Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure

Aim. To study the impact of a polymorphic variant of the matrix metalloproteinase-3 (MMP-3) gene on the development and course of chronic heart failure (CHF) in patients with coronary heart disease. Subjects and methods. A total of 277 patients with New York Heart Association (NYHA) Functional Class...

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Main Authors: A T Teplyakov, E N Berezikova, S N Shilov, E V Grakova, Yu Yu Torim, A V Efremov, I D Safronov, M G Pustovetova, R S Karpov
Format: Article
Language:Russian
Published: "Consilium Medicum" Publishing house 2015-04-01
Series:Терапевтический архив
Subjects:
Online Access:https://ter-arkhiv.ru/0040-3660/article/view/31704
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author A T Teplyakov
E N Berezikova
S N Shilov
E V Grakova
Yu Yu Torim
A V Efremov
I D Safronov
M G Pustovetova
R S Karpov
author_facet A T Teplyakov
E N Berezikova
S N Shilov
E V Grakova
Yu Yu Torim
A V Efremov
I D Safronov
M G Pustovetova
R S Karpov
author_sort A T Teplyakov
collection DOAJ
description Aim. To study the impact of a polymorphic variant of the matrix metalloproteinase-3 (MMP-3) gene on the development and course of chronic heart failure (CHF) in patients with coronary heart disease. Subjects and methods. A total of 277 patients with New York Heart Association (NYHA) Functional Class (FC) II—IV CHF were examined. MMP-3 –1171 5A/6A genetic polymorphism was studied by polymerase chain reaction. A control group included 136 patients (mean age 53.6±4.8 years) with no signs of cardiovascular diseases, as evidenced by the examination. Results. The frequency of the 5A allele and the 5A/5A genotype of the 1171 5A/6A polymorphic locus in the MMP-3 gene proved to be higher in the patients with CHF than that in the control group. Thus, the variability of the 5A allele (odds ratio (OR), 1.39; 95% confidence interval (CI): 1.033 to 1.869; p=0.03) and the 5A/5A genotype (OR, 2.15; 95% CI: 1.131 to 4.070; p=0.02) was associated with increased risk for CHF. There were significant differences in the frequency of MMP-3 alleles and genotypes in relation to FC of CHF. The frequency of the 5A/5A genotype was substantially higher in the patients with NYHA FC IV CHF than that in those with NYHA FC II CHF (32.8% versus 15.2%; р=0.039). The frequency of the 5A allele was significantly higher in the patients with NYHA FC IV CHF than that in those with NYHA FC II CHF (55.5% and 39.3%; respectively; р=0.019). Thus, the carriage of the 5A allele and the 5A/5A genotype of the 1171 5A/6A polymorphic locus in the MMP-3 gene is a risk factor of severe CHF. Conclusion. The determination of ММР-3 –1171 5A/6A polymorphism may be recommended for the early prediction of a risk for the development and severe course of CHF.
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spelling doaj.art-a39a8638f4be4f669f7b68139117e01f2022-12-21T18:46:59Zrus"Consilium Medicum" Publishing houseТерапевтический архив0040-36602309-53422015-04-0187481228720Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failureA T TeplyakovE N BerezikovaS N ShilovE V GrakovaYu Yu TorimA V EfremovI D SafronovM G PustovetovaR S KarpovAim. To study the impact of a polymorphic variant of the matrix metalloproteinase-3 (MMP-3) gene on the development and course of chronic heart failure (CHF) in patients with coronary heart disease. Subjects and methods. A total of 277 patients with New York Heart Association (NYHA) Functional Class (FC) II—IV CHF were examined. MMP-3 –1171 5A/6A genetic polymorphism was studied by polymerase chain reaction. A control group included 136 patients (mean age 53.6±4.8 years) with no signs of cardiovascular diseases, as evidenced by the examination. Results. The frequency of the 5A allele and the 5A/5A genotype of the 1171 5A/6A polymorphic locus in the MMP-3 gene proved to be higher in the patients with CHF than that in the control group. Thus, the variability of the 5A allele (odds ratio (OR), 1.39; 95% confidence interval (CI): 1.033 to 1.869; p=0.03) and the 5A/5A genotype (OR, 2.15; 95% CI: 1.131 to 4.070; p=0.02) was associated with increased risk for CHF. There were significant differences in the frequency of MMP-3 alleles and genotypes in relation to FC of CHF. The frequency of the 5A/5A genotype was substantially higher in the patients with NYHA FC IV CHF than that in those with NYHA FC II CHF (32.8% versus 15.2%; р=0.039). The frequency of the 5A allele was significantly higher in the patients with NYHA FC IV CHF than that in those with NYHA FC II CHF (55.5% and 39.3%; respectively; р=0.019). Thus, the carriage of the 5A allele and the 5A/5A genotype of the 1171 5A/6A polymorphic locus in the MMP-3 gene is a risk factor of severe CHF. Conclusion. The determination of ММР-3 –1171 5A/6A polymorphism may be recommended for the early prediction of a risk for the development and severe course of CHF.https://ter-arkhiv.ru/0040-3660/article/view/31704heart failurecoronary heart diseasegenetic polymorphismmatrix metalloproteinase-3
spellingShingle A T Teplyakov
E N Berezikova
S N Shilov
E V Grakova
Yu Yu Torim
A V Efremov
I D Safronov
M G Pustovetova
R S Karpov
Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
Терапевтический архив
heart failure
coronary heart disease
genetic polymorphism
matrix metalloproteinase-3
title Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
title_full Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
title_fullStr Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
title_full_unstemmed Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
title_short Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
title_sort assessment of the role of matrix metalloproteinase 2 gene polymorphism in the development of chronic heart failure
topic heart failure
coronary heart disease
genetic polymorphism
matrix metalloproteinase-3
url https://ter-arkhiv.ru/0040-3660/article/view/31704
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