Evaluation of the Diagnostic and Predictive Value of Serum Levels of ANT1, ATG5, and Parkin in Multiple Sclerosis.


Journal

Clinical neurology and neurosurgery
ISSN: 1872-6968
Titre abrégé: Clin Neurol Neurosurg
Pays: Netherlands
ID NLM: 7502039

Informations de publication

Date de publication:
10 2020
Historique:
received: 30 06 2020
revised: 26 08 2020
accepted: 27 08 2020
pubmed: 6 9 2020
medline: 23 6 2021
entrez: 5 9 2020
Statut: ppublish

Résumé

Multiple Sclerosis (MS) is a disease of the central nervous system, which ultimately may lead to various disabilities in patients. No definitive cure has yet been developed for the disease. MRI is the method of choice for imaging MS plaques, which would be useful in disease diagnosis as it becomes progressive. Therefore, this study aimed to investigate the serum levels of ANT1 (adenine nucleotide translocase 1), ATG5 (autophagy-related protein 5), and Parkin in patients with MS, all of which play essential roles in MS pathophysiology, as novel serum biomarkers for early diagnosis of the disease. Forty patients in the early stages of the disease, and 40 healthy individuals were selected as the case and control groups. Upon sampling, the serum levels of the biomarkers were measured. The results indicated that autophagy, mitophagy, and mitochondrial apoptosis were different in the case and control groups. The oxidative stress level evaluation revealed low concertation of total antioxidant status (TAS) in the MS patients, while a partial increase accompanied the malondialdehyde (MDA). No significant correlation was observed between oxidative stress and autophagy or mitophagy factors. According to the results obtained from this study, the evaluation of serum levels of ANT1, ATG5, and Parkin could be applied in the diagnosis and follow-up of MS patients.

Identifiants

pubmed: 32890892
pii: S0303-8467(20)30540-0
doi: 10.1016/j.clineuro.2020.106197
pii:
doi:

Substances chimiques

ATG5 protein, human 0
Adenine Nucleotide Translocator 1 0
Autophagy-Related Protein 5 0
Biomarkers 0
SLC25A4 protein, human 0
Ubiquitin-Protein Ligases EC 2.3.2.27
parkin protein EC 2.3.2.27

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106197

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Omid Joodi Khanghah (O)

Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran; Department of Biochemistry and Clinical Laboratories, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Alireza Nourazarian (A)

Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran; Department of Biochemistry and Clinical Laboratories, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: alinour65@gmail.com.

Fatemeh Khaki-Khatibi (F)

Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran; Department of Biochemistry and Clinical Laboratories, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Masoud Nikanfar (M)

Department of Neurology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Delara Laghousi (D)

Social Determinants of Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Amir Mansour Vatankhah (AM)

Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Sepideh Moharami (S)

Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran; Department of Biochemistry and Clinical Laboratories, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

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Classifications MeSH