Pediatric alpha-1 antitrypsin deficiency (A1AT)

What is pediatric alpha-1 antitrypsin deficiency (A1AT)?

Alpha-1 antitrypsin deficiency (A1AT), also called AATD or Alpha-1, is a rare disorder that can lead to liver and lung disease. It occurs when your child doesn’t have enough of a protein called alpha-1 antitrypsin in their blood. This protein protects the lungs and the liver from infection.

A child with A1AT deficiency can develop liver damage at any age. They may not develop lung disease until adulthood, and it can be made worse by tobacco smoke.

Risk factors

Only about 1 in 3,000 to 1 in 5,000 people in North America have this condition.

What are the signs and symptoms of pediatric alpha-1 antitrypsin deficiency (A1AT)?

• Difficulty breathing
• Chronic cough
• Repeated lung infections
• Cirrhosis (liver disease)
• Emphysema (lung disease)
• Environmental allergies
• Fatigue (extreme tiredness)
• Jaundice
• Liver cancer
• Panniculitis
• Rapid heartbeat
• Shortness of breath
• Wheezing
• Weight loss
• Vomiting blood (due to liver damage)

Not all children with A1AT will show symptoms of the condition.

How is pediatric alpha-1 antitrypsin deficiency (A1AT) diagnosed?

Your child’s doctor may order a blood test to check A1AT levels and genetic phenotype in their blood if they have a family member with the condition.

If your child has low A1AT levels or tests positive with genetic testing, they may need tests including:

• Lung function tests such as spirometry
• A chest X-ray or CT scan of their lungs to check for scarring
• A liver ultrasound to look for liver damage
• A iver biopsy to check for cirrhosis

These tests determine how well your child’s liver and lungs are working.

What causes pediatric alpha-1 antitrypsin deficiency (A1AT)?

A mutation (change) in a gene causes A1AT deficiency. A child must inherit the mutated gene from both parents to get this condition. Parents might not have A1AT deficiency even if their child does.

How is pediatric alpha-1 antitrypsin deficiency (A1AT) treated?

Your child might never have complications from A1AT deficiency. To help reduce their risk of complications, they should:

• Exercise regularly
• Maintain a healthy weight
• Avoid exposure to toxic chemicals in the air
• Avoid alcohol and tobacco smoke, including secondhand smoke

At Children’s Health, our expert pulmonologists and gastroenterologists work together to monitor your child’s health with regular visits.

A treatment plan is personalized for your child and may include:

Augmentation therapy

With this therapy, your child receives donated A1AT through blood infusions every week or month.

Medications such as inhalers

Asthma inhalers and medicines can help your child’s airways open up so they can breathe easier.

Antibiotics

Antibiotics can help prevent or treat lung infections.

Oxygen therapy

Your child may benefit from using an oxygen tank and mask to improve their blood oxygen levels if their lungs aren’t working well.

Pulmonary rehabilitation

Pulmonary rehabilitation can help strengthen your child’s lungs with different breathing exercises.

Liver transplant

It is very rare for a child to need a liver transplant for A1AT deficiency. We are the only children’s hospital in North Texas that offers liver transplants.