Endothelium function biomarkers and carotid intima-media thickness changes in relation to NOS3 (rs2070744) and GNB3 (rs5443) genes polymorphism in the essential arterial hypertension

The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to (rs5443) and (rs2070744) genes polymorphism in the essential arterial hypertension (EAH). Methods. One-hundred EAH patients (48 – control) participated in...

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Published inEndocrine regulations (Bratislava) Vol. 56; no. 2; pp. 104 - 114
Main Authors Sydorchuk, Andrii R., Sydorchuk, Larysa P., Gutnitska, Adelina F., Dzhuryak, Valentina S., Kryvetska, Inna I., Sydorchuk, Ruslan I., Ursuliak, Yulia V., Iftoda, Oksana M.
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Abstract The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to (rs5443) and (rs2070744) genes polymorphism in the essential arterial hypertension (EAH). Methods. One-hundred EAH patients (48 – control) participated in the case-control study. Soluble vascular cell adhesion molecule (sVCAM-1), total NO metabolites (NO +NO ), transcriptional activity of gene, endothelium-dependent flow-mediated dilation of the brachial artery (FMD BA), and carotid IMT were studied. (rs5443) and (rs2070744) genotyping was performed by TaqMan probes (CFX96™Real-Time PCR). Results. The connection of (rs2070744) with decreased total NO metabolites (F=71.11; p<0.001), reduced genes transcription activity (F=8.71; p<0.001) and increased sVCAM-1 (F=6.96; p=0.002), especially in the -allele carriers (particularly in -genotype patients with lower NO – 16.46% and 40.88%; p<0.001), lowered the transcription activity of NOS3 gene – 46.03% 7 times (p<0.001), and become higher sVCAM-1 – 35.48% and 89.48% (p<0.001), respectively. ANOVA did not confirm the association of (rs5443) gene with endothelial function and carotid IMT. Severe EAH was associated with increased carotid IMT – 50.0% (p<0.001) and 57.14% (p=0.007), wider carotid arteries – 17.36% (p=0.012) and 21.79% (p=0.004), and decreased NOS3 genes transcription activity – 34.54% (p=0.003). Atherosclerotic plaques were unilateral – 24.77% (χ =5.35; p=0.021) or bilateral – 27.62% (χ =5.79; p=0.016). IMT---gt---0.9 mm was followed by a higher BP (p<0.001), FMD BA 11.80% decrease with compensatory increase in carotid arteries diameters – 17.38% and 21.99% (p<0.001) and sVCAM-1 by 20.49% (p=0.005). (rs2070744), but not (rs5443), gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and genes reduced transcription activity.
AbstractList The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to (rs5443) and (rs2070744) genes polymorphism in the essential arterial hypertension (EAH). Methods. One-hundred EAH patients (48 – control) participated in the case-control study. Soluble vascular cell adhesion molecule (sVCAM-1), total NO metabolites (NO +NO ), transcriptional activity of gene, endothelium-dependent flow-mediated dilation of the brachial artery (FMD BA), and carotid IMT were studied. (rs5443) and (rs2070744) genotyping was performed by TaqMan probes (CFX96™Real-Time PCR). Results. The connection of (rs2070744) with decreased total NO metabolites (F=71.11; p<0.001), reduced genes transcription activity (F=8.71; p<0.001) and increased sVCAM-1 (F=6.96; p=0.002), especially in the -allele carriers (particularly in -genotype patients with lower NO – 16.46% and 40.88%; p<0.001), lowered the transcription activity of NOS3 gene – 46.03% 7 times (p<0.001), and become higher sVCAM-1 – 35.48% and 89.48% (p<0.001), respectively. ANOVA did not confirm the association of (rs5443) gene with endothelial function and carotid IMT. Severe EAH was associated with increased carotid IMT – 50.0% (p<0.001) and 57.14% (p=0.007), wider carotid arteries – 17.36% (p=0.012) and 21.79% (p=0.004), and decreased NOS3 genes transcription activity – 34.54% (p=0.003). Atherosclerotic plaques were unilateral – 24.77% (χ =5.35; p=0.021) or bilateral – 27.62% (χ =5.79; p=0.016). IMT---gt---0.9 mm was followed by a higher BP (p<0.001), FMD BA 11.80% decrease with compensatory increase in carotid arteries diameters – 17.38% and 21.99% (p<0.001) and sVCAM-1 by 20.49% (p=0.005). (rs2070744), but not (rs5443), gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and genes reduced transcription activity.
Objective. The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to GNB3 (rs5443) and NOS3 (rs2070744) genes polymorphism in the essential arterial hypertension (EAH).
