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Global epidemiology of SARS-CoV-2 infection: a systematic review and meta-analysis of standardized population-based seroprevalence studies, Jan 2020-Oct 2021
Isabel Bergeri; Mairead Whelan; Harriet Ware; Lorenzo Subissi; Anthony Nardone; Hannah C Lewis; Zihan Li; Xiaomeng Ma; Marta Valenciano; Brianna Cheng; Lubna Al Ariqi; Arash Rashidian; Joseph Okeibunor; Tasnim Azim; Pushpa Wijesinghe; Linh-Vi Le; Aisling Vaughan; Richard Pebody; Andrea Vicari; Tingting Yan; Mercedes Yanes-Lane; Christian Cao; David A. Clifton; Matthew P Cheng; Jesse Papenburg; David Buckeridge; Niklas Bobrovitz; Rahul K Arora; Maria D. Van Kerkhove; - Unity Studies Collaborator Group.
Afiliación
  • Isabel Bergeri; World Health Organization, Geneva, Switzerland
  • Mairead Whelan; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada
  • Harriet Ware; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada
  • Lorenzo Subissi; World Health Organization, Geneva, Switzerland
  • Anthony Nardone; Epiconcept, Paris, France; World Health Organization, Geneva, Switzerland
  • Hannah C Lewis; World Health Organization, Geneva, Switzerland; World Health Organization, Regional Office for Africa, Brazzaville, Congo
  • Zihan Li; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada; University of Waterloo, Canada
  • Xiaomeng Ma; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Canada; University of Toronto, Canada
  • Marta Valenciano; Epiconcept, Paris, France; World Health Organization, Geneva, Switzerland
  • Brianna Cheng; World Health Organization, Geneva, Switzerland
  • Lubna Al Ariqi; World Health Organization, Regional Office for the Eastern Mediterranean, Cairo, Egypt
  • Arash Rashidian; World Health Organization, Regional Office for the Eastern Mediterranean, Cairo, Egypt
  • Joseph Okeibunor; World Health Organization, Regional Office for Africa, Brazzaville, Congo
  • Tasnim Azim; World Health Organization, Regional Office for South-East Asia, New Delhi, India
  • Pushpa Wijesinghe; World Health Organization, Regional Office for South-East Asia, New Delhi, India
  • Linh-Vi Le; World Health Organization, Regional Office for the Western Pacific, Manila, Philippines
  • Aisling Vaughan; World Health Organization Regional Office for Europe, Copenhagen, Denmark
  • Richard Pebody; World Health Organization Regional Office for Europe, Copenhagen, Denmark
  • Andrea Vicari; World Health Organization, Regional Office for the Americas (Pan American Health Organization), Washington DC, United States of
  • Tingting Yan; University of Toronto, Canada
  • Mercedes Yanes-Lane; McGill University, Montreal, Canada
  • Christian Cao; University of Calgary, Canada
  • David A. Clifton; Institute of Biomedical Engineering, University of Oxford, UK
  • Matthew P Cheng; McGill University Health Centre, Montreal, Quebec, Canada
  • Jesse Papenburg; McGill University Health Centre, Montreal, Quebec, Canada
  • David Buckeridge; McGill University, Montreal, Canada;
  • Niklas Bobrovitz; University of Toronto, University of Calgary, Canada
  • Rahul K Arora; University of Calgary, Canada; University of Oxford, UK
  • Maria D. Van Kerkhove; World Health Organization, Geneva, Switzerland
  • - Unity Studies Collaborator Group;
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21267791
ABSTRACT
BackgroundOur understanding of the global scale of SARS-CoV-2 infection remains incomplete routine surveillance data underestimates infection and cannot infer on population immunity, there is a predominance of asymptomatic infections, and uneven access to diagnostics. We meta-analyzed SARS-CoV-2 seroprevalence studies, standardized to those described in WHOs Unity protocol for general population seroepidemiological studies, two years into the pandemic, to estimate the extent of population infection and remaining susceptibility. Methods and FindingsWe conducted a systematic review and meta-analysis, searching MEDLINE, Embase, Web of Science, preprints, and grey literature for SARS-CoV-2 seroprevalence published between 2020-01-01 and 2022-05-20. The review protocol is registered with PROSPERO, (CRD42020183634). We included general population cross-sectional and cohort studies meeting an assay quality threshold (90% sensitivity, 97% specificity; exceptions for humanitarian settings). We excluded studies with an unclear or closed population sample frame. Eligible studies - those aligned with the WHO Unity protocol - were extracted and critically appraised in duplicate, with Risk of Bias evaluated using a modified Joanna Briggs Institute checklist. We meta-analyzed seroprevalence by country and month, pooling to estimate regional and global seroprevalence over time; compared seroprevalence from infection to confirmed cases to estimate under-ascertainment; meta-analyzed differences in seroprevalence between demographic subgroups such as age and sex; and identified national factors associated with seroprevalence using meta-regression. The main limitations of our methodology include that some estimates were driven by certain countries or populations being over-represented. We identified 513 full texts reporting 965 distinct seroprevalence studies (41% LMIC) sampling 5,346,069 participants between January 2020 and April 2022, including 459 low/moderate risk of bias studies with national/sub-national scope in further analysis. By September 2021, global SARS-CoV-2 seroprevalence from infection or vaccination was 59.2%, 95% CI [56.1-62.2%]. Overall seroprevalence rose steeply in 2021 due to infection in some regions (e.g., 26.6% [24.6-28.8] to 86.7% [84.6-88.5%] in Africa in December 2021) and vaccination and infection in others (e.g., 9.6% [8.3-11.0%] to 95.9% [92.6-97.8%] in Europe high-income countries in December 2021). After the emergence of Omicron, infection-induced seroprevalence rose to 47.9% [41.0-54.9%] in EUR HIC and 33.7% [31.6-36.0%] in AMR HIC in March 2022. In 2021 Quarter Three (July to September), median seroprevalence to cumulative incidence ratios ranged from around 21 in the Americas and Europe HICs to over 1001 in Africa (LMICs). Children 0-9 years and adults 60+ were at lower risk of seropositivity than adults 20-29 (p<0.0001 and p=0.005, respectively). In a multivariable model using pre-vaccination data, stringent public health and social measures were associated with lower seroprevalence (p=0.02). ConclusionsIn this study, we observed that global seroprevalence has risen considerably over time and with regional variation, however around 40 % of the global population remains susceptible to SARS-CoV-2 infection. Our estimates of infections based on seroprevalence far exceed reported COVID-19 cases. Quality and standardized seroprevalence studies are essential to inform COVID-19 response, particularly in resource-limited regions.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Experimental_studies / Observational_studies / Prognostic_studies / Rct / Review / Systematic_reviews Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Experimental_studies / Observational_studies / Prognostic_studies / Rct / Review / Systematic_reviews Idioma: En Año: 2021 Tipo del documento: Preprint
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