What Is Alpha-1 Antitrypsin Deficiency?
Alpha-1 antitrypsin (an-tee-TRIP-sin) deficiency, or
AAT deficiency, is a condition that raises your risk for certain types of lung
disease, especially if you smoke. AAT deficiency is an inherited condition.
"Inherited" means it's passed in the genes from parents to children.
Some people who have severe AAT deficiency develop
emphysema (em-fi-SE-ma)often when they're only in their
forties or fifties. Emphysema is a serious lung disease in which damage to the
airways makes it hard to breathe.
A smaller number of people who have AAT deficiency
have
cirrhosis (sir-RO-sis) and other serious liver diseases.
Cirrhosis is a disease in which the liver is
scarred. This prevents the liver from working properly. In people who have AAT
deficiency, cirrhosis and other liver diseases usually occur in infancy and
early childhood.
A very small number of people who have AAT
deficiency have a rare type of skin disease called necrotizing panniculitis
(pa-NIK-yu-LI-tis). This skin disease can cause painful lumps under or on the
surface of the skin.
This article will focus on AAT deficiency as it
relates to lung disease.
Overview
Alpha-1 antitrypsin, also called AAT, is a protein
made in the liver. Normally, the protein goes into the bloodstream and helps
protect the body's organs from the harmful effects of other proteins. One of
the main organs it protects is the lungs.
AAT deficiency occurs when the AAT proteins made in
the liver aren't the right shape. They get stuck inside liver cells and can't
get into the bloodstream. Because not enough AAT protein travels to the lungs
to protect them, the risk of lung disease increases. Also, because too many AAT
proteins are stuck in the liver, liver disease can develop.
AAT deficiency is considered severe when blood
levels of the AAT protein fall below the lowest amount needed to protect the
lungs.
AAT deficiency is an inherited condition caused by
altered genes. It's not known how many people have it. Many people who have it
may not know they have it. Estimates of how many people have the condition
range from about 1 in every 1,600 people to about 1 in every 5,000 people.
Outlook
You may not have any serious complications if you
have AAT deficiency, and you may live a normal lifespan. Many nonsmokers who
have AAT deficiency don't develop any serious related lung diseases.
Among people with AAT deficiency who do have a
related lung or liver disease, about 3 percent die each year. Smoking is the
leading risk factor for life-threatening lung disease if you have AAT
deficiency. If you have severe AAT deficiency, smoking can shorten your life by
as much as 20 years.
AAT deficiency has no cure, but there are
treatments. In most cases, treatment is based on the type of disease you
develop.
November 2007
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