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Chinese Journal of Clinical Laboratory Management(Electronic Edition) ›› 2017, Vol. 05 ›› Issue (04): 197-199. doi: 10.3877/cma.j.issn.2095-5820.2017.04.002

Special Issue:

• Expert Opinion • Previous Articles     Next Articles

Laboratory diagnosis of primary biliary cholangitis

Chunxia Wang1,(), Jiajia Wang1   

  1. 1. Autoimmune Disease Diagnostic Center, Jinan Kingmed Diagonostics, Jinan 250101, China
  • Received:2017-09-17 Online:2017-11-28 Published:2017-11-28
  • Contact: Chunxia Wang
  • About author:
    Corresponding author: Wang Chunxia, Email:

Abstract:

Primary biliary cholangitis (PBC) is the most common disease among autoimmune liver diseases. PBC is a chronic cholestatic disease with a progressive course which may extend over many decades. The disease offten has insidious onset and is quite often misdiagnosed or results in a prolonged course. Antimitochondrial autoantibodies (AMA) are the classical specific serological marker of PBC and are found in 90% to 95% of PBC patients. Antibodies to glycoprotein 210 (gp210) and nuclear autoantigen Sp 100 (sp100) are specific for PBC but with low sensitivity. They are more useful for dignosising AMA-negative PBC. An association between anti-gp210 antibodies and disease severity has been reported. AMA may be detectable in serum when patients are symptom-free and liver function tests are normal. Screening the patients during the early stage of the disease process, can influence the clinical phenotype, and long-term prognosis of PBC, and improve the quality of patient′s life.

Key words: Autoimmune liver diseases, Primary biliary cholangitis, Antimitochondrial autoantibody

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