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Non-O-blood types associated with higher risk of high-grade atrioventricular block
INTRODUCTION: The non-O phenotype of the ABO genotype has been linked with an increased risk of cardiovascular disease. Atrioventricular (AV) block (AVB) is defined as retardation or cessation in the route of an electrical impulse passing from the atria to the ventricles because of an anatomical or...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900742/ https://www.ncbi.nlm.nih.gov/pubmed/31824992 http://dx.doi.org/10.5114/amsad.2019.90072 |
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author | Acar, Emrah İzci, Servet Inanir, Mehmet Yılmaz, Mehmet Fatih Kılıçgedik, Alev Güler, Yeliz Izgi, Ibrahim Akin Kirma, Cevat |
author_facet | Acar, Emrah İzci, Servet Inanir, Mehmet Yılmaz, Mehmet Fatih Kılıçgedik, Alev Güler, Yeliz Izgi, Ibrahim Akin Kirma, Cevat |
author_sort | Acar, Emrah |
collection | PubMed |
description | INTRODUCTION: The non-O phenotype of the ABO genotype has been linked with an increased risk of cardiovascular disease. Atrioventricular (AV) block (AVB) is defined as retardation or cessation in the route of an electrical impulse passing from the atria to the ventricles because of an anatomical or functional disruption in the conduction system. We aimed to interpret the association between blood group status and high-grade atrioventricular block (HAVB). MATERIAL AND METHODS: This study was implemented as a retrospective review of the recorded data of patients diagnosed with high-grade AV block and a control group. The study population consisted of 640 patients with HAVB and 570 control subjects. RESULTS: Presence of non-O blood group (p < 0.001) was significantly more prevalent in HAVB patients than in the control subjects. Blood group type was the sole independent predictor of HAVB in multiple regression analysis (p < 0.001, OR = 1.35, 95% CI: 1.08–1.57). Also, third-degree AVB had a higher incidence in the non-O blood subgroup and also non-O blood group was a predictor of third-degree AVB (p < 0.001, OR = 1.39, 95% CI: 1.13–1.69). The incidence of HAVB did not distinguish between the two Rh (D) groups. Rh (D) status did not have an impact on HAVB. CONCLUSIONS: This is the first study that has evaluated the potential relationship between HAVB and ABO blood groups. The main finding of this report is that patients with non-O blood group types have a higher risk for development of HAVB compared with O blood group patients. |
format | Online Article Text |
id | pubmed-6900742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-69007422019-12-10 Non-O-blood types associated with higher risk of high-grade atrioventricular block Acar, Emrah İzci, Servet Inanir, Mehmet Yılmaz, Mehmet Fatih Kılıçgedik, Alev Güler, Yeliz Izgi, Ibrahim Akin Kirma, Cevat Arch Med Sci Atheroscler Dis Clinical Research INTRODUCTION: The non-O phenotype of the ABO genotype has been linked with an increased risk of cardiovascular disease. Atrioventricular (AV) block (AVB) is defined as retardation or cessation in the route of an electrical impulse passing from the atria to the ventricles because of an anatomical or functional disruption in the conduction system. We aimed to interpret the association between blood group status and high-grade atrioventricular block (HAVB). MATERIAL AND METHODS: This study was implemented as a retrospective review of the recorded data of patients diagnosed with high-grade AV block and a control group. The study population consisted of 640 patients with HAVB and 570 control subjects. RESULTS: Presence of non-O blood group (p < 0.001) was significantly more prevalent in HAVB patients than in the control subjects. Blood group type was the sole independent predictor of HAVB in multiple regression analysis (p < 0.001, OR = 1.35, 95% CI: 1.08–1.57). Also, third-degree AVB had a higher incidence in the non-O blood subgroup and also non-O blood group was a predictor of third-degree AVB (p < 0.001, OR = 1.39, 95% CI: 1.13–1.69). The incidence of HAVB did not distinguish between the two Rh (D) groups. Rh (D) status did not have an impact on HAVB. CONCLUSIONS: This is the first study that has evaluated the potential relationship between HAVB and ABO blood groups. The main finding of this report is that patients with non-O blood group types have a higher risk for development of HAVB compared with O blood group patients. Termedia Publishing House 2019-11-26 /pmc/articles/PMC6900742/ /pubmed/31824992 http://dx.doi.org/10.5114/amsad.2019.90072 Text en Copyright: © 2019 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Acar, Emrah İzci, Servet Inanir, Mehmet Yılmaz, Mehmet Fatih Kılıçgedik, Alev Güler, Yeliz Izgi, Ibrahim Akin Kirma, Cevat Non-O-blood types associated with higher risk of high-grade atrioventricular block |
title | Non-O-blood types associated with higher risk of high-grade atrioventricular block |
title_full | Non-O-blood types associated with higher risk of high-grade atrioventricular block |
title_fullStr | Non-O-blood types associated with higher risk of high-grade atrioventricular block |
title_full_unstemmed | Non-O-blood types associated with higher risk of high-grade atrioventricular block |
title_short | Non-O-blood types associated with higher risk of high-grade atrioventricular block |
title_sort | non-o-blood types associated with higher risk of high-grade atrioventricular block |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900742/ https://www.ncbi.nlm.nih.gov/pubmed/31824992 http://dx.doi.org/10.5114/amsad.2019.90072 |
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