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COVID-19 due to the B.1.617.2 (Delta) variant compared to B.1.1.7 (Alpha) variant of SARS-CoV-2: a prospective observational cohort study.
Kläser, Kerstin; Molteni, Erika; Graham, Mark; Canas, Liane S; Österdahl, Marc F; Antonelli, Michela; Chen, Liyuan; Deng, Jie; Murray, Benjamin; Kerfoot, Eric; Wolf, Jonathan; May, Anna; Fox, Ben; Capdevila, Joan; Modat, Marc; Hammers, Alexander; Spector, Tim D; Steves, Claire J; Sudre, Carole H; Ourselin, Sebastien; Duncan, Emma L.
  • Kläser K; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Molteni E; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Graham M; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Canas LS; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Österdahl MF; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, St Thomas' Hospital Campus, 3rd Floor South Wing Block D, Westminster Bridge Road, London, SE1 7EH, UK.
  • Antonelli M; Department of Aging and Health, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Chen L; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Deng J; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Murray B; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Kerfoot E; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Wolf J; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • May A; ZOE Limited, London, UK.
  • Fox B; ZOE Limited, London, UK.
  • Capdevila J; ZOE Limited, London, UK.
  • Hammers A; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Spector TD; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Steves CJ; King's College London & Guy's and St Thomas' PET Centre, London, UK.
  • Sudre CH; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, St Thomas' Hospital Campus, 3rd Floor South Wing Block D, Westminster Bridge Road, London, SE1 7EH, UK.
  • Ourselin S; Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, St Thomas' Hospital Campus, 3rd Floor South Wing Block D, Westminster Bridge Road, London, SE1 7EH, UK.
  • Duncan EL; Department of Aging and Health, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Sci Rep ; 12(1): 10904, 2022 06 28.
Article in English | MEDLINE | ID: covidwho-1908282
ABSTRACT
The Delta (B.1.617.2) variant was the predominant UK circulating SARS-CoV-2 strain between May and December 2021. How Delta infection compares with previous variants is unknown. This prospective observational cohort study assessed symptomatic adults participating in the app-based COVID Symptom Study who tested positive for SARS-CoV-2 from May 26 to July 1, 2021 (Delta overwhelmingly the predominant circulating UK variant), compared (11, age- and sex-matched) with individuals presenting from December 28, 2020 to May 6, 2021 (Alpha (B.1.1.7) the predominant variant). We assessed illness (symptoms, duration, presentation to hospital) during Alpha- and Delta-predominant timeframes; and transmission, reinfection, and vaccine effectiveness during the Delta-predominant period. 3581 individuals (aged 18 to 100 years) from each timeframe were assessed. The seven most frequent symptoms were common to both variants. Within the first 28 days of illness, some symptoms were more common with Delta versus Alpha infection (including fever, sore throat, and headache) and some vice versa (dyspnoea). Symptom burden in the first week was higher with Delta versus Alpha infection; however, the odds of any given symptom lasting ≥ 7 days was either lower or unchanged. Illness duration ≥ 28 days was lower with Delta versus Alpha infection, though unchanged in unvaccinated individuals. Hospitalisation for COVID-19 was unchanged. The Delta variant appeared more (1.49) transmissible than Alpha. Re-infections were low in all UK regions. Vaccination markedly reduced the risk of Delta infection (by 69-84%). We conclude that COVID-19 from Delta or Alpha infections is similar. The Delta variant is more transmissible than Alpha; however, current vaccines showed good efficacy against disease. This research framework can be useful for future comparisons with new emerging variants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Hepatitis D / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Humans Language: English Journal: Sci Rep Year: 2022 Document Type: Article Affiliation country: S41598-022-14016-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Hepatitis D / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Humans Language: English Journal: Sci Rep Year: 2022 Document Type: Article Affiliation country: S41598-022-14016-0