AQP4 autoantibodies in patients with idiopathic normal pressure hydrocephalus
Idiopathic normal pressure hydrocephalus (iNPH) is a common neurological disorder with unknown etiology. A selective depletion of aquaporin 4 (AQP4) has been shown in iNPH patients. We collected serum and cerebrospinal fluid (CSF) from 43 iNPH patients and 35 with other neurodegenerative conditions,...
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| Main Authors: | , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
30 September 2020
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| In: |
Journal of neuroimmunology
Year: 2020, Volume: 349 |
| ISSN: | 1872-8421 |
| DOI: | 10.1016/j.jneuroim.2020.577407 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.jneuroim.2020.577407 Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S0165572820305269 
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| Author Notes: | Matteo Gastaldi, Massimiliano Todisco, Giorgia Carlin, Silvia Scaranzin, Elisabetta Zardini, Brigida Minafra, Roberta Zangaglia, Anna Pichiecchio, Markus Reindl, Sven Jarius, Claudio Pacchetti, Diego Franciotta |
| Summary: | Idiopathic normal pressure hydrocephalus (iNPH) is a common neurological disorder with unknown etiology. A selective depletion of aquaporin 4 (AQP4) has been shown in iNPH patients. We collected serum and cerebrospinal fluid (CSF) from 43 iNPH patients and 35 with other neurodegenerative conditions, and serum from 43 healthy subjects. All samples were tested for AQP4-IgG/IgA/IgM antibodies using a live cell-based assay. No patients or controls had serum/CSF AQP4-IgG/IgA. One/43 iNPH patient and 0/43 controls tested positive for serum AQP4-IgM. The AQP4-IgM-positive iNPH patient had no clinico-radiological distinctive features. AQP4 antibodies are unlikely to play a role in iNPH pathogenesis. |
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| Item Description: | Gesehen am 04.01.2021 |
| Physical Description: | Online Resource |
| ISSN: | 1872-8421 |
| DOI: | 10.1016/j.jneuroim.2020.577407 |