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Association of ABO blood group type with cardiovascular events in COVID-19
Cardiovascular complications have been reported in patients with COVID-19. We sought to examine the association of ABO blood group type with cardiovascular complications in COVID-19. We examined 409 individuals enrolled in the COVID-19 Registry to Assess Frequency, Management, and Outcomes of Arteri...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810281/ https://www.ncbi.nlm.nih.gov/pubmed/33452583 http://dx.doi.org/10.1007/s11239-020-02364-5 |
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author | Nauffal, Victor Achanta, Aditya Goldhaber, Samuel Z. Piazza, Gregory |
author_facet | Nauffal, Victor Achanta, Aditya Goldhaber, Samuel Z. Piazza, Gregory |
author_sort | Nauffal, Victor |
collection | PubMed |
description | Cardiovascular complications have been reported in patients with COVID-19. We sought to examine the association of ABO blood group type with cardiovascular complications in COVID-19. We examined 409 individuals enrolled in the COVID-19 Registry to Assess Frequency, Management, and Outcomes of Arterial and Venous Thromboembolic Complications (CORONA-VTE) who had ABO blood group data available. Multiple logistic regression was used to assess the association of ABO blood group types with three primary outcomes: major adverse cardiovascular events (MACE), major arterial and venous thrombosis and all-cause mortality. 201, 121, 61 and 26 individuals had blood group O, A, B and AB, respectively. In multivariable analysis, blood group A was associated with a 2.5-fold higher odds of MACE than blood group O (OR 2.47[1.18–5.18]). There was an effect suggesting a 2-fold higher odds of major thrombotic events in blood group A vs. O that did not reach statistical significance (OR 2.15 [0.89–5.20]). No association between blood group type and all-cause mortality was found. Compared with the other blood group types, blood group A was associated with an increased odds of MACE(OR(A/non−A) 2.18[1.11–4.29]), while blood group O was associated with lower odds of MACE(OR(O/non−O) 0.50[0.26–0.97]). In conclusion, blood group A was associated with an increased odds of MACE, whereas blood group O was associated with a reduction in the odds of MACE in patients with COVID-19. These findings may inform risk stratification of COVID-19 patients for cardiovascular complications. Additional studies are needed to validate our findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11239-020-02364-5. |
format | Online Article Text |
id | pubmed-7810281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-78102812021-01-18 Association of ABO blood group type with cardiovascular events in COVID-19 Nauffal, Victor Achanta, Aditya Goldhaber, Samuel Z. Piazza, Gregory J Thromb Thrombolysis Article Cardiovascular complications have been reported in patients with COVID-19. We sought to examine the association of ABO blood group type with cardiovascular complications in COVID-19. We examined 409 individuals enrolled in the COVID-19 Registry to Assess Frequency, Management, and Outcomes of Arterial and Venous Thromboembolic Complications (CORONA-VTE) who had ABO blood group data available. Multiple logistic regression was used to assess the association of ABO blood group types with three primary outcomes: major adverse cardiovascular events (MACE), major arterial and venous thrombosis and all-cause mortality. 201, 121, 61 and 26 individuals had blood group O, A, B and AB, respectively. In multivariable analysis, blood group A was associated with a 2.5-fold higher odds of MACE than blood group O (OR 2.47[1.18–5.18]). There was an effect suggesting a 2-fold higher odds of major thrombotic events in blood group A vs. O that did not reach statistical significance (OR 2.15 [0.89–5.20]). No association between blood group type and all-cause mortality was found. Compared with the other blood group types, blood group A was associated with an increased odds of MACE(OR(A/non−A) 2.18[1.11–4.29]), while blood group O was associated with lower odds of MACE(OR(O/non−O) 0.50[0.26–0.97]). In conclusion, blood group A was associated with an increased odds of MACE, whereas blood group O was associated with a reduction in the odds of MACE in patients with COVID-19. These findings may inform risk stratification of COVID-19 patients for cardiovascular complications. Additional studies are needed to validate our findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11239-020-02364-5. Springer US 2021-01-15 2021 /pmc/articles/PMC7810281/ /pubmed/33452583 http://dx.doi.org/10.1007/s11239-020-02364-5 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Nauffal, Victor Achanta, Aditya Goldhaber, Samuel Z. Piazza, Gregory Association of ABO blood group type with cardiovascular events in COVID-19 |
title | Association of ABO blood group type with cardiovascular events in COVID-19 |
title_full | Association of ABO blood group type with cardiovascular events in COVID-19 |
title_fullStr | Association of ABO blood group type with cardiovascular events in COVID-19 |
title_full_unstemmed | Association of ABO blood group type with cardiovascular events in COVID-19 |
title_short | Association of ABO blood group type with cardiovascular events in COVID-19 |
title_sort | association of abo blood group type with cardiovascular events in covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7810281/ https://www.ncbi.nlm.nih.gov/pubmed/33452583 http://dx.doi.org/10.1007/s11239-020-02364-5 |
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