. Be an existing member of the Alpha-1 Foundation Clinical Cohort (also known as the Alpha-1 Foundation Research Registry)
7. Agree to have the data collected in this study be shared with the Alpha-1 Foundation Research Registry

Exclusion Criteria:

1. AATD non-PiMZ status, including carriers
2. Current lung, hematologic, or solid organ malignancy other than skin or cervical Stage 1 cancers within the past 3 years
3. COPD exacerbation or other pulmonary infection within 6 weeks of baseline visit
4. Pregnancy at the time of the screening visit
5. Inability to lie still in a supine position for 15 minutes during CT acquisition
6. Inability to perform quality-controlled lung function testing
7. Allergy to albuterol
8. Currently receiving intravenous or subcutaneous immunoglobulin for any disease state
9. Past or present major surgery on the lungs including pneumonectomy or lobectomy. Wedge resections, past segmentectomy, and pleurodesis surgeries are allowed.
10. Previous lung or liver transplantation or currently on the transplant list
11. Decompensated cirrhosis
12. Current presence of endobronchial coils or valves in the lung
13. Clinically significant bronchiectasis as defined by the investigator. In general, this would exclude patients with chronic infection of the lungs requiring treatment within the past 6 months including non-tuberculous mycobacterial disease, chronic fungal disease, allergic bronchopulmonary aspergillosis, or known colonization of bronchiectasis with pseudomonas or stenotrophomonas species.
14. Participation in the active treatment arm of a therapeutic clinical trial at baseline visit unless using one of the Alpha-1 augmentation therapies in alternative doses.
15. Patient with Automatic Implantable Cardioverter Defibrillator (AICD) and permanent pacemakers (PPM)
16. Patient receiving biologic immunomodulators that will affect the assessment of the serum biomarkers (as determined by the site PI)
17. Patient with pleural catheters
18. Any condition that in the opinion of the investigator might adversely influence the study outcome

Conditions4

Alpha 1-Antitrypsin DeficiencyCOPDEmphysema or COPDLiver Disease

Locations5 sites

Alabama

1 site
University of Alabama at Birmingham
Birmingham, Alabama, 35233
Dianne Freeman, BS, RRT205-996-2709dsmurphy@uabmc.edu

California

1 site
University of California- Los Angeles
Los Angeles, California, 90095
Semi Yoon310-794-2156semiyoon0113@g.ucla.edu

Colorado

1 site
National Jewish Health
Denver, Colorado, 80206
Robert Sandhaus, MD, PhD, FCCPRSandhaus@alphanet.org

Illinois

1 site
University of Chicago
Chicago, Illinois, 60637
Vanita Patel773-702-1012vpatel4@bsd.uchicago.edu

New York

1 site
Columbia University Irving Medical Center
New York, New York, 10032
Sabrina Palumbo, BS212-305-3745sp4461@cumc.columbia.edu

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