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Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis
INTRODUCTION: Neuronal antibodies can cause encephalopathy syndromes often presenting with subacute cognitive impairment, sometimes resembling neurodegenerative dementias. METHODS: We searched Medline and Embase for studies reporting associations between neuronal surface antibodies in all-cause deme...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289796/ https://www.ncbi.nlm.nih.gov/pubmed/32306172 http://dx.doi.org/10.1007/s00415-020-09825-0 |
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author | Gibson, Lucy L. McKeever, Anna Cullen, Alexis E. Nicholson, Timothy R. Aarsland, Dag Zandi, Michael S. Pollak, Thomas A. |
author_facet | Gibson, Lucy L. McKeever, Anna Cullen, Alexis E. Nicholson, Timothy R. Aarsland, Dag Zandi, Michael S. Pollak, Thomas A. |
author_sort | Gibson, Lucy L. |
collection | PubMed |
description | INTRODUCTION: Neuronal antibodies can cause encephalopathy syndromes often presenting with subacute cognitive impairment, sometimes resembling neurodegenerative dementias. METHODS: We searched Medline and Embase for studies reporting associations between neuronal surface antibodies in all-cause dementia versus controls. Random-effects meta-analysis was used to pool adjusted estimates across studies. RESULTS: Six studies were included, all reporting frequency of serum NMDAR antibodies in dementia with four also reporting frequency in atypical dementias. Both IgG [OR = 8.09 (1.51; 56.85), p = 0.036] and IgA/IgM NMDAR antibodies [OR = 42.48 (11.39; 158.52), p < 0.001] were associated with atypical dementia, but neither were associated with all-cause dementia. DISCUSSION: In the first meta-analysis to explore this literature, serum IgG and IgA/IgM NMDAR antibodies were significantly more common in atypical dementias. However, methodological issues and small-sample sizes necessitate caution interpreting this result. Further studies measuring both serum and CSF antibodies are needed to investigate the role of neuronal antibodies in dementia, since evidence of pathogenicity in even a subset of patients could pave the way for novel treatment options. |
format | Online Article Text |
id | pubmed-8289796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-82897962021-08-05 Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis Gibson, Lucy L. McKeever, Anna Cullen, Alexis E. Nicholson, Timothy R. Aarsland, Dag Zandi, Michael S. Pollak, Thomas A. J Neurol Review INTRODUCTION: Neuronal antibodies can cause encephalopathy syndromes often presenting with subacute cognitive impairment, sometimes resembling neurodegenerative dementias. METHODS: We searched Medline and Embase for studies reporting associations between neuronal surface antibodies in all-cause dementia versus controls. Random-effects meta-analysis was used to pool adjusted estimates across studies. RESULTS: Six studies were included, all reporting frequency of serum NMDAR antibodies in dementia with four also reporting frequency in atypical dementias. Both IgG [OR = 8.09 (1.51; 56.85), p = 0.036] and IgA/IgM NMDAR antibodies [OR = 42.48 (11.39; 158.52), p < 0.001] were associated with atypical dementia, but neither were associated with all-cause dementia. DISCUSSION: In the first meta-analysis to explore this literature, serum IgG and IgA/IgM NMDAR antibodies were significantly more common in atypical dementias. However, methodological issues and small-sample sizes necessitate caution interpreting this result. Further studies measuring both serum and CSF antibodies are needed to investigate the role of neuronal antibodies in dementia, since evidence of pathogenicity in even a subset of patients could pave the way for novel treatment options. Springer Berlin Heidelberg 2020-04-18 2021 /pmc/articles/PMC8289796/ /pubmed/32306172 http://dx.doi.org/10.1007/s00415-020-09825-0 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Gibson, Lucy L. McKeever, Anna Cullen, Alexis E. Nicholson, Timothy R. Aarsland, Dag Zandi, Michael S. Pollak, Thomas A. Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
title | Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
title_full | Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
title_fullStr | Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
title_full_unstemmed | Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
title_short | Neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
title_sort | neuronal surface autoantibodies in dementia: a systematic review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289796/ https://www.ncbi.nlm.nih.gov/pubmed/32306172 http://dx.doi.org/10.1007/s00415-020-09825-0 |
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