Serum or Plasma Enzyme Activity for Specific Protease Inhibitor (e.g., Alpha-1 Antitrypsin)
This test measures the level of alpha-1 antitrypsin, a protein that helps protect your lungs and liver from damage caused by enzymes released during inflammation or injury.
["Alpha-1 antitrypsin helps prevent lung disease and liver problems by regulating enzymes that break down tissues."]
Key facts at a glance
- LOINC
- 55163-0
- Short code
- S pyog enzyme Ab Pnl Ser
- Synonyms
- S pyog enzyme Ab Pnl Ser
- Category
- coagulation
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
Why This Test Might Be Ordered
Your doctor may recommend this test if you have a family history of lung diseases like emphysema or chronic obstructive pulmonary disease (COPD), liver disease, or if you have symptoms such as persistent coughing, shortness of breath, or unexplained liver issues. It can also be part of screening for genetic conditions affecting this protein.
What to Expect Before the Test
You’ll typically have a simple blood draw from a vein in your arm. No special preparation is usually needed, but your doctor may advise fasting if the test is part of a broader metabolic evaluation. Avoid smoking or strenuous activity for a few hours before the test if it relates to lung health.
What the Results Mean
Low levels of alpha-1 antitrypsin may indicate a genetic deficiency linked to lung or liver disease. High levels might be seen in certain inflammatory conditions or during pregnancy. Your doctor will interpret results in the context of your overall health and symptoms.
Common Conditions Monitored
This test is often used to diagnose or monitor conditions like alpha-1 antitrypsin deficiency, which can lead to emphysema or cirrhosis. It may also help assess liver function or guide treatment plans for chronic inflammatory diseases.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Alpha-1 antitrypsin deficiency is a genetic disorder where the body produces an abnormal form of the protein, leading to its buildup in the lungs or liver. Over time, this can cause irreversible damage, resulting in lung diseases (e.g., emphysema) or liver cirrhosis. Early detection through blood tests can help manage symptoms and slow progression with lifestyle changes or medications.
Short name
Alpha-1 Antitrypsin Activity (Serum/Plasma)
Frequently asked questions
What causes low alpha-1 antitrypsin levels?
How is alpha-1 antitrypsin deficiency diagnosed?
Can lifestyle changes help if I have low alpha-1 antitrypsin?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy