Exp Clin Endocrinol Diabetes 2007; 115(6): 387-391
DOI: 10.1055/s-2007-967082
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG · Stuttgart · New York

Impaired Deoxyribonuclease Activity in Monoglandular and Polyglandular Autoimmunity

M. Dittmar 1 , 2 , R. Poppe 3 , C. Bischofs 1 , G. Fredenhagen 3 , M. Kanitz 1 , G. J. Kahaly 1
  • 1Department of Medicine I, Gutenberg University, Mainz, Germany
  • 2Department of Biology, Gutenberg University, Mainz, Germany
  • 3ORGENTEC Diagnostics, Germany
Further Information

Publication History

received 11. 09. 2006 first decision 10. 01. 2007

accepted 10. 01. 2007

Publication Date:
08 June 2007 (online)

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Abstract

Objective: The enzyme desoxyribonuclease (DNase) degrades DNA during early apoptosis. Impaired DNase activity might increase susceptibility to autoimmune diseases. This study examined for the first time DNase activity in endocrine autoimmunity.

Methods: Included were 112 patients with monoglandular (MGA) or polyglandular autoimmunity (PGA), their 93 healthy relatives, and 41 healthy controls. Serum DNase activity was quantified with a solid phase enzyme immunometric assay comprising degradation of the specific immobilized DNase substrate, formation of enzyme conjugate complexes using horseradish peroxidase conjugate solution, and enzymatic colour reaction.

Results: The Bland-Altman plot of the interassay differences suggested good reproducibility (n=96). Compared to healthy controls (median 9.8, range 5.2-16.7 ng/ml), DNase activity was markedly lowered in patients with endocrine autoimmunity (5.8, 2.6-26.2 ng/ml; p<0.0001). Corresponding values in the following MGA, PGA, and relatives groups were 4.8 (2.8-19.0) ng/ml, 7.9 (2.6-26.2) ng/ml, and 8.4 (1.5-19.0) ng/ml, respectively. When MGA patients were splitted up by disease, patients with type 1 diabetes had the lowest DNase activity (3.6, 3.2-3.9 ng/ml) which positively correlated with HbA1c in females (r=0.486, p=0.041). Pathological reduction of DNase activity (below 5 ng/ml) was noted in 54%, 31%, 24%, and 0% of MGA, PGA, relatives, and controls, respectively. Anti-ds-DNA and anti-nucleosome antibodies were negative in the patients with MGA and PGA.

Conclusions: These findings indicate the potential relevance of DNase activity in patients with monoglandular and polyglandular autoimmunity and their clinically healthy relatives. The impaired DNase activity might reduce removal of circulating self- or pathogen-derived DNA thereby favoring autoimmune mechanisms by Toll-like receptor 9 co-activation.

References

Correspondence

G. J. Kahaly

Dept. of Medicine I

Gutenberg University Hospital

Mainz 55101

Germany

Phone: +49/61/31 17 69 50

Fax: +49/61/31 17 34 60

Email: gkahaly@mail.uni-mainz.de