Analysis of the effect of N5, N10-methylenetetrahydrofolate reductase gene C(677)-->T polymorphism on the ischemic stroke development in persons with various risk factors
Harbuzova VIu1, Polonikov OV1, Stroĭ DO3, Matlaĭ OI1, Ataman IuO1, Sukharieva VA2, Ataman OV1
- Sumy University, Sumy, Ukraine;
- Kursk Medical University, Russia;
- O.O. Bogomoletz Institute of Physiology, Kyiv, Ukriane
DOI: https://doi.org/10.15407/fz60.02.018
Abstract
The results of MTHFR gene C677T (rs1801133) polymorphism
determined in 170 patients with ischemic atherothrombotic
stroke (IATS) and 124 healthy subjects (control group) are
presented in the paper. It has been shown that in patients with
IATS, the frequencies of main homozygotes (CC), heterozygotes
(CT) and minor homozygotes (TT) are 52.4, 35.9,
11.8% (in control – 46.0, 48.4, 5.6%, P=0.044 by ?2-test). TT
homozygotes have a greater chance of developing IATS than
carriers of main C-allele (CT + CC) (OR = 2.3, CI = 0.911-
5.449, P = 0.049). In the representatives of the Ukrainian
population there is a relationship between the frequency of
MTHFR gene C677T polymorphism genotypes and the risk
of IATS. This connection is manifested in male patients, in
persons with normal blood pressure, and in people who do
not have the habit of smoking. The sex of the patients, body
mass index, blood pressure and smoking affect the level of the
studied polymorphism association with stroke.
Keywords:
methylenetetrahydrofolate reductase, genes polymorphism,ischemic stroke.
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