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CHAT gene polymorphism rs3810950 is associated with the risk of Alzheimer's disease in the Czech population
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SYSNO ASEP 0494766 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název CHAT gene polymorphism rs3810950 is associated with the risk of Alzheimer's disease in the Czech population Tvůrce(i) Hálová, A. (CZ)
Janoutová, J. (CZ)
Ewerlingová, Laura (UZFG-Y)
Janout, V. (CZ)
Bonczek, Ondřej (UZFG-Y)
Zeman, Tomáš (UZFG-Y) ORCID
Gerguri, T. (GB)
Balcar, Vladimír Josef (UZFG-Y) ORCID
Šerý, Omar (UZFG-Y) RIDČíslo článku 41 Zdroj.dok. Journal of Biomedical Science. - : BioMed Central - ISSN 1021-7770
Roč. 25, č. 1 (2018)Poč.str. 9 s. Forma vydání Tištěná - P Jazyk dok. eng - angličtina Země vyd. NL - Nizozemsko Klíč. slova Alzheimer´s disease ; polymorphism ; gene Vědní obor RIV FH - Neurologie, neurochirurgie, neurovědy Obor OECD Neurosciences (including psychophysiology Institucionální podpora UZFG-Y - RVO:67985904 UT WOS 000432822700001 EID SCOPUS 85047014440 DOI 10.1186/s12929-018-0444-2 Anotace Cholinergic hypothesis of Alzheimer's disease (AD) is based on the findings that a reduced and/or perturbed cholinergic activity in the central nervous system correlates with cognitive decline in patients with Alzheimer's disease. The hypothesis resulted in the development of centrally-acting agents potentiating cholinergic neurotransmission, these drugs, however, only slowed down the cognitive decline and could not prevent it Consequently, the perturbation of the central cholinergic signalling has been accepted as a part of the Alzheimer's aetiology but not necessarily the primary cause of the disease. In the present study we have focused on the rs3810950 polymorphism of ChAT (choline acetyltransferase) gene that has not been studied in Czech population befor.We carried out an association study to test for a relationship between the rs3810950 polymorphism arid Alzheimer's disease in a group of 1186 persons, 759 patients with Alzheimer's disease and 427 control subjects. Furthermore, we performed molecular modelling of the terminal domain (1st-126th amino acid residue) of one of the ChAT isoforms (M) to visualise in silico whether the rs3810950 polymorphism (A120T) can change any features of the tertiary structure of the protein which would have a potential to alter its function.
The AA genotype of CHAT was associated with a 1.25 times higher risk of AD (p < 0.002) thus demonstrating that the rs3810950 polymorphism can have a modest but statistically significant effect on the risk of AD in the Czech population. Furthermore, the molecular modelling indicated that the polymorphism is likely to be associated with significant variations in the tertiary structure of the protein molecule which may impact its enzyme activity. Our findings are consistent with the results of the meta-analytical studies of the relationship between rs3810950 polymorphism and AD and provide further material evidence for a direct (primary) involvement of cholinergic mechanisms in the etiopathogenesis of AD, particularly as a factor in cognitive decline and perturbed conscious awareness commonly observed in patients with AD.Pracoviště Ústav živočišné fyziologie a genetiky Kontakt Jana Zásmětová, knihovna@iapg.cas.cz, Tel.: 315 639 554 Rok sběru 2019
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