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Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey

BACKGROUND: Health conditions, immune dysfunction, and premature aging associated with trisomy 21 (Down syndrome, DS) may impact the clinical course of COVID-19. METHODS: The T21RS COVID-19 Initiative launched an international survey for clinicians or caregivers on patients with COVID-19 and DS. Dat...

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Autores principales: Hüls, Anke, Costa, Alberto C.S., Dierssen, Mara, Baksh, R. Asaad, Bargagna, Stefania, Baumer, Nicole T., Brandão, Ana Claudia, Carfi, Angelo, Carmona-Iragui, Maria, Chicoine, Brian Allen, Ghosh, Sujay, Lakhanpaul, Monica, Manso, Coral, Mayer, Miguel-Angel, Ortega, Maria del Carmen, de Asua, Diego Real, Rebillat, Anne-Sophie, Russell, Lauren Ashley, Sgandurra, Giuseppina, Valentini, Diletta, Sherman, Stephanie L., Strydom, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897934/
https://www.ncbi.nlm.nih.gov/pubmed/33644721
http://dx.doi.org/10.1016/j.eclinm.2021.100769
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author Hüls, Anke
Costa, Alberto C.S.
Dierssen, Mara
Baksh, R. Asaad
Bargagna, Stefania
Baumer, Nicole T.
Brandão, Ana Claudia
Carfi, Angelo
Carmona-Iragui, Maria
Chicoine, Brian Allen
Ghosh, Sujay
Lakhanpaul, Monica
Manso, Coral
Mayer, Miguel-Angel
Ortega, Maria del Carmen
de Asua, Diego Real
Rebillat, Anne-Sophie
Russell, Lauren Ashley
Sgandurra, Giuseppina
Valentini, Diletta
Sherman, Stephanie L.
Strydom, Andre
author_facet Hüls, Anke
Costa, Alberto C.S.
Dierssen, Mara
Baksh, R. Asaad
Bargagna, Stefania
Baumer, Nicole T.
Brandão, Ana Claudia
Carfi, Angelo
Carmona-Iragui, Maria
Chicoine, Brian Allen
Ghosh, Sujay
Lakhanpaul, Monica
Manso, Coral
Mayer, Miguel-Angel
Ortega, Maria del Carmen
de Asua, Diego Real
Rebillat, Anne-Sophie
Russell, Lauren Ashley
Sgandurra, Giuseppina
Valentini, Diletta
Sherman, Stephanie L.
Strydom, Andre
author_sort Hüls, Anke
collection PubMed
description BACKGROUND: Health conditions, immune dysfunction, and premature aging associated with trisomy 21 (Down syndrome, DS) may impact the clinical course of COVID-19. METHODS: The T21RS COVID-19 Initiative launched an international survey for clinicians or caregivers on patients with COVID-19 and DS. Data collected between April and October 2020 (N=1046) were analysed and compared with the UK ISARIC4C survey of hospitalized COVID-19 patients with and without DS. FINDINGS: The mean age of COVID-19 patients with DS in the T21RS survey was 29 years (SD = 18). Similar to the general population, the most frequent signs and symptoms of COVID-19 were fever, cough, and shortness of breath. Joint/muscle pain and vomiting or nausea were less frequent (p < 0.01), whereas altered consciousness/confusion were more frequent (p < 0.01). Risk factors for hospitalization and mortality were similar to the general population with the addition of congenital heart defects as a risk factor for hospitalization. Mortality rates showed a rapid increase from age 40 and were higher in patients with DS (T21RS DS versus non-DS patients: risk ratio (RR) = 3.5 (95%-CI=2.6;4.4), ISARIC4C DS versus non-DS patients: RR = 2.9 (95%-CI=2.1;3.8)) even after adjusting for known risk factors for COVID-19 mortality. INTERPRETATION: Leading signs/symptoms of COVID-19 and risk factors for severe disease course are similar to the general population. However, individuals with DS present significantly higher rates of medical complications and mortality, especially from age 40. FUNDING: Down Syndrome Affiliates in Action, DSMIG-USA, GiGi's Playhouse, Jerome Lejeune Foundation, LuMind IDSC Foundation, The Matthew Foundation, NDSS, National Task Group on Intellectual Disabilities and Dementia Practices.
