On This Page
The principal roles of the liver include removal of toxins from the blood and processing food nutrients into proteins, fats and carbohydrates. The liver produces bile, which is stored in the gall bladder and added to the digestive tract via bile ducts to help break down dietary fats. Primary biliary cholangitis (PBC) is an autoimmune condition characterised by chronic inflammation and subsequent scarring of the bile ducts within the liver.
The cause is unknown, although researchers have ruled out alcohol and diet as possible triggers. Women are 10 times more likely to develop PBC than men, for reasons unknown. The disease is usually diagnosed later in life, between the ages of 35 and 60 years.
There is no cure, but treatment can slow the progression of the disease and alleviate symptoms. PBC is associated with other autoimmune diseases, including rheumatoid arthritis, scleroderma and Sjogren’s syndrome. Symptoms of PBC vary from one person to another, ranging from non-existent to mild to severe.
The symptoms tend to be progressive and can include:
- osteoporosis. Bile drains into the digestive tract via bile ducts. For reasons unknown
- the immune system attacks the cells that line the bile ducts inside the liver
This causes chronic inflammation, damage and scarring
Over time, accumulated scar tissue blocks the ducts and causes a build-up of bile within the liver, which in turn becomes inflamed. Functioning liver tissue is gradually replaced with non-functioning scar tissue (cirrhosis). Eventually, so much of the liver is replaced by scar tissue that it can no longer function properly.
Fortunately, mose people with PBC don’t ever experience this degree of cirrhosis.
As a result, this disorder is now called primary biliary cholangitis, which refers to inflammation of the bile ducts. The older term ‘primary biliary cirrhosis’ is no longer recommended.
PBC is an autoimmune disorder. The immune system attacks the bile ducts, but the trigger for this attack is so far unidentified. Alcohol and diet are not thought to play significant roles in the development of the disease.
PBC seems to be slightly more common in families, which suggests a genetic susceptibility. For reasons unknown, the disease seems to be more common in Scotland, Scandinavia and North East England. By the time symptoms of PBC become apparent, the bile ducts have sustained significant damage.
Early stage PBC is sometimes diagnosed during blood tests and other investigations for unrelated medical conditions. Specific tests for PBC include:
liver biopsy. There is no cure for PBC
but treatment can help slow the progression of disease
associated symptoms
particularly ursodeoxycholic acid (Ursofalk) – for patients who do not respond
obeticholic acid (not available yet in United States)
fibrates can be considered regular weight bearing exercise (such as walking or weight training)
calcium or vitamin D supplementation to reduce the risk of osteoporosis liver transplant
in severe cases
Chronically itchy skin is a maddening symptom of PBC. Some people may even develop scars from constant scratching.
Medications such as cholestyramine and rifampicin can reduce the itchiness. Other suggestions include: Keep fingernails short.
Wear natural fibres like cotton rather than synthetics
Moderate sun exposure may help
Avoid overheating and hot baths
Avoid perfumes, scented soaps, bath oils, bubble bath and talcum powder. Take a cool bath infused with one cup of bicarbonate of soda before bed. About primary biliary cholangitis Symptoms of primary biliary cholangitis increasing fatigue unexplained pigmentation of the skin jaundice (yellowing of the skin and eyes) chronically itchy skin unexplained weight loss indigestion easy bruising aching joints abdominal discomfort around the liver (upper right-hand side of the abdomen) bloated abdomen due to fluid build-up (ascites) swollen feet Destruction of bile ducts Cause of PBC Diagnosis of PBC blood tests liver function tests x-rays ultrasound scans Treatment for PBC fat-soluble vitamin supplements, since absorption of these vitamins from food is reduced low-salt diet diuretics to help control fluid retention medication to treat the itching, such as cholestyramine and rifampicin reduced intake of alcohol and non-essential medications nutritious diet high in vitamins, minerals and trace elements Reducing skin itching Where to get help Your GP (doctor) Gastroenterologist American Primary Biliary Cirrhosis Support Group .
Key Points
- cause is unknown, although researchers have ruled out alcohol and diet as possible triggers
- There is no cure, but treatment can slow the progression of the disease and alleviate symptoms
- Symptoms of PBC vary from one person to another, ranging from non-existent to mild to severe
- symptoms tend to be progressive and can include: osteoporosis
- This causes chronic inflammation, damage and scarring