Analysis of ADORA2A, MTA1, PTGDS, PTGS2, NSF, and HNMT Gene Expression Levels in Peripheral Blood of Patients with Early Stages of Parkinson’s Disease

Author:

Semenova Ekaterina I.1ORCID,Partevian Suzanna A.1,Shulskaya Marina V.1,Rudenok Margarita M.1,Lukashevich Maria V.1,Baranova Nina M.2,Doronina Olga B.3,Doronina Kseniya S.3,Rosinskaya Anna V.4,Fedotova Ekaterina Y.5,Illarioshkin Sergey N.5,Slominsky Petr A.1,Shadrina Maria I.1,Alieva Anelya Kh.1

Affiliation:

1. National Research Centre “Kurchatov Institute”, 2 Kurchatova Sq., 123182 Moscow, Russia

2. Peoples’ Friendship University of Russia (RUDN University), 6, Miklukho-Maklaya Str., 117198 Moscow, Russia

3. Novosibirsk State Medical University, 52, Krasnyy Ave., 630091 Novosibirsk, Russia

4. State Public Health Institution Primorsk Regional Clinical Hospital No. 1, 57 Aleutskaya St., 690091 Vladivostok, Russia

5. Research Centre of Neurology, 80, Volokolamskoye Shosse, 125367 Moscow, Russia

Abstract

Parkinson’s disease (PD) is a common chronic, age-related neurodegenerative disease. This disease is characterized by a long prodromal period. In this context, it is important to search for the genes and mechanisms that are involved in the development of the pathological process in the earliest stages of the disease. Published data suggest that blood cells, particularly lymphocytes, may be a model for studying the processes that occur in the brain in PD. Thus, in the present work, we performed an analysis of changes in the expression of the genes ADORA2A, MTA1, PTGDS, PTGS2, NSF, and HNMT in the peripheral blood of patients with early stages of PD (stages 1 and 2 of the Hoehn–Yahr scale). We found significant and PD-specific expression changes of four genes, i.e., MTA1, PTGS2, NSF, and HNMT, in the peripheral blood of patients with early stages of PD. These genes may be associated with PD pathogenesis in the early clinical stages and can be considered as potential candidate genes for this disease. Altered expression of the ADORA2A gene in treated PD patients may indicate that this gene is involved in processes affected by antiparkinsonian therapy.

Funder

Federal Target Program

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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