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SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study

BACKGROUND: SARS-CoV-2 lineage B.1.1.7 has been associated with an increased rate of transmission and disease severity among subjects testing positive in the community. Its impact on hospitalised patients is less well documented. METHODS: We collected viral sequences and clinical data of patients ad...

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Autores principales: Stirrup, Oliver, Boshier, Florencia, Venturini, Cristina, Guerra-Assunção, José Afonso, Alcolea-Medina, Adela, Beckett, Angela, Charalampous, Themoula, da Silva Filipe, Ana, Glaysher, Sharon, Khan, Tabassum, Kulasegaran Shylini, Raghavendran, Kele, Beatrix, Monahan, Irene, Mollett, Guy, Parker, Matthew, Pelosi, Emanuela, Randell, Paul, Roy, Sunando, Taylor, Joshua, Weller, Sophie, Wilson-Davies, Eleri, Wade, Phillip, Williams, Rachel, Copas, Andrew, Cutino-Moguel, Maria-Teresa, Freemantle, Nick, Hayward, Andrew C, Holmes, Alison, Hughes, Joseph, Mahungu, Tabitha, Nebbia, Gaia, Partridge, David, Pope, Cassie, Price, James, Robson, Samuel, Saeed, Kordo, de Silva, Thushan, Snell, Luke, Thomson, Emma, Witney, Adam A, Breuer, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453594/
https://www.ncbi.nlm.nih.gov/pubmed/34544733
http://dx.doi.org/10.1136/bmjresp-2021-001029
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author Stirrup, Oliver
Boshier, Florencia
Venturini, Cristina
Guerra-Assunção, José Afonso
Alcolea-Medina, Adela
Beckett, Angela
Charalampous, Themoula
da Silva Filipe, Ana
Glaysher, Sharon
Khan, Tabassum
Kulasegaran Shylini, Raghavendran
Kele, Beatrix
Monahan, Irene
Mollett, Guy
Parker, Matthew
Pelosi, Emanuela
Randell, Paul
Roy, Sunando
Taylor, Joshua
Weller, Sophie
Wilson-Davies, Eleri
Wade, Phillip
Williams, Rachel
Copas, Andrew
Cutino-Moguel, Maria-Teresa
Freemantle, Nick
Hayward, Andrew C
Holmes, Alison
Hughes, Joseph
Mahungu, Tabitha
Nebbia, Gaia
Partridge, David
Pope, Cassie
Price, James
Robson, Samuel
Saeed, Kordo
de Silva, Thushan
Snell, Luke
Thomson, Emma
Witney, Adam A
Breuer, Judith
author_facet Stirrup, Oliver
Boshier, Florencia
Venturini, Cristina
Guerra-Assunção, José Afonso
Alcolea-Medina, Adela
Beckett, Angela
Charalampous, Themoula
da Silva Filipe, Ana
Glaysher, Sharon
Khan, Tabassum
Kulasegaran Shylini, Raghavendran
Kele, Beatrix
Monahan, Irene
Mollett, Guy
Parker, Matthew
Pelosi, Emanuela
Randell, Paul
Roy, Sunando
Taylor, Joshua
Weller, Sophie
Wilson-Davies, Eleri
Wade, Phillip
Williams, Rachel
Copas, Andrew
Cutino-Moguel, Maria-Teresa
Freemantle, Nick
Hayward, Andrew C
Holmes, Alison
Hughes, Joseph
Mahungu, Tabitha
Nebbia, Gaia
Partridge, David
Pope, Cassie
Price, James
Robson, Samuel
Saeed, Kordo
de Silva, Thushan
Snell, Luke
Thomson, Emma
Witney, Adam A
Breuer, Judith
author_sort Stirrup, Oliver
collection PubMed
description BACKGROUND: SARS-CoV-2 lineage B.1.1.7 has been associated with an increased rate of transmission and disease severity among subjects testing positive in the community. Its impact on hospitalised patients is less well documented. METHODS: We collected viral sequences and clinical data of patients admitted with SARS-CoV-2 and hospital-onset COVID-19 infections (HOCIs), sampled 16 November 2020 to 10 January 2021, from eight hospitals participating in the COG-UK-HOCI study. Associations between the variant and the outcomes of all-cause mortality and intensive therapy unit (ITU) admission were evaluated using mixed effects Cox models adjusted by age, sex, comorbidities, care home residence, pregnancy and ethnicity. FINDINGS: Sequences were obtained from 2341 inpatients (HOCI cases=786) and analysis of clinical outcomes was carried out in 2147 inpatients with all data available. The HR for mortality of B.1.1.7 compared with other lineages was 1.01 (95% CI 0.79 to 1.28, p=0.94) and for ITU admission was 1.01 (95% CI 0.75 to 1.37, p=0.96). Analysis of sex-specific effects of B.1.1.7 identified increased risk of mortality (HR 1.30, 95% CI 0.95 to 1.78, p=0.096) and ITU admission (HR 1.82, 95% CI 1.15 to 2.90, p=0.011) in females infected with the variant but not males (mortality HR 0.82, 95% CI 0.61 to 1.10, p=0.177; ITU HR 0.74, 95% CI 0.52 to 1.04, p=0.086). INTERPRETATION: In common with smaller studies of patients hospitalised with SARS-CoV-2, we did not find an overall increase in mortality or ITU admission associated with B.1.1.7 compared with other lineages. However, women with B.1.1.7 may be at an increased risk of admission to intensive care and at modestly increased risk of mortality.
