open access

Vol 5, No 3 (2020)
Original article
Published online: 2020-09-07
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Soluble vascular cell adhesion molecule-1 in patients with non-valvular atrial fibrillation

Marzena Anaszewicz1, Joanna Wiśniewska1, Artur Mieczkowski1, Marcin Wasielewski1, Karol Suppan1, Beata Czerniak1, Kinga Lis2, Magdalena Żbikowska-Gotz2, Zbigniew Bartuzi2, Jacek Budzyński1
·
Medical Research Journal 2020;5(3):158-166.
Affiliations
  1. Department of Vascular and Internal Diseases, Faculty of Health Sciences, Ludwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Poland, 75 UjejskiegoStreet, 85-168 Bydgoszcz, Poland
  2. Department of Allergology, Clinical Immunology and Internal Diseases, Faculty of Medicine, Ludwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Poland, 75 Ujejskiego Street, 85-168 Bydgoszcz, Poland

open access

Vol 5, No 3 (2020)
ORIGINAL ARTICLES
Published online: 2020-09-07

Abstract

Background: Disturbances in atrial microcirculation is recognized as a risk factor for atrial fibrillation (AF).

Aim:
The aim of this study was to determine the associations between circulating soluble vascular cell adhesion molecule-1 (sVCAM-1) and the risk of AF and a one-year prognosis among consecutive inpatients.

Methods:
Eighty consecutive inpatients hospitalized due to non-valvular AF and 80 consecutive inpatients admitted for exacerbation of chronic coronary syndrome (control group) were enrolled in the study. A cardiologic workup was performed and blood sVCAM-1 concentration was determined using the ELISA method.

Results:
Patients with AF had similar blood sVCAM-1 concentration compared to the control group. AF patients treated with new oral anticoagulants (NOACs) were significantly less likely to have a sVCAM-1 concentration elevated above the median value than patients treated with warfarin (34.2% vs 65.8%; p = 0.01). Patients with an increased percentage of fat mass (FM) had lower sVCAM-1 concentration. The risk of all-cause mortality and MACE during follow-up rose in individuals with elevated sVCAM-1 (≥ 1242 and ≥ 587 ng/ml, respectively) with (OR; 95%CI): 5.39; 1.57-18.45; p = 0.007, and 6.00; 1.18-30.37; p = 0.03, respectively. Risk of death rose with increase in the ratio of sVCAM-1 and FM (1.02; 1.00-1.04; p = 0.019).

Conclusions:
Elevated sVCAM-1 was associated with all-cause mortality and MACE during one-year follow- up, but do not links the risk of AF. Use of NOACs may favorable affect endothelial function, A lower level of sVCAM-1 in obese patients may mediate the phenomenon of the “obesity paradox” in patients with AF.

Abstract

Background: Disturbances in atrial microcirculation is recognized as a risk factor for atrial fibrillation (AF).

Aim:
The aim of this study was to determine the associations between circulating soluble vascular cell adhesion molecule-1 (sVCAM-1) and the risk of AF and a one-year prognosis among consecutive inpatients.

Methods:
Eighty consecutive inpatients hospitalized due to non-valvular AF and 80 consecutive inpatients admitted for exacerbation of chronic coronary syndrome (control group) were enrolled in the study. A cardiologic workup was performed and blood sVCAM-1 concentration was determined using the ELISA method.

Results:
Patients with AF had similar blood sVCAM-1 concentration compared to the control group. AF patients treated with new oral anticoagulants (NOACs) were significantly less likely to have a sVCAM-1 concentration elevated above the median value than patients treated with warfarin (34.2% vs 65.8%; p = 0.01). Patients with an increased percentage of fat mass (FM) had lower sVCAM-1 concentration. The risk of all-cause mortality and MACE during follow-up rose in individuals with elevated sVCAM-1 (≥ 1242 and ≥ 587 ng/ml, respectively) with (OR; 95%CI): 5.39; 1.57-18.45; p = 0.007, and 6.00; 1.18-30.37; p = 0.03, respectively. Risk of death rose with increase in the ratio of sVCAM-1 and FM (1.02; 1.00-1.04; p = 0.019).

Conclusions:
Elevated sVCAM-1 was associated with all-cause mortality and MACE during one-year follow- up, but do not links the risk of AF. Use of NOACs may favorable affect endothelial function, A lower level of sVCAM-1 in obese patients may mediate the phenomenon of the “obesity paradox” in patients with AF.

Get Citation

Keywords

sVCAM-1; atrial fibrillation; thromboembolic complications; mortality, obesity paradox; new oral anticoagulants

About this article
Title

Soluble vascular cell adhesion molecule-1 in patients with non-valvular atrial fibrillation

Journal

Medical Research Journal

Issue

Vol 5, No 3 (2020)

Article type

Original article

Pages

158-166

Published online

2020-09-07

Page views

545

Article views/downloads

577

DOI

10.5603/MRJ.a2020.0032

Bibliographic record

Medical Research Journal 2020;5(3):158-166.

Keywords

sVCAM-1
atrial fibrillation
thromboembolic complications
mortality
obesity paradox
new oral anticoagulants

Authors

Marzena Anaszewicz
Joanna Wiśniewska
Artur Mieczkowski
Marcin Wasielewski
Karol Suppan
Beata Czerniak
Kinga Lis
Magdalena Żbikowska-Gotz
Zbigniew Bartuzi
Jacek Budzyński

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