Medically reviewed by Jerome Albert Ecker | MD, Assistant Professor of Medicine, Duke University - Durham, NC on July 2nd, 2023.
This genetic condition occurs when inherited mutations cause the liver to produce defective AAT protein, which normally protects lung tissue from enzyme damage—affecting roughly 1 in 3,000 people worldwide.
Symptoms typically emerge between ages 20-50, starting with persistent wheezing and shortness of breath during exercise, progressing to chronic cough and frequent respiratory infections as lung damage accumulates.
Diagnosis requires a simple blood test measuring AAT levels (normal is 150-350 mg/dL) plus genetic testing to identify specific mutations like PiZZ, the most severe form causing 10-15% of normal protein levels.
Weekly IV augmentation therapy infuses 60mg/kg of pooled human AAT protein over 15-30 minutes, slowing lung function decline by approximately 40% when started before severe damage occurs.
Avoiding cigarette smoke is critical—smoking accelerates lung deterioration by 2-3 times the normal rate, and even secondhand exposure significantly worsens outcomes in deficient individuals.
Alpha-1 Antitrypsin (AAT) Deficiency is a genetic condition that can lead to serious lung or liver disease. It occurs when your liver doesn't produce enough of the AAT protein, which is essential for protecting your lungs from inflammation and damage caused by infections and irritants like smoke and pollution.
Symptoms of AAT Deficiency often appear between the ages of 20 and 50. If your lungs are affected, you may experience:
Wheezing or whistling sounds when you breathe
Frequent colds
Fatigue
Rapid heartbeat when standing up
Weight loss
If your liver is affected, you may notice:
Yellowing of the skin or eyes (jaundice)
Swelling in the belly or legs
Coughing up blood
To diagnose AAT Deficiency, your doctor may perform several tests, including:
Blood tests to measure AAT levels and liver function
Genetic testing to identify abnormal genes
Imaging tests like X-rays and CT scans to assess lung damage
Pulmonary function tests to measure lung capacity
Liver ultrasound or elastography to check for liver scarring
Liver biopsy to examine cells for damage
While there is no cure for AAT Deficiency, treatment can help protect your lungs from further damage. The most common treatment is augmentation therapy, which involves receiving a new supply of AAT protein from healthy donors through an IV once a week. This can slow or stop lung damage, but it won't reverse any existing damage.
Other treatment options may include:
Bronchodilators to open airways
Supplemental oxygen
Pulmonary rehabilitation to learn breathing techniques and exercises
If your liver is severely damaged, you may need a liver transplant.
To manage your symptoms and maintain your health with AAT Deficiency, it's important to:
Avoid irritants like smoke, dust, and pet hair
Practice good hygiene to prevent infections
Stay up to date on vaccinations
Exercise safely with your doctor's guidance
Eat a healthy diet
Limit alcohol consumption
Avoid smoking
Remember, with proper care and treatment, many people with AAT Deficiency can live a normal lifespan. Work closely with your healthcare team to develop a plan that works for you, and don't hesitate to reach out for support when you need it.
For more information and resources, visit the Alpha-1 Foundation website, the MedlinePlus AAT Deficiency page, or the National Institute of Health's Genetic and Rare Diseases Information Center.
Early detection and treatment with augmentation therapy can dramatically slow lung damage, but the window for maximum benefit closes as scarring progresses. Getting tested is especially important if you have unexplained breathing problems and family history of lung or liver disease. If you're experiencing persistent respiratory symptoms, Doctronic can help connect you with appropriate testing and specialist care.
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