Association of Polymorphic Genome Variants in the 2q32.1 Locus with the Development of Vasovagal Syncope

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Resumo

Vasovagal syncope (VVS) is the most common form of syncope. The mechanisms of VVS development are not entirely clear. It is known that there is a genetic predisposition to this disease, but the data on the role of individual genes are quite contradictory. Recently, a genome-wide association study identified a locus at chromosome 2q32.1 associated with a united group of diseases – syncope and collapse; among the single nucleotide polymorphisms (SNPs) of this locus, the most significant association was observed for rs12465214. In a homogeneous sample of patients according to the diagnosis of VVS, we analyzed the association of rs12465214, rs12621296, rs17582219 and rs1344706 located on chromosome 2q32.1, with this form of syncope. In the enrolled set, only rs12621296 was associated with VVS by itself, whereas associations of other SNPs were observed only in biallelic combinations. An epistatic interaction between the components of the combination rs12621296*A + rs17582219*A was revealed. The possible involvement of individual genes localized in the 2q32.1 locus in the genetic architecture of the VVS is discussed.

Sobre autores

N. Matveeva

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation; Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation

Autor responsável pela correspondência
Email: natalijamat@rambler.ru
Russia, 121552, Moscow; Russia, 117997, Moscow

B. Titov

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation; Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation

Email: natalijamat@rambler.ru
Russia, 121552, Moscow; Russia, 117997, Moscow

E. Bazyleva

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation

Email: natalijamat@rambler.ru
Russia, 121552, Moscow

Е. Kuchinskaya

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation

Email: natalijamat@rambler.ru
Russia, 121552, Moscow

M. Kozin

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation; Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation

Email: natalijamat@rambler.ru
Russia, 121552, Moscow; Russia, 117997, Moscow

A. Favorov

Johns Hopkins School of Medicine

Email: natalijamat@rambler.ru
USA, 21205, Baltimore, MD

A. Pevzner

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation

Email: natalijamat@rambler.ru
Russia, 121552, Moscow

O. Favorova

National Medical Research Center for Cardiology named after academician E.I. Chazov,
Ministry of Health of the Russian Federation; Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation

Email: natalijamat@rambler.ru
Russia, 121552, Moscow; Russia, 117997, Moscow

Bibliografia

  1. Matveeva N., Titov B., Bazyleva E., Pevzner A., Favorova O. (2021) Towards understanding the genetic nature of vasovagal syncope. Int. J. Mol. Sci. 22, 10316.
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Declaração de direitos autorais © Н.А. Матвеева, Б.В. Титов, Е.А. Базылева, Е.А. Кучинская, М.С. Козин, А.В. Фаворов, А.В. Певзнер, О.О. Фаворова, 2023

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