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Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race

Prior literature has established a positive association between sickle cell disease and risk of contracting SARS-CoV-2. Data from a cross-sectional study evaluating COVID-19 testing devices (n = 10,567) was used to examine the association between underlying health conditions and SARS-CoV-2 infection...

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Autores principales: Frediani, Jennifer K., Pak-Harvey, Ezra, Parsons, Richard, Westbrook, Adrianna L., O'Sick, William, Martin, Greg S., Lam, Wilbur A., Levy, Joshua M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198733/
https://www.ncbi.nlm.nih.gov/pubmed/37257234
http://dx.doi.org/10.1016/j.bcmd.2023.102756
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author Frediani, Jennifer K.
Pak-Harvey, Ezra
Parsons, Richard
Westbrook, Adrianna L.
O'Sick, William
Martin, Greg S.
Lam, Wilbur A.
Levy, Joshua M.
author_facet Frediani, Jennifer K.
Pak-Harvey, Ezra
Parsons, Richard
Westbrook, Adrianna L.
O'Sick, William
Martin, Greg S.
Lam, Wilbur A.
Levy, Joshua M.
author_sort Frediani, Jennifer K.
collection PubMed
description Prior literature has established a positive association between sickle cell disease and risk of contracting SARS-CoV-2. Data from a cross-sectional study evaluating COVID-19 testing devices (n = 10,567) was used to examine the association between underlying health conditions and SARS-CoV-2 infection in an urban metropolis in the southern United States. Firth's logistic regression was used to fit the model predicting SARS-CoV-2 positivity using vaccine status and different medical conditions commonly associated with COVID-19. Another model using the same method was built using SARS-CoV-2 positivity as the outcome and hemoglobinopathy presence, age (<16 Years vs. ≥16 Years), race/ethnicity and comorbidities, including hemoglobinopathy, as the factors. Our first model showed a significant association between hemoglobinopathy and SARS-CoV-2 infection (OR: 2.28, 95 % CI: (1.17,4.35), P = 0.016). However, in the second model, this association was not maintained (OR: 1.35, 95 % CI: (0.72,2.50), P = 0.344). We conclude that the association between SARS-CoV-2 positivity and presence of hemoglobinopathies like sickle cell disease is confounded by race, age, and comorbidity status. Our results illuminate previous findings by identifying underlying clinical/demographic factors that confound the reported association between hemoglobinopathies and SARS-CoV-2. These findings demonstrate how social determinants of health may influence disease manifestations more than genetics alone.
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spelling pubmed-101987332023-05-22 Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race Frediani, Jennifer K. Pak-Harvey, Ezra Parsons, Richard Westbrook, Adrianna L. O'Sick, William Martin, Greg S. Lam, Wilbur A. Levy, Joshua M. Blood Cells Mol Dis Short Communication Prior literature has established a positive association between sickle cell disease and risk of contracting SARS-CoV-2. Data from a cross-sectional study evaluating COVID-19 testing devices (n = 10,567) was used to examine the association between underlying health conditions and SARS-CoV-2 infection in an urban metropolis in the southern United States. Firth's logistic regression was used to fit the model predicting SARS-CoV-2 positivity using vaccine status and different medical conditions commonly associated with COVID-19. Another model using the same method was built using SARS-CoV-2 positivity as the outcome and hemoglobinopathy presence, age (<16 Years vs. ≥16 Years), race/ethnicity and comorbidities, including hemoglobinopathy, as the factors. Our first model showed a significant association between hemoglobinopathy and SARS-CoV-2 infection (OR: 2.28, 95 % CI: (1.17,4.35), P = 0.016). However, in the second model, this association was not maintained (OR: 1.35, 95 % CI: (0.72,2.50), P = 0.344). We conclude that the association between SARS-CoV-2 positivity and presence of hemoglobinopathies like sickle cell disease is confounded by race, age, and comorbidity status. Our results illuminate previous findings by identifying underlying clinical/demographic factors that confound the reported association between hemoglobinopathies and SARS-CoV-2. These findings demonstrate how social determinants of health may influence disease manifestations more than genetics alone. Elsevier Inc. 2023-09 2023-05-19 /pmc/articles/PMC10198733/ /pubmed/37257234 http://dx.doi.org/10.1016/j.bcmd.2023.102756 Text en © 2023 Elsevier Inc. 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 Short Communication
Frediani, Jennifer K.
Pak-Harvey, Ezra
Parsons, Richard
Westbrook, Adrianna L.
O'Sick, William
Martin, Greg S.
Lam, Wilbur A.
Levy, Joshua M.
Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race
title Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race
title_full Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race
title_fullStr Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race
title_full_unstemmed Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race
title_short Prevalence of SARS-CoV-2 in hemoglobinopathies is modified by age and race
title_sort prevalence of sars-cov-2 in hemoglobinopathies is modified by age and race
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198733/
https://www.ncbi.nlm.nih.gov/pubmed/37257234
http://dx.doi.org/10.1016/j.bcmd.2023.102756
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