Abstract |
In primary biliary cirrhosis, autoantibodies are produced to the family of 2-oxoacid dehydrogenase complexes. These 'anti-mitochondrial' antibodies are traditionally detected by immunofluorescence but this method of detection is subjective and labour-intensive. We assessed an enzymatic mitochondrial antibody (EMA) assay based on antibody inhibition of enzymatic activity of pyruvate dehydrogenase complex in wells of microtitre plates with a colorimetric read-out. We tested 48 Australian and 1947 Japanese patients with primary biliary cirrhosis, 306 normal subjects and 691 patients with various hepatic and non-hepatic diseases. The overall sensitivity of the EMA for the diagnosis of primary biliary cirrhosis, 82%, was slightly lower than that of immunofluorescence, 90% The advantages of the EMA test include high specificity, >99%, and semi-automated features facilitating objectivity, rapidity, simplicity and economy. The EMA test could be particularly applicable to population screening for early primary biliary cirrhosis.
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Authors | J Jois, K Omagari, M J Rowley, J Anderson, I R Mackay |
Journal | Annals of clinical biochemistry
(Ann Clin Biochem)
Vol. 37 ( Pt 1)
Pg. 67-73
(Jan 2000)
ISSN: 0004-5632 [Print] England |
PMID | 10672375
(Publication Type: Journal Article)
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Chemical References |
- Autoantibodies
- Enzyme Inhibitors
- Pyruvate Dehydrogenase Complex
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Topics |
- Autoantibodies
(analysis, immunology)
- Enzyme Inhibitors
(immunology)
- Enzyme-Linked Immunosorbent Assay
- Female
- Humans
- Liver Cirrhosis, Biliary
(diagnosis, immunology)
- Male
- Predictive Value of Tests
- Pyruvate Dehydrogenase Complex
(antagonists & inhibitors, immunology)
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