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Association of SARS-CoV-2 viral load distributions with individual demographics and suspected variant type: results from the Liverpool community testing pilot, England, 6 November 2020 to 8 September 2021.
Hughes, David M; Cheyne, Christopher P; Ashton, Matthew; Coffey, Emer; Crozier, Alex; Semple, Malcolm G; Buchan, Iain; García-Fiñana, Marta.
  • Hughes DM; Department of Health Data Science, Institute of Population Health, University of Liverpool, Liverpool, United Kingdom.
  • Cheyne CP; Department of Health Data Science, Institute of Population Health, University of Liverpool, Liverpool, United Kingdom.
  • Ashton M; Department of Public Health, Liverpool City Council, Liverpool, United Kingdom.
  • Coffey E; Department of Public Health, Liverpool City Council, Liverpool, United Kingdom.
  • Crozier A; Division of biosciences, University College London, London, United Kingdom.
  • Semple MG; Health Protection Research Unity in Emerging and Zoonotic Infections, Institute of Infection, Veterinary and Ecological Science, University of Liverpool, United Kingdom.
  • Buchan I; Department of Public Health, Policy and Systems, Institute of Population Health, University of Liverpool, Liverpool, United Kingdom.
  • García-Fiñana M; Department of Health Data Science, Institute of Population Health, University of Liverpool, Liverpool, United Kingdom.
Euro Surveill ; 28(4)2023 01.
Article in English | MEDLINE | ID: covidwho-2215129
ABSTRACT
BackgroundThe PCR quantification cycle (Cq) is a proxy measure of the viral load of a SARS-CoV-2-infected individual.AimTo investigate if Cq values vary according to different population characteristics, in particular demographic ones, and within the COVID-19 pandemic context, notably the SARS-CoV-2 type/variant individuals get infected with.MethodsWe considered all positive PCR results from Cheshire and Merseyside, England, between 6 November 2020 and 8 September 2021. Cq distributions were inspected with Kernel density estimates. Multivariable quantile regression models assessed associations between people's features and Cq.ResultsWe report Cq values for 188,821 SARS-CoV-2 positive individuals. Median Cqs increased with decreasing age for suspected wild-type virus and Alpha variant infections, but less so, if not, for Delta. For example, compared to 30-39-year-olds (median age group), 5-11-year-olds exhibited 1.8 (95% CI 1.5 to 2.1), 2.2 (95% CI 1.8 to 2.6) and 0.8 (95% CI 0.6 to 0.9) higher median Cqs for suspected wild-type, Alpha and Delta positives, respectively, in multivariable analysis. 12-18-year-olds also had higher Cqs for wild-type and Alpha positives, however, not for Delta. Overall, in univariable analysis, suspected Delta positives reported 2.8 lower median Cqs than wild-type positives (95% CI 2.7 to 2.8; p < 0.001). Suspected Alpha positives had 1.5 (95% CI 1.4 to 1.5; p < 0.001) lower median Cqs than wild type.ConclusionsWild-type- or Alpha-infected school-aged children (5-11-year-olds) might transmit less than adults (> 18 years old), but have greater mixing exposures. Smaller differences in viral loads with age occurred in suspected Delta infections. Suspected-Alpha- or Delta-infections involved higher viral loads than wild type, suggesting increased transmission risk. COVID-19 control strategies should consider age and dominant variant.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Variants Limits: Adolescent / Adult / Child / Humans Country/Region as subject: Europa Language: English Journal subject: Communicable Diseases Year: 2023 Document Type: Article Affiliation country: 1560-7917.ES.2023.28.4.2200129

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Variants Limits: Adolescent / Adult / Child / Humans Country/Region as subject: Europa Language: English Journal subject: Communicable Diseases Year: 2023 Document Type: Article Affiliation country: 1560-7917.ES.2023.28.4.2200129