Primary biliary cholangitis is a type of liver disease that damages the bile ducts. Early recognition and treatment may help prevent complications.
Update Date: 27.02.2026
Primary biliary cholangitis (PBC) is an uncommon, long-term disease of the liver in which the body's immune system mistakenly attacks bile ducts within the liver. This gradually decreases the flow of bile from the liver to the small intestine. A buildup of bile damages and destroys liver tissues.
Primary biliary (BIL-ee-air-ee) cholangitis (koh-lan-JIE-tis) destroys the lining of the small- and medium-sized bile ducts that transport the digestive fluid bile from the liver. Leaking bile and related disease activity damage liver tissues. If left untreated, PBC can lead to scarring of tissues in the liver and liver failure. PBC most often affects middle-aged and older women.
Treatments for PBC include medicines to delay progression of the disease and to treat symptoms such as itching, extreme tiredness, and dry eyes and mouth. Advanced disease may require a liver transplant.
PBC was formerly called primary biliary cirrhosis.
More than 50% of people with primary biliary cholangitis do not have symptoms when they get a diagnosis. But symptoms appear at some point as damage to the liver worsens.
Symptoms often include:
Other signs and symptoms may include:
Make an appointment with your healthcare professional if you have severe, persistent itching on much of your body with no obvious cause. Also, see your health professional if you feel extremely tired all the time, no matter how much rest you get.
Primary biliary cholangitis (PBC) is an autoimmune disease. This means the body's immune system attacks its own tissues as if it were fighting a disease.
Usually, certain types of white blood cells, called lymphocytes, find and attack germs or other foreign substances. In PBC, lymphocytes mistakenly target healthy cells lining the small- and medium-sized bile ducts in the liver. The immune system also makes disease-fighting proteins, called antibodies, that attack these healthy cells.
Bile ducts in the liver are gradually damaged and destroyed, causing bile to build up in the liver. This buildup is called cholestasis.
Leaking bile, inflammation and other immune system activity causes damage and scarring of liver tissues. This scarring, called fibrosis, leads to poor liver function. Eventually, fibrosis can lead to severe, permanent scarring, called cirrhosis.
It's not clear what triggers this autoimmune disease. Research suggests several potential triggers that may lead to PBC in people with a genetic risk of the disease. These triggers may include:
People with PBC often have another autoimmune disease. These may include:
The following factors may increase your risk of primary biliary cholangitis:
As liver damage worsens, primary biliary cholangitis (PBC) can cause serious health problems, including:
Your healthcare professional performs a physical exam and asks you about your health history.
The following tests and procedures are the primary means for making a diagnosis of primary biliary cholangitis (PBC).
Imaging tests are usually not necessary to make a diagnosis. But they may be used to rule out other diseases or understand the condition of the liver. Imaging tests include:
A test for cholesterol levels in the blood is common because cholesterol is often high in people with PBC.
Medicines may slow the progression of the primary biliary cholangitis (PBC) and prevent complications. Options include:
A liver transplant is the only treatment known to cure PBC. During a liver transplant, surgeons remove a diseased liver and replace it with a healthy liver from a donor.
A liver transplant is reserved for people with liver failure or other severe complications of PBC. The disease may appear again after a liver transplant.
Your healthcare professional may recommend treatments to control the signs and symptoms of PBC and make you more comfortable.
Artificial tears and saliva substitutes can help ease dry eyes and mouth. These are available with or without a prescription. You can make more saliva and relieve dry mouth by chewing sugarless gum, sucking on sugarless hard candy or eating dried fruit slices.
Certain complications are commonly linked to PBC. Your healthcare professional may recommend:
You may feel better if you take good care of your overall health. Here are some things you can do to improve some primary biliary cholangitis (PBC) symptoms and help prevent certain complications:
Living with liver disease with no cure can be frustrating. Fatigue alone can have a profound impact on your quality of life. Each person finds ways to cope with the stress of a long-term disease. In time, you'll find what works for you. Here are some ways to get started:
If you have signs or symptoms that worry you, make an appointment with your healthcare professional. If you're diagnosed with primary biliary cholangitis, you may be referred to a specialist in diseases of the digestive system, called a gastroenterologist, or a specialist in liver diseases, called a hepatologist.
Because there's often a lot to cover during your appointment, it's a good idea to arrive well prepared.
Preparing a list of questions can help you make the most of your time with your healthcare professional. Questions you may ask at your first appointment or follow-up care appointments may include:
In addition to the questions that you've prepared to ask your healthcare professional, don't hesitate to ask other questions that come to mind during your appointment.
Your healthcare professional is likely to ask you a number of questions. Being ready to answer them may give you more time to discuss a concern in greater detail. Your health professional may ask:
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