Abstract

Background

IgG-class autoantibodies to N-Methyl-D-Aspartate (NMDA)-type glutamate receptors define a novel entity of autoimmune encephalitis. Studies examining the prevalence of NMDA IgA/IgM antibodies in patients with Parkinson disease with/without dementia produced conflicting results. We measured NMDA antibodies in a large, well phenotyped sample of Parkinson patients without and with cognitive impairment (n = 296) and controls (n = 295) free of neuropsychiatric disease. Detailed phenotyping and large numbers allowed statistically meaningful correlation of antibody status with diagnostic subgroups as well as quantitative indicators of disease severity and cognitive impairment.

Methods

NMDA antibodies were analysed in the serum of patients and controls using well established validated assays. We used anti-NMDA antibody positivity as the main independent variable and correlated it with disease status and phenotypic characteristics.

Results

The frequency of NMDA IgA/IgM antibodies was lower in Parkinson patients (13%) than in controls (22%) and higher than in previous studies in both groups. NMDA IgA/IgM antibodies were neither significantly associated with diagnostic subclasses of Parkinson disease according to cognitive impairment, nor with quantitative indicators of disease severity and cognitive impairment. A positive NMDA antibody status was positively correlated with age in controls but not in Parkinson patients.

Conclusion

It is unlikely albeit not impossible that NMDA antibodies play a significant role in the pathogenesis or progression of Parkinson disease e.g. to Parkinson disease with dementia, while NMDA IgG antibodies define a separate disease of its own.

Details

Title
No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors
Author
Hopfner, Franziska; Müller, Stefanie H; Steppat, Dagmar; Miller, Joanna; Schmidt, Nele; Klaus-Peter Wandinger; Leypoldt, Frank; Berg, Daniela; Franke, Andre; Lieb, Wolfgang; Tittmann, Lukas; Balzer-Geldsetzer, Monika; Baudrexel, Simon; Dodel, Richard; Hilker-Roggendorf, Ruediger; Kalbe, Elke
Publication year
2019
Publication date
2019
Publisher
BioMed Central
e-ISSN
20479158
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2211418922
Copyright
© 2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.