Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis

Aim. To study a contribution of polymorphism A-8202G (rs11697325) of a gene of matrix metalloproteinase-9 (MMP-9) in development of arterial hypertension (AH) in patients with the rheumatoid arthritis (RA). Materail and methods. 143 patients with RA were examined, among which a group of patients...

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Main Authors: Svetlana Yu. Nikulina, Anna A. Chernova, Yuliya A. Tolstokorova, Yulia O. Varavko
Format: Article
Language:English
Published: Concilium Medicum 2022-12-01
Series:КардиоСоматика
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Online Access:https://cardiosomatics.orscience.ru/2221-7185/article/viewFile/110917/pdf
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author Svetlana Yu. Nikulina
Anna A. Chernova
Yuliya A. Tolstokorova
Yulia O. Varavko
author_facet Svetlana Yu. Nikulina
Anna A. Chernova
Yuliya A. Tolstokorova
Yulia O. Varavko
author_sort Svetlana Yu. Nikulina
collection DOAJ
description Aim. To study a contribution of polymorphism A-8202G (rs11697325) of a gene of matrix metalloproteinase-9 (MMP-9) in development of arterial hypertension (AH) in patients with the rheumatoid arthritis (RA). Materail and methods. 143 patients with RA were examined, among which a group of patients with RA without AH (n=50) and a group of patients with RA in association with AH (n=93) were identified. Healthy volunteers (n=151) were also divided into 2 groups comparable in age, sex and number with the main groups (control group 1 n=54, control group 2 n=97). The work used a range of clinical, laboratory, instrumental methods. A molecular genetic study was also performed. Blood samples were taken from all study participants. DNA isolation was carried out by the standard phenol-chloroform method. Genotyping for the MMP-9 gene was performed by PCR-RFLP analysis (polymerase chain reaction restriction fragment length polymorphism). PCR was carried out with a set of primers to the corresponding regions of the genome. PCR products were analyzed by electrophoresis in 4% polyacrylamide gel followed by staining with ethidium bromide. Results. In the course of a molecular genetic study, a statistically significant predominance of the homozygous AA genotype and the A allele of the MMP-9 (rs11697325) gene polymorphism was observed in the group of patients with RA, both separately and in association with AH, in comparison with the data of control groups. The risk of developing RA estimated by the odds ratio (OR) in carriers of the AA genotype of the MMP-9 gene is 1.8 times higher (95% confidence interval CI 1.1362.950; p=0.02) than in carriers of the GG and GA genotypes; in carriers of the A allele, the risk of developing RA is 1.6 times higher compared to the G allele (95% CI 1.1192.578; p=0.01). The OR risk of developing RA in association with hypertension in carriers of the AA genotype of the MMP-9 gene is 2.8 times higher (95% CI 1.2836.54; p=0.04) compared to GA and GG genotypes, 2.1 times higher in carriers of the A allele (95% CI 1.1134.127; p=0.02) compared to the G allele. Conclusion. Thus, the results of the study indicate that the homozygous AA genotype and the A allele of the MMP-9 (rs11697325) gene polymorphism are the predictors of the development of RA both as a separate nosological unit and in association with AH.
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spelling doaj.art-19f0efe61fc748f781f09e44f2e2907c2022-12-22T04:41:20ZengConcilium MedicumКардиоСоматика2221-71852658-57072022-12-01132768010.17816/CS11091776508Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritisSvetlana Yu. Nikulina0https://orcid.org/0000-0002-6968-7627Anna A. Chernova1https://orcid.org/0000-0003-2977-1792Yuliya A. Tolstokorova2https://orcid.org/0000-0002-2261-0868Yulia O. Varavko3https://orcid.org/0000-0002-8524-7584Voino-Yasenetsky Krasnoyarsk State Medical UniversityVoino-Yasenetsky Krasnoyarsk State Medical UniversityVoino-Yasenetsky Krasnoyarsk State Medical UniversityIrkutsk State Medical UniversityAim. To study a contribution of polymorphism A-8202G (rs11697325) of a gene of matrix metalloproteinase-9 (MMP-9) in development of arterial hypertension (AH) in patients with the rheumatoid arthritis (RA). Materail and methods. 143 patients with RA were examined, among which a group of patients with RA without AH (n=50) and a group of patients with RA in association with AH (n=93) were identified. Healthy volunteers (n=151) were also divided into 2 groups comparable in age, sex and number with the main groups (control group 1 n=54, control group 2 n=97). The work used a range of clinical, laboratory, instrumental methods. A molecular genetic study was also performed. Blood samples were taken from all study participants. DNA isolation was carried out by the standard phenol-chloroform method. Genotyping for the MMP-9 gene was performed by PCR-RFLP analysis (polymerase chain reaction restriction fragment length polymorphism). PCR was carried out with a set of primers to the corresponding regions of the genome. PCR products were analyzed by electrophoresis in 4% polyacrylamide gel followed by staining with ethidium bromide. Results. In the course of a molecular genetic study, a statistically significant predominance of the homozygous AA genotype and the A allele of the MMP-9 (rs11697325) gene polymorphism was observed in the group of patients with RA, both separately and in association with AH, in comparison with the data of control groups. The risk of developing RA estimated by the odds ratio (OR) in carriers of the AA genotype of the MMP-9 gene is 1.8 times higher (95% confidence interval CI 1.1362.950; p=0.02) than in carriers of the GG and GA genotypes; in carriers of the A allele, the risk of developing RA is 1.6 times higher compared to the G allele (95% CI 1.1192.578; p=0.01). The OR risk of developing RA in association with hypertension in carriers of the AA genotype of the MMP-9 gene is 2.8 times higher (95% CI 1.2836.54; p=0.04) compared to GA and GG genotypes, 2.1 times higher in carriers of the A allele (95% CI 1.1134.127; p=0.02) compared to the G allele. Conclusion. Thus, the results of the study indicate that the homozygous AA genotype and the A allele of the MMP-9 (rs11697325) gene polymorphism are the predictors of the development of RA both as a separate nosological unit and in association with AH.https://cardiosomatics.orscience.ru/2221-7185/article/viewFile/110917/pdfrheumatoid arthritiscardiovascular pathologyarterial hypertensionmolecular and genetic researchone-nucleotide polymorphismassociation of genes
spellingShingle Svetlana Yu. Nikulina
Anna A. Chernova
Yuliya A. Tolstokorova
Yulia O. Varavko
Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis
КардиоСоматика
rheumatoid arthritis
cardiovascular pathology
arterial hypertension
molecular and genetic research
one-nucleotide polymorphism
association of genes
title Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis
title_full Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis
title_fullStr Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis
title_full_unstemmed Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis
title_short Associative role of polymorphism of the gene of <i>MMP-9</i> (rs11697325) in development of arterial hypertension in patients with the rheumatoid arthritis
title_sort associative role of polymorphism of the gene of i mmp 9 i rs11697325 in development of arterial hypertension in patients with the rheumatoid arthritis
topic rheumatoid arthritis
cardiovascular pathology
arterial hypertension
molecular and genetic research
one-nucleotide polymorphism
association of genes
url https://cardiosomatics.orscience.ru/2221-7185/article/viewFile/110917/pdf
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