Pursuing Multiple Biomarkers for Early Idiopathic Parkinson's Disease Diagnosis.


Journal

Molecular neurobiology
ISSN: 1559-1182
Titre abrégé: Mol Neurobiol
Pays: United States
ID NLM: 8900963

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 09 04 2021
accepted: 16 07 2021
pubmed: 6 8 2021
medline: 25 3 2022
entrez: 5 8 2021
Statut: ppublish

Résumé

Parkinson's disease (PD) ranks first in the world as a neurodegenerative movement disorder and occurs most commonly in an idiopathic form. PD patients may have motor symptoms, non-motor symptoms, including cognitive and behavioral changes, and symptoms related to autonomic nervous system (ANS) failures, such as gastrointestinal, urinary, and cardiovascular symptoms. Unfortunately, the diagnostic accuracy of PD by general neurologists is relatively low. Currently, there is no objective molecular or biochemical test for PD; its diagnosis is based on clinical criteria, mainly by cardinal motor symptoms, which manifest when patients have lost about 60-80% of dopaminergic neurons. Therefore, it is urgent to establish a panel of biomarkers for the early and accurate diagnosis of PD. Once the disease is accurately diagnosed, it may be easier to unravel idiopathic PD's pathogenesis, and ultimately, finding a cure. This review discusses several biomarkers' potential to set a panel for early idiopathic PD diagnosis and future directions.

Identifiants

pubmed: 34350555
doi: 10.1007/s12035-021-02500-z
pii: 10.1007/s12035-021-02500-z
doi:

Substances chimiques

Biomarkers 0
alpha-Synuclein 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

5517-5532

Subventions

Organisme : programa de apoyo a la investigación científica y tecnológica
ID : SA1872-21
Organisme : programa de apoyo a la investigación científica y tecnológica
ID : SA1891-21

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Yareth Gopar-Cuevas (Y)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico.

Ana P Duarte-Jurado (AP)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico.

Rosa N Diaz-Perez (RN)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico.

Odila Saucedo-Cardenas (O)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico.
Departamento de Genética Molecular, Centro de Investigación Biomédica del Noreste, Delegación Nuevo León, Instituto Mexicano del Seguro Social, Monterrey, Mexico.

Maria J Loera-Arias (MJ)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico.

Roberto Montes-de-Oca-Luna (R)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico.

Humberto Rodriguez-Rocha (H)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico. humberto.rodriguezrc@uanl.edu.mx.

Aracely Garcia-Garcia (A)

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, 64460, Monterrey, Mexico. aracely.garciagr@uanl.edu.mx.

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