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Alpha-1 Antitrypsin (Serum) Concentration

Published: August 9, 2026Updated: August 16, 2026

This test measures the level of Alpha-1 Antitrypsin, a protein produced by the liver that helps protect the lungs from damage caused by enzymes released during inflammation.

Quick summary

["A1AT levels can help diagnose or monitor conditions affecting the lungs or liver."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
22554-0
Short code
Deprecated S pneum7f Ab sp2 Ser-aCnc
Synonyms
Deprecated S pneum7f Ab sp2 Ser-aCnc
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 healthcare provider may recommend this test if you have symptoms like chronic cough, shortness of breath, or liver issues such as jaundice, fatigue, or abdominal pain. It may also be used to check for genetic conditions like Alpha-1 Antitrypsin Deficiency, which can lead to lung diseases like emphysema or liver diseases over time.

What to Expect During the Test

A blood sample will be taken from a vein in your arm. You may feel a slight pinch, but it usually doesn’t cause discomfort. The sample is then sent to a lab for analysis.

What the Results Mean

Lower than expected levels of Alpha-1 Antitrypsin might indicate a genetic deficiency or liver disease. Higher levels may be seen in certain inflammatory conditions or during pregnancy. Your results will be compared to standard reference ranges provided by your healthcare provider.

Common Conditions Monitored

This test is often used to monitor individuals with a known history of Alpha-1 Antitrypsin Deficiency, chronic obstructive pulmonary disease (COPD), or liver diseases such as cirrhosis.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Alpha-1 Antitrypsin Deficiency is a genetic disorder that can lead to lung diseases like emphysema and liver diseases. Low levels of A1AT can indicate these conditions, prompting further evaluation and management. Regular monitoring of A1AT levels is crucial for patients with known deficiency to prevent complications and guide treatment decisions.

Short name

Alpha-1 Antitrypsin (A1AT)

Frequently asked questions

What does an abnormal A1AT level indicate?
An abnormal A1AT level may suggest a genetic deficiency, liver disease, or other inflammatory conditions. Your healthcare provider will discuss the results in detail and may recommend additional tests or treatments based on your specific situation.
How often should I get this test?
The frequency of testing depends on your medical history and condition. If you have Alpha-1 Antitrypsin Deficiency, your provider may recommend regular monitoring. Otherwise, this test is usually ordered as needed for specific symptoms or concerns.
Can diet or lifestyle changes affect A1AT levels?
While diet and lifestyle factors can influence overall health, they typically do not significantly alter A1AT levels. However, maintaining a healthy lifestyle can support overall well-being, especially if you have a genetic condition like Alpha-1 Antitrypsin Deficiency.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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