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Serum or plasma concentration of alpha-1 antitrypsin (A1AT) measured by immunoassay

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

This test measures the amount of alpha-1 antitrypsin, a protein produced by the liver that helps protect the lungs from damage caused by enzymes released during inflammation or injury.

Quick summary

["Alpha-1 antitripsin helps prevent lung disease and supports immune function; low levels may indicate genetic risk or liver issues."]

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

Key facts at a glance

LOINC
14471-7
Short code
C trach Ag Vag Ql IA
Synonyms
C trach Ag Vag Ql IA
Category
chemistry
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
ia
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 Is This Test Done?

Your healthcare provider may order this test if you have symptoms of lung problems (like chronic bronchitis or emphysema), liver disease, or if you have a family history of alpha-1 antitripsin deficiency. It can also help diagnose or monitor conditions like cirrhosis or certain inflammatory diseases.

What to Expect Before the Test

No special preparation is needed. If you’re having blood drawn, you may feel a slight pinch, but it usually doesn’t cause discomfort. If you’re tested via urine or other fluid, follow any specific instructions your provider gives you.

What the Results Mean

Results are compared to a standard range for healthy individuals. Very low levels may suggest a genetic disorder (like alpha-1 antitripsin deficiency), while very high levels could indicate liver disease or other conditions. Your provider will discuss these findings with you.

Common Conditions Linked to This Test

Low alpha-1 antitripsin levels are most strongly linked to alpha-1 antitripsin deficiency, which can cause lung diseases like emphysema or chronic obstructive pulmonary disease (COPD). It may also be associated with liver diseases like cirrhosis or hepatitis.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Abnormal results can signal an underlying health concern that requires further evaluation, such as genetic testing or additional bloodwork to assess liver or lung function. Always discuss your results with your healthcare provider for personalized guidance.

Short name

Alpha-1 Antitrypsin Level

Frequently asked questions

What causes alpha-1 antitripsin levels to be low?
Low alpha-1 antitripsin levels are most commonly due to a genetic mutation (alpha-1 antitripsin deficiency), but they can also result from liver disease, chronic inflammation, or certain medications.
How long does it take to get results from this test?
Test results are typically available within 1 to 3 business days, depending on your lab and healthcare provider’s workflow. Follow-up appointments may be scheduled if further testing is needed.
Can diet or lifestyle changes affect alpha-1 antitripsin levels?
Diet and lifestyle factors generally do not directly alter alpha-1 antitripsin levels, but managing conditions like liver disease or smoking can indirectly support overall health and may influence related symptoms.
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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