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Clinical biomarkers for Lewy body diseases
Synucleinopathies are a group of neurodegenerative disorders characterized by pathologic aggregates of neural and glial α-synuclein (α-syn) in the form of Lewy bodies (LBs), Lewy neurites, and cytoplasmic inclusions in both neurons and glia. Two major classes of synucleinopathies are LB disease and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644566/ https://www.ncbi.nlm.nih.gov/pubmed/37964309 http://dx.doi.org/10.1186/s13578-023-01152-x |
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author | Abdelmoaty, Mai M. Lu, Eugene Kadry, Rana Foster, Emma G. Bhattarai, Shaurav Mosley, R. Lee Gendelman, Howard E. |
author_facet | Abdelmoaty, Mai M. Lu, Eugene Kadry, Rana Foster, Emma G. Bhattarai, Shaurav Mosley, R. Lee Gendelman, Howard E. |
author_sort | Abdelmoaty, Mai M. |
collection | PubMed |
description | Synucleinopathies are a group of neurodegenerative disorders characterized by pathologic aggregates of neural and glial α-synuclein (α-syn) in the form of Lewy bodies (LBs), Lewy neurites, and cytoplasmic inclusions in both neurons and glia. Two major classes of synucleinopathies are LB disease and multiple system atrophy. LB diseases include Parkinson’s disease (PD), PD with dementia, and dementia with LBs. All are increasing in prevalence. Effective diagnostics, disease-modifying therapies, and therapeutic monitoring are urgently needed. Diagnostics capable of differentiating LB diseases are based on signs and symptoms which might overlap. To date, no specific diagnostic test exists despite disease-specific pathologies. Diagnostics are aided by brain imaging and cerebrospinal fluid evaluations, but more accessible biomarkers remain in need. Mechanisms of α-syn evolution to pathologic oligomers and insoluble fibrils can provide one of a spectrum of biomarkers to link complex neural pathways to effective therapies. With these in mind, we review promising biomarkers linked to effective disease-modifying interventions. |
format | Online Article Text |
id | pubmed-10644566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106445662023-11-14 Clinical biomarkers for Lewy body diseases Abdelmoaty, Mai M. Lu, Eugene Kadry, Rana Foster, Emma G. Bhattarai, Shaurav Mosley, R. Lee Gendelman, Howard E. Cell Biosci Review Synucleinopathies are a group of neurodegenerative disorders characterized by pathologic aggregates of neural and glial α-synuclein (α-syn) in the form of Lewy bodies (LBs), Lewy neurites, and cytoplasmic inclusions in both neurons and glia. Two major classes of synucleinopathies are LB disease and multiple system atrophy. LB diseases include Parkinson’s disease (PD), PD with dementia, and dementia with LBs. All are increasing in prevalence. Effective diagnostics, disease-modifying therapies, and therapeutic monitoring are urgently needed. Diagnostics capable of differentiating LB diseases are based on signs and symptoms which might overlap. To date, no specific diagnostic test exists despite disease-specific pathologies. Diagnostics are aided by brain imaging and cerebrospinal fluid evaluations, but more accessible biomarkers remain in need. Mechanisms of α-syn evolution to pathologic oligomers and insoluble fibrils can provide one of a spectrum of biomarkers to link complex neural pathways to effective therapies. With these in mind, we review promising biomarkers linked to effective disease-modifying interventions. BioMed Central 2023-11-14 /pmc/articles/PMC10644566/ /pubmed/37964309 http://dx.doi.org/10.1186/s13578-023-01152-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Abdelmoaty, Mai M. Lu, Eugene Kadry, Rana Foster, Emma G. Bhattarai, Shaurav Mosley, R. Lee Gendelman, Howard E. Clinical biomarkers for Lewy body diseases |
title | Clinical biomarkers for Lewy body diseases |
title_full | Clinical biomarkers for Lewy body diseases |
title_fullStr | Clinical biomarkers for Lewy body diseases |
title_full_unstemmed | Clinical biomarkers for Lewy body diseases |
title_short | Clinical biomarkers for Lewy body diseases |
title_sort | clinical biomarkers for lewy body diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644566/ https://www.ncbi.nlm.nih.gov/pubmed/37964309 http://dx.doi.org/10.1186/s13578-023-01152-x |
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