Has contributed equally to the study.
Original Article
IgA antibodies against tissue transglutaminase, endomysium and gliadin in idiopathic polyneuropathy
Article first published online: 1 JUN 2012
DOI: 10.1111/j.1600-0404.2012.01687.x
© 2012 John Wiley & Sons A/S
Additional Information
How to Cite
Vrethem M, Lindh J, Tondel M, Persson B, Dahle C. IgA-antibodies against tissue-transglutaminase, endomysium and gliadin in idiopathic polyneuropathy. Acta Neurol Scand: 2013: 127: 109–115. © 2012 John Wiley & Sons A/S.
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Has contributed equally to the study.
Publication History
- Issue published online: 22 JAN 2013
- Article first published online: 1 JUN 2012
- Manuscript Accepted: 4 MAY 2012
- Abstract
- Article
- References
- Cited By
Keywords:
- neuropathy;
- idiopathic;
- gluten sensitivity;
- coeliac disease;
- anti-tissue transglutaminase;
- anti-gliadin;
- anti-endomysium
Objectives
To study the prevalence of antibodies of IgA class against tissue transglutaminase (tTG), endomysium (EMA) and gliadin (AGA) in patients with chronic idiopathic axonal polyneuropathy (CIAP) and to characterize the patients clinically and neurophysiologically.
Methods
Of 182 patients, 126 patients agreed to blood sampling. Sera were analysed by ELISAs detecting anti-tTG and AGA, whereas EMA was analysed by indirect immunofluorescence (IF) microscopy. Gastrointestinal symptoms were assessed by data from medical records and patient interviews.
Results
Nine of 126 patients (7%) were seropositive in at least one test (five with positive anti-tTG and/or EMA and four with positive AGA only). One patient with elevated levels of all specificities had laboratory signs of malabsorption and gastrointestinal complaints with abdominal pain and diarrhoea.
Conclusions
Elevated levels of IgA-AGA were slightly more frequent in patients with CIAP (4%) compared to 2.5% in 1866 healthy blood donors. Highly specific serological markers indicative of coeliac disease (CD) (anti-tTG and EMA) were somewhat more common in our patients with CIAP (4%) than expected from normal reference values and from studies of the prevalence of CD in the general population. Even though these findings may indicate a relationship, the aetiological importance is unclear.

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