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spelling pubmed-84535942021-09-22 SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study Stirrup, Oliver Boshier, Florencia Venturini, Cristina Guerra-Assunção, José Afonso Alcolea-Medina, Adela Beckett, Angela Charalampous, Themoula da Silva Filipe, Ana Glaysher, Sharon Khan, Tabassum Kulasegaran Shylini, Raghavendran Kele, Beatrix Monahan, Irene Mollett, Guy Parker, Matthew Pelosi, Emanuela Randell, Paul Roy, Sunando Taylor, Joshua Weller, Sophie Wilson-Davies, Eleri Wade, Phillip Williams, Rachel Copas, Andrew Cutino-Moguel, Maria-Teresa Freemantle, Nick Hayward, Andrew C Holmes, Alison Hughes, Joseph Mahungu, Tabitha Nebbia, Gaia Partridge, David Pope, Cassie Price, James Robson, Samuel Saeed, Kordo de Silva, Thushan Snell, Luke Thomson, Emma Witney, Adam A Breuer, Judith BMJ Open Respir Res Respiratory Infection BACKGROUND: SARS-CoV-2 lineage B.1.1.7 has been associated with an increased rate of transmission and disease severity among subjects testing positive in the community. Its impact on hospitalised patients is less well documented. METHODS: We collected viral sequences and clinical data of patients admitted with SARS-CoV-2 and hospital-onset COVID-19 infections (HOCIs), sampled 16 November 2020 to 10 January 2021, from eight hospitals participating in the COG-UK-HOCI study. Associations between the variant and the outcomes of all-cause mortality and intensive therapy unit (ITU) admission were evaluated using mixed effects Cox models adjusted by age, sex, comorbidities, care home residence, pregnancy and ethnicity. FINDINGS: Sequences were obtained from 2341 inpatients (HOCI cases=786) and analysis of clinical outcomes was carried out in 2147 inpatients with all data available. The HR for mortality of B.1.1.7 compared with other lineages was 1.01 (95% CI 0.79 to 1.28, p=0.94) and for ITU admission was 1.01 (95% CI 0.75 to 1.37, p=0.96). Analysis of sex-specific effects of B.1.1.7 identified increased risk of mortality (HR 1.30, 95% CI 0.95 to 1.78, p=0.096) and ITU admission (HR 1.82, 95% CI 1.15 to 2.90, p=0.011) in females infected with the variant but not males (mortality HR 0.82, 95% CI 0.61 to 1.10, p=0.177; ITU HR 0.74, 95% CI 0.52 to 1.04, p=0.086). INTERPRETATION: In common with smaller studies of patients hospitalised with SARS-CoV-2, we did not find an overall increase in mortality or ITU admission associated with B.1.1.7 compared with other lineages. However, women with B.1.1.7 may be at an increased risk of admission to intensive care and at modestly increased risk of mortality. BMJ Publishing Group 2021-09-20 /pmc/articles/PMC8453594/ /pubmed/34544733 http://dx.doi.org/10.1136/bmjresp-2021-001029 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Respiratory Infection
Stirrup, Oliver
Boshier, Florencia
Venturini, Cristina
Guerra-Assunção, José Afonso
Alcolea-Medina, Adela
Beckett, Angela
Charalampous, Themoula
da Silva Filipe, Ana
Glaysher, Sharon
Khan, Tabassum
Kulasegaran Shylini, Raghavendran
Kele, Beatrix
Monahan, Irene
Mollett, Guy
Parker, Matthew
Pelosi, Emanuela
Randell, Paul
Roy, Sunando
Taylor, Joshua
Weller, Sophie
Wilson-Davies, Eleri
Wade, Phillip
Williams, Rachel
Copas, Andrew
Cutino-Moguel, Maria-Teresa
Freemantle, Nick
Hayward, Andrew C
Holmes, Alison
Hughes, Joseph
Mahungu, Tabitha
Nebbia, Gaia
Partridge, David
Pope, Cassie
Price, James
Robson, Samuel
Saeed, Kordo
de Silva, Thushan
Snell, Luke
Thomson, Emma
Witney, Adam A
Breuer, Judith
SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
title SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
title_full SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
title_fullStr SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
title_full_unstemmed SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
title_short SARS-CoV-2 lineage B.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
title_sort sars-cov-2 lineage b.1.1.7 is associated with greater disease severity among hospitalised women but not men: multicentre cohort study
topic Respiratory Infection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453594/
https://www.ncbi.nlm.nih.gov/pubmed/34544733
http://dx.doi.org/10.1136/bmjresp-2021-001029
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