Clinical biomarkers for Lewy body diseases

Abstract 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 dis...

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Main Authors: Mai M. Abdelmoaty, Eugene Lu, Rana Kadry, Emma G. Foster, Shaurav Bhattarai, R. Lee Mosley, Howard E. Gendelman
Format: Article
Language:English
Published: BMC 2023-11-01
Series:Cell & Bioscience
Subjects:
Online Access:https://doi.org/10.1186/s13578-023-01152-x
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author Mai M. Abdelmoaty
Eugene Lu
Rana Kadry
Emma G. Foster
Shaurav Bhattarai
R. Lee Mosley
Howard E. Gendelman
author_facet Mai M. Abdelmoaty
Eugene Lu
Rana Kadry
Emma G. Foster
Shaurav Bhattarai
R. Lee Mosley
Howard E. Gendelman
author_sort Mai M. Abdelmoaty
collection DOAJ
description Abstract 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.
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spelling doaj.art-2c505cc77c0f419ab35ba80333b7b3fd2023-11-20T11:03:58ZengBMCCell & Bioscience2045-37012023-11-0113112310.1186/s13578-023-01152-xClinical biomarkers for Lewy body diseasesMai M. Abdelmoaty0Eugene Lu1Rana Kadry2Emma G. Foster3Shaurav Bhattarai4R. Lee Mosley5Howard E. Gendelman6Department of Pharmacology and Experimental Neuroscience, College of Medicine, University of Nebraska Medical CenterDepartment of Pharmacology and Experimental Neuroscience, College of Medicine, University of Nebraska Medical CenterDepartment of Cellular and Integrative Physiology, University of Nebraska Medical CenterDepartment of Pharmacology and Experimental Neuroscience, College of Medicine, University of Nebraska Medical CenterDepartment of Pharmacology and Experimental Neuroscience, College of Medicine, University of Nebraska Medical CenterDepartment of Pharmacology and Experimental Neuroscience, College of Medicine, University of Nebraska Medical CenterDepartment of Pharmacology and Experimental Neuroscience, College of Medicine, University of Nebraska Medical CenterAbstract 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.https://doi.org/10.1186/s13578-023-01152-xSynucleinopathiesParkinson’s diseaseParkinson’s disease with dementiaDementia with Lewy bodiesα-synucleinBiomarkers
spellingShingle Mai M. Abdelmoaty
Eugene Lu
Rana Kadry
Emma G. Foster
Shaurav Bhattarai
R. Lee Mosley
Howard E. Gendelman
Clinical biomarkers for Lewy body diseases
Cell & Bioscience
Synucleinopathies
Parkinson’s disease
Parkinson’s disease with dementia
Dementia with Lewy bodies
α-synuclein
Biomarkers
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 Synucleinopathies
Parkinson’s disease
Parkinson’s disease with dementia
Dementia with Lewy bodies
α-synuclein
Biomarkers
url https://doi.org/10.1186/s13578-023-01152-x
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