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Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography

BACKGROUND: Pathogenic autoantibodies targeting the recently identified leucine rich glioma inactivated 1 protein and the subunit 1 of the N-methyl-D-aspartate receptor induce autoimmune encephalitis. A comparison of brain metabolic patterns in (18)F-fluoro-2-deoxy-d-glucose positron emission tomogr...

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Autores principales: Wegner, Florian, Wilke, Florian, Raab, Peter, Tayeb, Said Ben, Boeck, Anna-Lena, Haense, Cathleen, Trebst, Corinna, Voss, Elke, Schrader, Christoph, Logemann, Frank, Ahrens, Jörg, Leffler, Andreas, Rodriguez-Raecke, Rea, Dengler, Reinhard, Geworski, Lilli, Bengel, Frank M, Berding, Georg, Stangel, Martin, Nabavi, Elham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076767/
https://www.ncbi.nlm.nih.gov/pubmed/24950993
http://dx.doi.org/10.1186/1471-2377-14-136
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author Wegner, Florian
Wilke, Florian
Raab, Peter
Tayeb, Said Ben
Boeck, Anna-Lena
Haense, Cathleen
Trebst, Corinna
Voss, Elke
Schrader, Christoph
Logemann, Frank
Ahrens, Jörg
Leffler, Andreas
Rodriguez-Raecke, Rea
Dengler, Reinhard
Geworski, Lilli
Bengel, Frank M
Berding, Georg
Stangel, Martin
Nabavi, Elham
author_facet Wegner, Florian
Wilke, Florian
Raab, Peter
Tayeb, Said Ben
Boeck, Anna-Lena
Haense, Cathleen
Trebst, Corinna
Voss, Elke
Schrader, Christoph
Logemann, Frank
Ahrens, Jörg
Leffler, Andreas
Rodriguez-Raecke, Rea
Dengler, Reinhard
Geworski, Lilli
Bengel, Frank M
Berding, Georg
Stangel, Martin
Nabavi, Elham
author_sort Wegner, Florian
collection PubMed
description BACKGROUND: Pathogenic autoantibodies targeting the recently identified leucine rich glioma inactivated 1 protein and the subunit 1 of the N-methyl-D-aspartate receptor induce autoimmune encephalitis. A comparison of brain metabolic patterns in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography of anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis patients has not been performed yet and shall be helpful in differentiating these two most common forms of autoimmune encephalitis. METHODS: The brain (18)F-fluoro-2-deoxy-d-glucose uptake from whole-body positron emission tomography of six anti-N-methyl-D-aspartate receptor encephalitis patients and four patients with anti-leucine rich glioma inactivated 1 protein encephalitis admitted to Hannover Medical School between 2008 and 2012 was retrospectively analyzed and compared to matched controls. RESULTS: Group analysis of anti-N-methyl-D-aspartate encephalitis patients demonstrated regionally limited hypermetabolism in frontotemporal areas contrasting an extensive hypometabolism in parietal lobes, whereas the anti-leucine rich glioma inactivated 1 protein syndrome was characterized by hypermetabolism in cerebellar, basal ganglia, occipital and precentral areas and minor frontomesial hypometabolism. CONCLUSIONS: This retrospective (18)F-fluoro-2-deoxy-d-glucose positron emission tomography study provides novel evidence for distinct brain metabolic patterns in patients with anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis.
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spelling pubmed-40767672014-07-02 Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography Wegner, Florian Wilke, Florian Raab, Peter Tayeb, Said Ben Boeck, Anna-Lena Haense, Cathleen Trebst, Corinna Voss, Elke Schrader, Christoph Logemann, Frank Ahrens, Jörg Leffler, Andreas Rodriguez-Raecke, Rea Dengler, Reinhard Geworski, Lilli Bengel, Frank M Berding, Georg Stangel, Martin Nabavi, Elham BMC Neurol Research Article BACKGROUND: Pathogenic autoantibodies targeting the recently identified leucine rich glioma inactivated 1 protein and the subunit 1 of the N-methyl-D-aspartate receptor induce autoimmune encephalitis. A comparison of brain metabolic patterns in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography of anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis patients has not been performed yet and shall be helpful in differentiating these two most common forms of autoimmune encephalitis. METHODS: The brain (18)F-fluoro-2-deoxy-d-glucose uptake from whole-body positron emission tomography of six anti-N-methyl-D-aspartate receptor encephalitis patients and four patients with anti-leucine rich glioma inactivated 1 protein encephalitis admitted to Hannover Medical School between 2008 and 2012 was retrospectively analyzed and compared to matched controls. RESULTS: Group analysis of anti-N-methyl-D-aspartate encephalitis patients demonstrated regionally limited hypermetabolism in frontotemporal areas contrasting an extensive hypometabolism in parietal lobes, whereas the anti-leucine rich glioma inactivated 1 protein syndrome was characterized by hypermetabolism in cerebellar, basal ganglia, occipital and precentral areas and minor frontomesial hypometabolism. CONCLUSIONS: This retrospective (18)F-fluoro-2-deoxy-d-glucose positron emission tomography study provides novel evidence for distinct brain metabolic patterns in patients with anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis. BioMed Central 2014-06-20 /pmc/articles/PMC4076767/ /pubmed/24950993 http://dx.doi.org/10.1186/1471-2377-14-136 Text en Copyright © 2014 Wegner et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wegner, Florian
Wilke, Florian
Raab, Peter
Tayeb, Said Ben
Boeck, Anna-Lena
Haense, Cathleen
Trebst, Corinna
Voss, Elke
Schrader, Christoph
Logemann, Frank
Ahrens, Jörg
Leffler, Andreas
Rodriguez-Raecke, Rea
Dengler, Reinhard
Geworski, Lilli
Bengel, Frank M
Berding, Georg
Stangel, Martin
Nabavi, Elham
Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography
title Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography
title_full Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography
title_fullStr Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography
title_full_unstemmed Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography
title_short Anti-leucine rich glioma inactivated 1 protein and anti-N-methyl-D-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)F-fluoro-2-deoxy-d-glucose positron emission tomography
title_sort anti-leucine rich glioma inactivated 1 protein and anti-n-methyl-d-aspartate receptor encephalitis show distinct patterns of brain glucose metabolism in (18)f-fluoro-2-deoxy-d-glucose positron emission tomography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076767/
https://www.ncbi.nlm.nih.gov/pubmed/24950993
http://dx.doi.org/10.1186/1471-2377-14-136
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