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Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2()
BACKGROUND AND OBJECTIVES: In the pandemic caused by SARS-CoV-2, identifying which risk factors are associated with the most serious forms of the disease is important. Blood group A has been presented in various studies as a poor prognostic factor. The objective of this study was to evaluate whether...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier España, S.L.U.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240948/ https://www.ncbi.nlm.nih.gov/pubmed/35784826 http://dx.doi.org/10.1016/j.medcle.2021.06.028 |
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author | Tamayo-Velasco, Álvaro Jiménez García, María Teresa Sanchez Rodríguez, Alba Hijas Villaizan, Milagros Carretero Gómez, Juana Miramontes-González, José Pablo |
author_facet | Tamayo-Velasco, Álvaro Jiménez García, María Teresa Sanchez Rodríguez, Alba Hijas Villaizan, Milagros Carretero Gómez, Juana Miramontes-González, José Pablo |
author_sort | Tamayo-Velasco, Álvaro |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: In the pandemic caused by SARS-CoV-2, identifying which risk factors are associated with the most serious forms of the disease is important. Blood group A has been presented in various studies as a poor prognostic factor. The objective of this study was to evaluate whether patients with blood group A were associated with more important comorbidities, measured by the Charlson Index, which may explain their worse clinical evolution. PATIENTS AND METHODS: A prospective and consecutive study examined 100 patients diagnosed with COVID-19 and admitted in March 2020. A multivariate linear regression model was used to evaluate the association of blood group A with the Charlson Index. RESULTS: Patients in group A had a higher Charlson Index (P = .037), rate of lymphopenia (P = .039) and thrombopenia (P = .014), and hospital mortality (P = .044). Blood group A was an independent factor associated with the Charlson Index (B 0.582, 95% CI 0.02–1.14, P = .041). CONCLUSIONS: Group A was independently associated with greater comorbidity, associated with an increase of 0.582 points in the Charlson Index compared to other blood groups. It was also associated with lower hospital mortality. |
format | Online Article Text |
id | pubmed-9240948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier España, S.L.U. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92409482022-06-29 Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() Tamayo-Velasco, Álvaro Jiménez García, María Teresa Sanchez Rodríguez, Alba Hijas Villaizan, Milagros Carretero Gómez, Juana Miramontes-González, José Pablo Med Clin (Engl Ed) Brief Report BACKGROUND AND OBJECTIVES: In the pandemic caused by SARS-CoV-2, identifying which risk factors are associated with the most serious forms of the disease is important. Blood group A has been presented in various studies as a poor prognostic factor. The objective of this study was to evaluate whether patients with blood group A were associated with more important comorbidities, measured by the Charlson Index, which may explain their worse clinical evolution. PATIENTS AND METHODS: A prospective and consecutive study examined 100 patients diagnosed with COVID-19 and admitted in March 2020. A multivariate linear regression model was used to evaluate the association of blood group A with the Charlson Index. RESULTS: Patients in group A had a higher Charlson Index (P = .037), rate of lymphopenia (P = .039) and thrombopenia (P = .014), and hospital mortality (P = .044). Blood group A was an independent factor associated with the Charlson Index (B 0.582, 95% CI 0.02–1.14, P = .041). CONCLUSIONS: Group A was independently associated with greater comorbidity, associated with an increase of 0.582 points in the Charlson Index compared to other blood groups. It was also associated with lower hospital mortality. Elsevier España, S.L.U. 2022-07-08 2022-06-29 /pmc/articles/PMC9240948/ /pubmed/35784826 http://dx.doi.org/10.1016/j.medcle.2021.06.028 Text en © 2021 Elsevier España, S.L.U. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Brief Report Tamayo-Velasco, Álvaro Jiménez García, María Teresa Sanchez Rodríguez, Alba Hijas Villaizan, Milagros Carretero Gómez, Juana Miramontes-González, José Pablo Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() |
title | Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() |
title_full | Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() |
title_fullStr | Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() |
title_full_unstemmed | Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() |
title_short | Association of blood group A with hospital comorbidity in patients infected by SARS-CoV-2() |
title_sort | association of blood group a with hospital comorbidity in patients infected by sars-cov-2() |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240948/ https://www.ncbi.nlm.nih.gov/pubmed/35784826 http://dx.doi.org/10.1016/j.medcle.2021.06.028 |
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