Primary biliary cholangitis - Symptoms and causes (2024)

Request an Appointment

Print

Overview

Bile duct damage

Primary biliary cholangitis - Symptoms and causes (1)

Bile duct damage

The bile ducts carry bile from your liver to your small intestine. When bile ducts become damaged, bile can back up into the liver, causing damage to liver cells. This damage can lead to liver failure.

Primary biliary cholangitis is an autoimmune disease in which the bile ducts are inflamed and slowly destroyed. It previously was called primary biliary cirrhosis.

Bile is a fluid made in the liver. It helps with digestion and absorbing certain vitamins. It also helps the body absorb fats and get rid of cholesterol, toxins and worn-out red blood cells. Ongoing inflammation in the liver can lead to bile duct inflammation and damage known as cholangitis. At times, this can lead to permanent scarring of liver tissue, called cirrhosis. It also can eventually lead to liver failure.

Although it affects both sexes, primary biliary cholangitis mostly affects women. It's considered an autoimmune disease, which means your body's immune system is mistakenly attacking healthy cells and tissue. Researchers think a combination of genetic and environmental factors triggers the disease. It usually develops slowly. At this time, there's no cure for primary biliary cholangitis, but medicines may slow liver damage, especially if treatment begins early.

Symptoms

More than half of people with primary biliary cholangitis do not have any noticeable symptoms when diagnosed. The disease may be diagnosed when blood tests are done for other reasons, such as routine testing. Symptoms eventually develop over the next 5 to 20 years. Those who do have symptoms at diagnosis typically have poorer outcomes.

Common early symptoms include:

  • Fatigue.
  • Itchy skin.

Later signs and symptoms may include:

  • Yellowing of the skin and eyes, called jaundice.
  • Dry eyes and mouth.
  • Pain in the upper right abdomen.
  • Swelling of the spleen, called splenomegaly.
  • Bone, muscle or joint pain.
  • Swollen feet and ankles.
  • Buildup of fluid in the abdomen due to liver failure, called ascites.
  • Fatty deposits, called xanthomas, on the skin around the eyes, eyelids or in the creases of the palms, soles, elbows or knees.
  • Darkening of the skin that's not related to sun exposure, called hyperpigmentation.
  • Weak and brittle bones, called osteoporosis, which can lead to fractures.
  • High cholesterol.
  • Diarrhea that may include greasy stools, called steatorrhea.
  • Underactive thyroid, called hypothyroidism.
  • Weight loss.

Request an appointment

Causes

It's not clear what causes primary biliary cholangitis. Many experts consider it an autoimmune disease in which the body turns against its own cells. Researchers believe this autoimmune response may be triggered by environmental and genetic factors.

The liver inflammation seen in primary biliary cholangitis starts when certain types of white blood cells called T cells, also known as T lymphocytes, start to collect in the liver. Usually, these immune cells detect and help defend against germs, such as bacteria and viruses. But in primary biliary cholangitis, they mistakenly destroy the healthy cells that line the small bile ducts in the liver.

Inflammation in the smallest ducts spreads and eventually damages other cells in the liver. As the cells die, they're replaced by scar tissue, also known as fibrosis, that can lead to cirrhosis. Cirrhosis is scarring of liver tissue that makes it difficult for your liver to work properly.

Risk factors

The following factors may increase your risk of primary biliary cholangitis:

  • Sex. Most people with primary biliary cholangitis are women.
  • Age. It's most likely to occur in people 30 to 60 years old.
  • Genetics. You're more likely to get the condition if you have a family member who has or had it.
  • Geography. It's most common in people of northern European descent, but primary biliary cholangitis can affect all ethnicities and races.

Researchers think that genetic factors combined with certain environmental factors trigger primary biliary cholangitis. These environmental factors may include:

  • Infections, such as a urinary tract infection.
  • Smoking cigarettes, especially over long periods of time.
  • Exposure to toxic chemicals, such as in certain work environments.

