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Alpha-1 Antitrypsin (AAT), Quantitative Test

The Alpha-1 Antitrypsin (AAT) test is a quantitative blood test used to measure the levels of AAT, a protein produced by the liver that protects tissues from damage caused by enzymes like neutrophil elastase. Abnormal levels of AAT can indicate genetic disorders or liver and lung diseases, making this test essential for early diagnosis and management.

What is the AAT Test Used For?

The AAT test helps:

  1. Diagnose Alpha-1 Antitrypsin Deficiency, a genetic disorder leading to lung and liver damage.
  2. Evaluate chronic obstructive pulmonary disease (COPD) when AAT deficiency is suspected.
  3. Investigate unexplained liver disease in infants, children, and adults.
  4. Monitor AAT levels in individuals receiving AAT replacement therapy.

Symptoms Indicating the Need for the Test

The AAT test is recommended if you exhibit:

Shortness of breath or wheezing

Shortness of breath or wheezing

Chronic cough with phlegm

Chronic cough with phlegm

Recurrent respiratory infections

Recurrent respiratory infections

Unexplained liver dysfunction or jaundice

Unexplained liver dysfunction or jaundice

Preparation for the Test

To prepare for the AAT test:

  1. Fasting: No fasting is typically required unless instructed otherwise.
  2. Medication Disclosure: Inform your doctor about any medications, as they may affect AAT levels.

The test involves a simple blood draw from a vein, usually in the arm.

Interpretation of Results

Results are reported in milligrams per deciliter (mg/dL). Normal reference ranges can vary slightly between laboratories but typically include:

  • Normal Range: 100–300 mg/dL.

Abnormal Results:

  • Low AAT Levels:
    • Indicate Alpha-1 Antitrypsin Deficiency.
    • Associated with increased risk of emphysema, chronic bronchitis, or liver disease.
  • High AAT Levels:
    • Can occur due to infections, inflammation, or other acute-phase reactions.

Further testing, such as genetic analysis or liver function tests, may be required to confirm the diagnosis and guide treatment.

FAQs

What is Alpha-1 Antitrypsin Deficiency?

It is a genetic condition where the body produces insufficient or defective AAT, leading to tissue damage, especially in the lungs and liver.

Can lifestyle changes help manage AAT deficiency?

Yes, avoiding smoking, reducing exposure to lung irritants, and maintaining a healthy lifestyle can help reduce symptoms and complications.

How is AAT deficiency treated?

Treatment may include AAT replacement therapy, medications for respiratory symptoms, and in severe cases, liver or lung transplantation.

Can AAT levels fluctuate due to temporary conditions?

Yes, AAT levels may rise during infections, inflammation, or pregnancy, so results must be interpreted in the context of overall health.

Is the test recommended for family members of someone with AAT deficiency?

Yes, family screening is advisable since AAT deficiency is hereditary.

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