Primary Biliary Cholangitis (PBC) is a chronic liver disease characterized by the destruction of small bile ducts in the liver. It primarily affects middle-aged women, with a prevalence estimated to be around 1 in 1,000 to 1 in 4,000 individuals worldwide. PBC is more common in certain regions, such as Northern Europe and North America. Early diagnosis and treatment are crucial to prevent disease progression and complications. Regular monitoring and management by healthcare professionals are recommended for individuals with PBC.
Primary Biliary Cholangitis (PBC) is a chronic autoimmune liver disease that primarily affects middle-aged women. It is characterized by the progressive destruction of small bile ducts within the liver, leading to impaired bile flow and subsequent liver damage. PBC is considered a rare disease, but its prevalence varies across different populations.
According to various studies, the estimated prevalence of PBC ranges from 40 to 400 cases per million individuals. However, it is important to note that these figures may not accurately represent the true prevalence due to underdiagnosis and misdiagnosis of the condition.
PBC is more commonly found in certain regions, such as Northern Europe and North America, compared to other parts of the world. Additionally, the prevalence of PBC tends to increase with age, with the highest rates observed in individuals between 50 and 70 years old.
Early detection and diagnosis of PBC are crucial for initiating appropriate treatment and preventing further liver damage. If you suspect you may have symptoms related to PBC, it is important to consult a healthcare professional for proper evaluation and guidance.