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spelling pubmed-78979342021-02-22 Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey Hüls, Anke Costa, Alberto C.S. Dierssen, Mara Baksh, R. Asaad Bargagna, Stefania Baumer, Nicole T. Brandão, Ana Claudia Carfi, Angelo Carmona-Iragui, Maria Chicoine, Brian Allen Ghosh, Sujay Lakhanpaul, Monica Manso, Coral Mayer, Miguel-Angel Ortega, Maria del Carmen de Asua, Diego Real Rebillat, Anne-Sophie Russell, Lauren Ashley Sgandurra, Giuseppina Valentini, Diletta Sherman, Stephanie L. Strydom, Andre EClinicalMedicine Research Paper BACKGROUND: Health conditions, immune dysfunction, and premature aging associated with trisomy 21 (Down syndrome, DS) may impact the clinical course of COVID-19. METHODS: The T21RS COVID-19 Initiative launched an international survey for clinicians or caregivers on patients with COVID-19 and DS. Data collected between April and October 2020 (N=1046) were analysed and compared with the UK ISARIC4C survey of hospitalized COVID-19 patients with and without DS. FINDINGS: The mean age of COVID-19 patients with DS in the T21RS survey was 29 years (SD = 18). Similar to the general population, the most frequent signs and symptoms of COVID-19 were fever, cough, and shortness of breath. Joint/muscle pain and vomiting or nausea were less frequent (p < 0.01), whereas altered consciousness/confusion were more frequent (p < 0.01). Risk factors for hospitalization and mortality were similar to the general population with the addition of congenital heart defects as a risk factor for hospitalization. Mortality rates showed a rapid increase from age 40 and were higher in patients with DS (T21RS DS versus non-DS patients: risk ratio (RR) = 3.5 (95%-CI=2.6;4.4), ISARIC4C DS versus non-DS patients: RR = 2.9 (95%-CI=2.1;3.8)) even after adjusting for known risk factors for COVID-19 mortality. INTERPRETATION: Leading signs/symptoms of COVID-19 and risk factors for severe disease course are similar to the general population. However, individuals with DS present significantly higher rates of medical complications and mortality, especially from age 40. FUNDING: Down Syndrome Affiliates in Action, DSMIG-USA, GiGi's Playhouse, Jerome Lejeune Foundation, LuMind IDSC Foundation, The Matthew Foundation, NDSS, National Task Group on Intellectual Disabilities and Dementia Practices. Elsevier 2021-02-22 /pmc/articles/PMC7897934/ /pubmed/33644721 http://dx.doi.org/10.1016/j.eclinm.2021.100769 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Hüls, Anke
Costa, Alberto C.S.
Dierssen, Mara
Baksh, R. Asaad
Bargagna, Stefania
Baumer, Nicole T.
Brandão, Ana Claudia
Carfi, Angelo
Carmona-Iragui, Maria
Chicoine, Brian Allen
Ghosh, Sujay
Lakhanpaul, Monica
Manso, Coral
Mayer, Miguel-Angel
Ortega, Maria del Carmen
de Asua, Diego Real
Rebillat, Anne-Sophie
Russell, Lauren Ashley
Sgandurra, Giuseppina
Valentini, Diletta
Sherman, Stephanie L.
Strydom, Andre
Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey
title Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey
title_full Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey
title_fullStr Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey
title_full_unstemmed Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey
title_short Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey
title_sort medical vulnerability of individuals with down syndrome to severe covid-19–data from the trisomy 21 research society and the uk isaric4c survey
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897934/
https://www.ncbi.nlm.nih.gov/pubmed/33644721
http://dx.doi.org/10.1016/j.eclinm.2021.100769
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