Alpha-1 Antitrypsin Deficiency
Conditions
Keywords
Alpha 1-Antitrypsin Deficiency
Brief summary
Individuals with a deficiency of alpha-1 antitrypsin (AAT) often develop emphysema. Traditional lung function tests may not be the most accurate way to measure the progression of emphysema. This study will compare high resolution computed tomography (CT) scans to spirometry to measure the progression of emphysema.
Detailed description
AAT deficiency is a genetic disorder associated with emphysema. Spirometry, the lung function test that measures how well the lungs exhale air, is used to diagnose and track the progression of emphysema. Some studies have suggested that forced expiratory volume in 1 second (FEV1) measurements, a type of spirometry test, may lack accuracy in detecting disease progression in cases of severe AAT deficiency. Another method, high resolution chest CT scans, may be more accurate at measuring the progression of emphysema. The purpose of this study is to determine if high resolution CT scans are better at detecting the progression of emphysema than lung function tests. Results from this study may lead to the development of a more accurate way to assess lung tissue loss and may improve the understanding of lung destruction in AAT deficiency. This study will last 4 years and will enroll people with AAT deficiency who have nearly normal lung function test results. Study visits, each lasting about 4 hours, will occur at baseline and months 6, 12, 18, 24, and 36. At each visit, participants will undergo lung function tests, a CT scan, blood collection, and a physical exam. Female participants will have urine collected for a pregnancy test. All participants will also complete questionnaires to assess health status and lung function. Study researchers will call participants every 2 months to collect information on lung disease symptoms and medication changes.
Interventions
None listed
Sponsors
National Center for Research Resources (NCRR)
Alpha-1 Foundation
Medical University of South Carolina
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Diagnosis of AAT deficiency, as determined by both of the following conditions: 1. Serum A1-P1 levels less than 11uM or 80 mg/dL 2. Protease inhibitor phenotype Z (PiZZ) or Znull phenotype confirmed by gene probe analysis. Previous serum levels and phenotype results are acceptable if documented from a Clinical Laboratory Improvement Amendments (CLIA) certified laboratory. * FEV1 greater than or equal to 80% of the predicted value
Exclusion criteria
* Pregnant or intending to become pregnant within 4 years of study entry * Previous lung transplantation * Sibling of a participant who is already enrolled in the study * Unable to attend scheduled clinic visits * Currently smokes cigarettes or marijuana or quit smoking cigarettes or marijuana in the 1 year prior to study entry * Current or planned use of oral tobacco products or nicotine replacement products * Evidence of significant long-term or acute inflammation outside the lung, including connective diseases, panniculitis, or acute infection * Unwilling to alter bronchodilator medications for 24 hours prior to scheduled quantitative CT (QCT) scans * Musculoskeletal disease that limits exercise by walking * Required to take any of the following medications within 48 hours of scheduled lung function testing: dicyclomine (Bentyl), propantheline (Pro-Banthine), mepenzolate (Cantil), methscopolamine (Pamine), and scopolamine (Transderm-Scop) * Known allergy or intolerance to tiotropium or albuterol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CT density slope | 3 years |
Countries
United States
Outcome results
None listed