COPD and Alpha-1 Antitrypsin (AAT) Deficiency
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Alpha-1 antitrypsin (AAT) is a protein normally found in
the lungs and the bloodstream. It helps protect the lungs from the damage
caused by inflammation that can lead to
emphysema and
chronic obstructive pulmonary disease (COPD). People
whose bodies do not produce enough of this protein (AAT deficiency) are more
likely to develop emphysema and to do so at a younger-than-normal age (30 to 40
years old). AAT deficiency is a rare disorder and is the only known
genetic (inherited) factor that increases your risk of
developing COPD.
Your doctor may suspect you have an AAT
deficiency if you:footnote 1
- Develop emphysema at 45 years of age or
younger.
- Develop emphysema without having any recognized risk
factors, such as smoking or inhaling industrial dust or chemical fumes over a
long period of time.
- Develop emphysema, and X-rays show less
density in the lungs than normal (basilar hyperlucency).
- Develop
unexplained liver disease.
- Have a family history of emphysema,
bronchiectasis, liver disease, or inflammation of the
fat under the skin (necrotizing panniculitis).
- Have bronchiectasis
without an evident cause.
An AAT deficiency test measures the level of AAT in the
blood. The test is not routinely done in most people with COPD. But the
American Thoracic Society and the European Respiratory Society recommend
testing for an AAT deficiency for people who have:footnote 1
- Symptoms of COPD and have been diagnosed with
emphysema or COPD.
- Asthma with airflow blockage that is
not completely resolved after treatment with medicine that opens the lung
airways (bronchodilators).
- Unexplained liver
disease.
- No symptoms, but lung tests show obstruction, and risk
factors such as smoking are present.
- Necrotizing
panniculitis.
- A brother or sister who is AAT-deficient.
Screening for an AAT deficiency in the general public is not
currently recommended.footnote 1
Treatment
It is extremely important that you do not
smoke if you have an AAT deficiency. Smokers with this condition may suffer
devastating disease at a young age. People with this condition who have never
smoked usually do not have significant symptoms at any age.
Treatment for COPD may include medicines to help you breathe easier. It may also include pulmonary rehabilitation. This means learning exercise, eating, and breathing tips and other ways to help yourself stay as healthy and strong as you can. And your doctor may suggest that you have injections of man-made
alpha-1 antitrypsin protein (also called an alpha-1 proteinase inhibitor) that
has been obtained from human
plasma. Examples include Aralast, Prolastin, and
Zemaira. To be considered for this treatment, you must meet the following
guidelines:
- Your blood levels of the alpha-1 antitrypsin
enzyme are less than 11 µmol/L (micromoles per liter).
- DNA testing
shows that your body does not produce enough of the enzyme or produces an
enzyme that does not work properly.
- You do not smoke or have
stopped smoking.
- You have difficulty breathing because of COPD or
emphysema.
Injections of replacement alpha-1 antitrypsin are given
either weekly or every 2 to 4 weeks. Benefits of the therapy are not clear at
this time.
References
Citations
- American Thoracic Society/European Respiratory Society (2003). ATS/ERS: Standards for the diagnosis and management of individuals with alpha1-antitrypsin deficiency. American Journal of Respiratory and Critical Care Medicine, 168(7): 820-822.
Credits
ByHealthwise Staff
Primary Medical ReviewerE. Gregory Thompson, MD - Internal Medicine
Adam Husney, MD - Family Medicine
Specialist Medical ReviewerKen Y. Yoneda, MD - Pulmonology
Current as ofMarch 25, 2017
Current as of:
March 25, 2017
American Thoracic Society/European Respiratory Society (2003). ATS/ERS: Standards for the diagnosis and management of individuals with alpha1-antitrypsin deficiency. American Journal of Respiratory and Critical Care Medicine, 168(7): 820-822.