This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Aetiology

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

PBC is considered to be the model autoimmune disease where a variety of environmental toxins or infectious agents may trigger an immune response on a genetically susceptible individual (1).

A combination of multiple genetic factors and environmental factors affect the immune system and the liver

  • genetic factors/susceptibility
    • the impact of genetic factors on PBC pathogenesis is stronger than that in nearly any other autoimmune disease
    • 1-6% of individuals with PBC have at least one family member manifesting disease
    • a concordance rate of 63% in identical twins is amongst the highest of all autoimmune diseases
    • the role of susceptibility genes in PBC is yet to be identified

  • environmental factors
    • infectious and chemicals are thought to trigger PBC largely through molecular mimicry or modification of autoantigens
    • examples for infections
      • Novosphingobium aromaticivorans
      • Escherichia coli
      • Helicobacter spp.
    • examples for chemicals
      • foreign chemicals like xenobiotics (1)

Reference:


Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.