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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.
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.
  • Stirrup O; Institute for Global Health, University College London, London, UK oliver.stirrup@ucl.ac.uk.
  • Boshier F; Department of Infection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Venturini C; Department of Infection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Guerra-Assunção JA; Department of Infection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Alcolea-Medina A; Department of Genetics & Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Beckett A; Centre for Clinical Infection and Diagnostics Research, School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Charalampous T; Infection Sciences, Viapath, London, UK.
  • da Silva Filipe A; Centre for Enzyme Innovation, University of Portsmouth, Portsmouth, UK.
  • Glaysher S; School of Biological Sciences, University of Portsmouth, Portsmouth, UK.
  • Khan T; Centre for Clinical Infection and Diagnostics Research, School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Kulasegaran Shylini R; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Kele B; Portsmouth Hospitals University NHS Trust, Queen Alexandra Hospital, Portsmouth, UK.
  • Monahan I; Division of Infection, The Royal London Hospital, Barts Health NHS Trust, London, UK.
  • Mollett G; Division of Infection, The Royal London Hospital, Barts Health NHS Trust, London, UK.
  • Parker M; Division of Infection, The Royal London Hospital, Barts Health NHS Trust, London, UK.
  • Pelosi E; Institute for Infection and Immunity, St George's University of London, London, UK.
  • Randell P; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Roy S; Sheffield Bioinformatics Core, The University of Sheffield, Sheffield, UK.
  • Taylor J; Sheffield Institute for Translational Neuroscience, The University of Sheffield, Sheffield, UK.
  • Weller S; Sheffield Biomedical Research Centre, The University of Sheffield, Sheffield, UK.
  • Wilson-Davies E; Southampton Specialist Virology Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Wade P; Department of Infection and Immunity, North West London Pathology, London, UK.
  • Williams R; Department of Infection, Immunity and Inflammation, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Copas A; Southampton Specialist Virology Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Cutino-Moguel MT; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Freemantle N; The Florey Institute for Host-Pathogen Interactions & Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, Sheffield, UK.
  • Hayward AC; Department of Genetics & Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Mahungu T; Institute for Global Health, University College London, London, UK.
  • Nebbia G; Division of Infection, The Royal London Hospital, Barts Health NHS Trust, London, UK.
  • Partridge D; Institute of Clinical Trials and Methodology, University College London, London, UK.
  • Pope C; Institute of Epidemiology and Health Care, University College London, London, UK.
  • Price J; Department of Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Robson S; Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.
  • Saeed K; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • de Silva T; Department of Virology, Royal Free London NHS Foundation Trust, London, UK.
  • Snell L; Centre for Clinical Infection and Diagnostics Research, School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Thomson E; Department of Infectious Diseases, Guy's and St Thomas' Hospital NHS Foundation Trust, London, UK.
  • Witney AA; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Breuer J; The Florey Institute for Host-Pathogen Interactions & Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, Sheffield, UK.
BMJ Open Respir Res ; 8(1)2021 09.
Article in English | MEDLINE | ID: covidwho-1430193
ABSTRACT

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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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Variants Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Country/Region as subject: Europa Language: English Year: 2021 Document Type: Article Affiliation country: Bmjresp-2021-001029

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Variants Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Country/Region as subject: Europa Language: English Year: 2021 Document Type: Article Affiliation country: Bmjresp-2021-001029