Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7
Increased mortality in community-tested cases of SARS-CoV-2 lineage B.1.1.7
复制标题
DOI:
10.1101/2021.02.01.21250959
复制
发表时间:
2021-03-15
期刊:
影响因子:
64.8
通讯作者:
Keogh, Ruth H.
中科院分区:
文献类型:
--
作者:
Davies, Nicholas G.;Jarvis, Christopher I.;Keogh, Ruth H.
SARS-CoV-2 lineage B.1.1.7, a variant that was first detected in the UK in September 2020(1), has spread to multiple countries worldwide. Several studies have established that B.1.1.7 is more transmissible than pre-existing variants, but have not identified whether it leads to any change in disease severity. Here we analyse a dataset that links 2,245,263 positive SARS-CoV-2 community tests and 17,452 deaths associated with COVID-19 in England from 1 November 2020 to 14 February 2021. For 1,146,534 (51%) ofthese tests, the presence or absence of B.1.1.7 can be identified because mutations in this lineage prevent PCR amplification ofthe spike (S) gene target (known as Sgene target failure (SGTF)(1)). On the basis of 4,945 deaths with known SGTF status, we estimate that the hazard of death associated with SGTF is 55% (95% confidence interval, 39-72%) higher than in cases without SGTF after adjustment for age, sex, ethnicity, deprivation, residence in a care home, the local authority of residence and test date. This corresponds to the absolute risk of death for a 55-69-year-old man increasing from 0.6% to 0.9% (95% confidence interval, 0.8-1.0%) within 28 days of a positive test in the community. Correcting for misclassification of SGTF and missingness in SGTF status, we estimate that the hazard of death associated with B.1.1.7 is 61% (42-82%) higher than with pre-existing variants. Our analysis suggests that B.1.1.7 is not only more transmissible than pre-existing SARS-CoV-2 variants, but may also cause more severe illness.