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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

Authors :
Judith Breuer
Catherine F Houlihan
Nick Freemantle
David Partridge
Gaia Nebbia
Jacqui Prieto
Gee Yen Shin
Andrew Copas
Oliver Stirrup
Kenneth Laing
Rachel Williams
Helen Wheeler
Paul Randell
Ana da Silva Filipe
Maria-Teresa Cutino-Moguel
Tommy Rampling
Tabassum Khan
James Price
Eleni Nastouli
Katie Johnson
Sharon Glaysher
Scott Elliott
Helen Umpleby
Emanuela Pelosi
Emma Thomson
Cristina Venturini
Anna Riddell
Alison Cox
Andrew C Hayward
Malin Bergström
David Harrington
Charlotte Williams
Tanzina Haque
Dianne Irish
Adrienn Angyal
Marios Margaritis
Moira Spyer
Florencia Boshier
José Afonso Guerra-Assunção
Adela Alcolea-Medina
Angela Beckett
Themoula Charalampous
Raghavendran Kulasegaran Shylini
Beatrix Kele
Irene Monahan
Guy Mollett
Matthew Parker
Sunando Roy
Joshua Taylor
Sophie Weller
Eleri Wilson-Davies
Phillip Wade
Joseph Hughes
Tabitha Mahungu
Cassie Pope
Samuel Robson
Kordo Saeed
Thushan de Silva
Luke Snell
Adam A Witney
James Blackstone
Leanne Hockey
Georgia Marley
Christine Peters
Flavia Flaviani
Bindi Patel
Tom G S Williams
Rahul Batra
Jonathan D Edgeworth
Pinglawathee Madona
Jennifer Hart
Juanita Pang
Helena Tutill
Nadua Bayzid
Marius Cotic
Luke Green
Benjamin Lindsey
Amy State
Alison Cope
Peijun Zhang
Max Whiteley
Marta Gallis Ramalho
Stella Christou
Stavroula Louka
Hailey Hornsby
Benjamin Foulkes
Paige Wolverson
Joe Heffer
Nikki Smith
Salman Goudarzi
Chris Fearn
Kate Cook
Katie Loveson
Adhyana Mahamana
Buddhini Samaraweera
Siona Silveira
Stephen Aplin
Sarah Jeremiah
Matthew Harvey
Thea Sass
Ngee Keong Tan
Claudia Cardoso Pereira
Dan Frampton
Matt Byott
Judith Heaney
Emilie Sanchez
Stavroula M Paraskevopoulou
Source :
BMJ Open Respiratory Research, Vol 8, Iss 1 (2021)
Publication Year :
2021
Publisher :
BMJ Publishing Group, 2021.

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.

Details

Language :
English
ISSN :
20524439
Volume :
8
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMJ Open Respiratory Research
Publication Type :
Academic Journal
Accession number :
edsdoj.8a895e04928046eab408c7338ade581c
Document Type :
article
Full Text :
https://doi.org/10.1136/bmjresp-2021-001029