Abstract Objective. The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to GNB3 (rs5443) and NOS3 (rs2070744) genes polymorphism in the essential arterial hypertension (EAH). Methods. One-hundred EAH patients (48 – control) participated in the case-control study. Soluble vascular cell adhesion molecule (sVCAM-1), total NO metabolites (NO 2 – +NO 3 – ), transcriptional activity of NOS3 gene, endothelium-dependent flow-mediated dilation of the brachial artery (FMD BA), and carotid IMT were studied. GNB3 (rs5443) and NOS3 (rs2070744) genotyping was performed by TaqMan probes (CFX96™Real-Time PCR). Results. The connection of NOS3 (rs2070744) with decreased total NO metabolites (F=71.11; p<0.001), reduced NOS3 genes transcription activity (F=8.71; p<0.001) and increased sVCAM-1 (F=6.96; p=0.002), especially in the C -allele carriers (particularly in CC -genotype patients with lower NO – 16.46% and 40.88%; p<0.001), lowered the transcription activity of NOS3 gene – 46.03% 7 times (p<0.001), and become higher sVCAM-1 – 35.48% and 89.48% (p<0.001), respectively. ANOVA did not confirm the association of GNB3 (rs5443) gene with endothelial function and carotid IMT. Severe EAH was associated with increased carotid IMT – 50.0% (p<0.001) and 57.14% (p=0.007), wider carotid arteries – 17.36% (p=0.012) and 21.79% (p=0.004), and decreased NOS3 genes transcription activity – 34.54% (p=0.003). Atherosclerotic plaques were unilateral – 24.77% (χ 2 =5.35; p=0.021) or bilateral – 27.62% (χ 2 =5.79; p=0.016). IMT---gt---0.9 mm was followed by a higher BP (p<0.001), FMD BA 11.80% decrease with compensatory increase in carotid arteries diameters – 17.38% and 21.99% (p<0.001) and sVCAM-1 by 20.49% (p=0.005). Conclusion. NOS3 (rs2070744), but not GNB3 (rs5443), gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and NOS3 genes reduced transcription activity.
The aim of the present study was to clarify the endothelial function biomarkers and carotid "intima media" thickness (IMT) changes in relation to (rs5443) and (rs2070744) genes polymorphism in the essential arterial hypertension (EAH). Methods. One-hundred EAH patients (48 - control) participated in the case-control study. Soluble vascular cell adhesion molecule (sVCAM-1), total NO metabolites (NO +NO ), transcriptional activity of gene, endothelium-dependent flow-mediated dilation of the brachial artery (FMD BA), and carotid IMT were studied. (rs5443) and (rs2070744) genotyping was performed by TaqMan probes (CFX96™Real-Time PCR). Results. The connection of (rs2070744) with decreased total NO metabolites (F=71.11; p<0.001), reduced genes transcription activity (F=8.71; p<0.001) and increased sVCAM-1 (F=6.96; p=0.002), especially in the -allele carriers (particularly in -genotype patients with lower NO - 16.46% and 40.88%; p<0.001), lowered the transcription activity of NOS3 gene - 46.03% 7 times (p<0.001), and become higher sVCAM-1 - 35.48% and 89.48% (p<0.001), respectively. ANOVA did not confirm the association of (rs5443) gene with endothelial function and carotid IMT. Severe EAH was associated with increased carotid IMT - 50.0% (p<0.001) and 57.14% (p=0.007), wider carotid arteries - 17.36% (p=0.012) and 21.79% (p=0.004), and decreased NOS3 genes transcription activity - 34.54% (p=0.003). Atherosclerotic plaques were unilateral - 24.77% (χ =5.35; p=0.021) or bilateral - 27.62% (χ =5.79; p=0.016). IMT---gt---0.9 mm was followed by a higher BP (p<0.001), FMD BA 11.80% decrease with compensatory increase in carotid arteries diameters - 17.38% and 21.99% (p<0.001) and sVCAM-1 by 20.49% (p=0.005). (rs2070744), but not (rs5443), gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and genes reduced transcription activity.
Author Iftoda, Oksana M.
Gutnitska, Adelina F.
Sydorchuk, Larysa P.
Sydorchuk, Andrii R.
Ursuliak, Yulia V.
Dzhuryak, Valentina S.
Kryvetska, Inna I.
Sydorchuk, Ruslan I.
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Keywords but not GNB3 (rs5443)
NOS3 (rs2070744)
gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and NOS3 genes reduced transcription activity
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– ident: 2024042809421822176_j_enr-2022-0012_ref_025
– ident: 2024042809421822176_j_enr-2022-0012_ref_026
  doi: 10.1007/s11906-011-0238-3
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Snippet The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to (rs5443) and...
The aim of the present study was to clarify the endothelial function biomarkers and carotid "intima media" thickness (IMT) changes in relation to (rs5443) and...
Abstract Objective. The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in...
Objective. The aim of the present study was to clarify the endothelial function biomarkers and carotid “intima media” thickness (IMT) changes in relation to...
SourceID doaj
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walterdegruyter
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SubjectTerms Biomarkers
but not
but not gnb3 (rs5443)
Carotid Intima-Media Thickness
Case-Control Studies
Endothelium, Vascular
gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and
gene associated with the essential arterial hypertension severity relying upon the endothelial function impairment and nos3 genes reduced transcription activity
genes reduced transcription activity
Humans
Hypertension
Nitric Oxide Synthase Type III - genetics
nos3 (rs2070744)
rs2070744
rs5443
Title Endothelium function biomarkers and carotid intima-media thickness changes in relation to NOS3 (rs2070744) and GNB3 (rs5443) genes polymorphism in the essential arterial hypertension
URI http://www.degruyter.com/doi/10.2478/enr-2022-0012
https://www.ncbi.nlm.nih.gov/pubmed/35489051
https://search.proquest.com/docview/2658229106
https://doaj.org/article/a0242202e69f454ca1949a9113efb4a6
Volume 56
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