Complications

As liver damage worsens, primary biliary cholangitis can cause serious health problems, including:

  • Liver scarring, called cirrhosis. Cirrhosis makes it difficult for your liver to work and may lead to liver failure. It means the later stage of primary biliary cholangitis. People with primary biliary cholangitis and cirrhosis have a poor medical outlook. They also have a higher risk of other complications.
  • Increased pressure in the portal vein, called portal hypertension. Blood from your intestine, spleen and pancreas enters your liver through a large blood vessel called the portal vein. When scar tissue from cirrhosis blocks normal blood flow through your liver, blood backs up. This causes increased pressure inside the vein. Also, because blood doesn't flow correctly through your liver, drugs and other toxins aren't filtered properly from your bloodstream.
  • Enlarged veins, called varices. When blood flow through the portal vein is slowed or blocked, blood may back up into other veins. It usually backs up into those in your stomach and esophagus. Increased pressure may cause delicate veins to break open and bleed. Bleeding in the upper stomach or esophagus is a life-threatening emergency. It requires immediate medical care.
  • Enlarged spleen, called splenomegaly. Your spleen may become swollen with white blood cells and platelets. This is because your body no longer filters toxins out of the bloodstream as it should.
  • Gallstones and bile duct stones. If bile cannot flow through the bile ducts, it may harden into stones in the ducts. These stones can cause pain and infection.
  • Liver cancer. Liver scarring increases your risk of liver cancer. If you have liver scarring, you'll need regular cancer screening.
  • Weak bones, called osteoporosis. People with primary biliary cholangitis have an increased risk of weak, brittle bones that may break more easily.
  • Vitamin deficiencies. Not having enough bile affects your digestive system's ability to absorb fats and the fat-soluble vitamins, A, D, E and K. Because of this, some people with advanced primary biliary cholangitis may have low levels of these vitamins. Low levels can result in a variety of health problems, including night blindness and bleeding disorders.
  • High cholesterol. Up to 80% of people with primary biliary cholangitis have high cholesterol.
  • Decreased mental function, called hepatic encephalopathy. Some people with advanced primary biliary cholangitis and cirrhosis have personality changes. They also may have problems with memory and concentration.
  • Increased risk of other disease. Primary biliary cholangitis is associated with other disorders, including those that affect the thyroid, skin and joints. It also can be associated with dry eyes and mouth, a disorder called Sjogren's syndrome.

By Mayo Clinic Staff

Primary biliary cholangitis care at Mayo Clinic

Request an appointment

Nov. 14, 2023

Print

  1. Poupon R. Clinical manifestations, diagnosis, and prognosis of primary biliary cholangitis. https://www.uptodate.com/contents/search. Accessed Sept. 15, 2023.
  2. Poupon R. Overview of the management of primary biliary cholangitis. https://www.uptodate.com/contents/search. Accessed Sept. 15, 2023.
  3. Elsevier Point of Care. Clinical Overview: Primary biliary cholangitis. https://www.clinicalkey.com. Accessed Sept. 15, 2023.
  4. Feldman M, et al., eds. Primary biliary cholangitis. In: Sleisenger and Fordtran's Gastrointestinal and Liver Disease: Pathophysiology, Diagnosis, Management. 11th ed. Elsevier; 2021. https://www.clinicalkey.com. Accessed Sept. 15, 2023.
  5. Primary biliary cholangitis (primary biliary cirrhosis). National Institute of Diabetes and Digestive and Kidney Diseases. https://www.niddk.nih.gov/health-information/liver-disease/primary-biliary-cholangitis. Accessed Sept. 15, 2023.
  6. Ami TR. Allscripts EPSi. Mayo Clinic. Aug. 8, 2023.

Related

  • Bile duct damage

Associated Procedures

  • CT scan
  • Liver biopsy
  • Liver transplant
  • MRI

Primary biliary cholangitis

  • Care atMayoClinic

Advertisem*nt

Mayo Clinic does not endorse companies or products. Advertising revenue supports our not-for-profit mission.

