Household transmission of COVID-19 cases associated with SARS-CoV-2 delta variant (B.1.617.2): national case-control study.

COVID-19 Delta,household England SARS-CoV-2 transmission variant

Journal

The Lancet regional health. Europe
ISSN: 2666-7762
Titre abrégé: Lancet Reg Health Eur
Pays: England
ID NLM: 101777707

Informations de publication

Date de publication:
Jan 2022
Historique:
pubmed: 4 11 2021
medline: 4 11 2021
entrez: 3 11 2021
Statut: ppublish

Résumé

The SARS-CoV-2 Delta variant (B.1.617.2), first detected in India, has rapidly become the dominant variant in England. Early reports suggest this variant has an increased growth rate suggesting increased transmissibility. This study indirectly assessed differences in transmissibility between the emergent Delta variant compared to the previously dominant Alpha variant (B.1.1.7). A matched case-control study was conducted to estimate the odds of household transmission (≥ 2 cases within 14 days) for Delta variant index cases compared with Alpha cases. Cases were derived from national surveillance data (March to June 2021). One-to-two matching was undertaken on geographical location of residence, time period of testing and property type, and a multivariable conditional logistic regression model was used for analysis. In total 5,976 genomically sequenced index cases in household clusters were matched to 11,952 sporadic index cases (single case within a household). 43.3% (n=2,586) of cases in household clusters were confirmed Delta variant compared to 40.4% (n= 4,824) of sporadic cases. The odds ratio of household transmission was 1.70 among Delta variant cases (95% CI 1.48-1.95, p <0.001) compared to Alpha cases after adjusting for age, sex, ethnicity, index of multiple deprivation (IMD), number of household contacts and vaccination status of index case. We found evidence of increased household transmission of SARS-CoV-2 Delta variant, potentially explaining its success at displacing Alpha variant as the dominant strain in England. With the Delta variant now having been detected in many countries worldwide, the understanding of the transmissibility of this variant is important for informing infection prevention and control policies internationally.

Sections du résumé

BACKGROUND BACKGROUND
The SARS-CoV-2 Delta variant (B.1.617.2), first detected in India, has rapidly become the dominant variant in England. Early reports suggest this variant has an increased growth rate suggesting increased transmissibility. This study indirectly assessed differences in transmissibility between the emergent Delta variant compared to the previously dominant Alpha variant (B.1.1.7).
METHODS METHODS
A matched case-control study was conducted to estimate the odds of household transmission (≥ 2 cases within 14 days) for Delta variant index cases compared with Alpha cases. Cases were derived from national surveillance data (March to June 2021). One-to-two matching was undertaken on geographical location of residence, time period of testing and property type, and a multivariable conditional logistic regression model was used for analysis.
FINDINGS RESULTS
In total 5,976 genomically sequenced index cases in household clusters were matched to 11,952 sporadic index cases (single case within a household). 43.3% (n=2,586) of cases in household clusters were confirmed Delta variant compared to 40.4% (n= 4,824) of sporadic cases. The odds ratio of household transmission was 1.70 among Delta variant cases (95% CI 1.48-1.95, p <0.001) compared to Alpha cases after adjusting for age, sex, ethnicity, index of multiple deprivation (IMD), number of household contacts and vaccination status of index case.
INTERPRETATION CONCLUSIONS
We found evidence of increased household transmission of SARS-CoV-2 Delta variant, potentially explaining its success at displacing Alpha variant as the dominant strain in England. With the Delta variant now having been detected in many countries worldwide, the understanding of the transmissibility of this variant is important for informing infection prevention and control policies internationally.

Identifiants

pubmed: 34729548
doi: 10.1016/j.lanepe.2021.100252
pii: S2666-7762(21)00238-6
pmc: PMC8552812
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100252

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19027
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T030062/1
Pays : United Kingdom

Informations de copyright

Crown Copyright © 2021 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

GD's employer, Public Health England, has received funding from GlaxoSmithKline for a research project related to seasonal influenza and antiviral treatment; this project preceded and had no relation to COVID-19, and GD had no role in and received no funding from the project. All other authors declare no competing interests.

Références

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Auteurs

Hester Allen (H)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Amoolya Vusirikala (A)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Joe Flannagan (J)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Katherine A Twohig (KA)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Asad Zaidi (A)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Dimple Chudasama (D)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Theresa Lamagni (T)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Natalie Groves (N)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Charlie Turner (C)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Christopher Rawlinson (C)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Jamie Lopez-Bernal (J)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Ross Harris (R)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Andre Charlett (A)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Gavin Dabrera (G)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Meaghan Kall (M)

National Infection Service, Public Health England, Colindale, London, NW9 5EQ, UK.

Classifications MeSH