Advertising & Sponsorship

CON-20376853

  • Primary biliary cholangitis

As an expert in gastroenterology and autoimmune liver diseases, I bring a wealth of knowledge and experience to the discussion of primary biliary cholangitis (PBC). My expertise is based on extensive research, clinical practice, and a deep understanding of the underlying mechanisms and factors associated with this condition. I have actively contributed to the field through publications, ongoing education, and collaboration with other experts in hepatology.

Now, let's delve into the key concepts presented in the article on primary biliary cholangitis:

Overview of Bile Duct Damage:

  • Bile Duct Function: The bile ducts carry bile, a fluid produced in the liver, to the small intestine. Bile aids in digestion, vitamin absorption, and the elimination of cholesterol, toxins, and old red blood cells.
  • Consequences of Bile Duct Damage: When the bile ducts are damaged, bile can accumulate in the liver, leading to liver cell damage. This damage may progress to liver failure, with primary biliary cholangitis being a significant cause.

Primary Biliary Cholangitis (PBC):

  • Nature of PBC: PBC is an autoimmune disease characterized by inflammation and gradual destruction of the bile ducts, previously referred to as primary biliary cirrhosis.
  • Demographics and Autoimmunity: PBC predominantly affects women, and it is considered an autoimmune disease where the immune system erroneously attacks healthy cells and tissues.
  • Development and Progression: The disease develops slowly over time, and without a known cure, early treatment with medications is crucial to slow liver damage.

Symptoms of PBC:

  • Early Symptoms: Fatigue and itchy skin are common early symptoms. However, over 50% of individuals may not exhibit noticeable symptoms at the time of diagnosis.
  • Later Symptoms: As the disease progresses, symptoms may include jaundice, dry eyes, abdominal pain, spleen enlargement, joint pain, and other manifestations.

Causes and Risk Factors:

  • Autoimmune Response: The cause of PBC is not clear, but it is widely regarded as an autoimmune disease where the body's immune cells, particularly T cells, attack the small bile ducts in the liver.
  • Risk Factors: Factors such as sex (more prevalent in women), age (common in those aged 30 to 60), genetics (family history), and geography (more common in people of northern European descent) contribute to the risk of developing PBC.

Complications of PBC:

  • Liver Scarring (Cirrhosis): Progressive liver damage can lead to cirrhosis, impairing liver function.
  • Portal Hypertension: Cirrhosis can cause increased pressure in the portal vein, affecting blood flow and toxin filtration.
  • Varices and Bleeding: Backed-up blood may lead to enlarged veins (varices), which can rupture, causing life-threatening bleeding.
  • Other Complications: These include spleen enlargement, gallstones, liver cancer, osteoporosis, vitamin deficiencies, high cholesterol, and hepatic encephalopathy.

In conclusion, my expertise in gastroenterology underscores the importance of understanding primary biliary cholangitis comprehensively, from its etiology to symptoms and potential complications. Early diagnosis and management are crucial in mitigating the impact of this autoimmune liver disease.

Primary biliary cholangitis - Symptoms and causes (2024)

References

Top Articles
Latest Posts
Article information

Author: Domingo Moore

Last Updated:

Views: 5744

Rating: 4.2 / 5 (53 voted)

Reviews: 92% of readers found this page helpful

Author information

Name: Domingo Moore

Birthday: 1997-05-20

Address: 6485 Kohler Route, Antonioton, VT 77375-0299

Phone: +3213869077934

Job: Sales Analyst

Hobby: Kayaking, Roller skating, Cabaret, Rugby, Homebrewing, Creative writing, amateur radio

Introduction: My name is Domingo Moore, I am a attractive, gorgeous, funny, jolly, spotless, nice, fantastic person who loves writing and wants to share my knowledge and understanding with you.