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Global SARS-CoV-2 seroprevalence from January 2020 to April 2022: A systematic review and meta-analysis of standardized population-based studies.
Bergeri, Isabel; Whelan, Mairead G; Ware, Harriet; Subissi, Lorenzo; Nardone, Anthony; Lewis, Hannah C; Li, Zihan; Ma, Xiaomeng; Valenciano, Marta; Cheng, Brianna; Al Ariqi, Lubna; Rashidian, Arash; Okeibunor, Joseph; Azim, Tasnim; Wijesinghe, Pushpa; Le, Linh-Vi; Vaughan, Aisling; Pebody, Richard; Vicari, Andrea; Yan, Tingting; Yanes-Lane, Mercedes; Cao, Christian; Clifton, David A; Cheng, Matthew P; Papenburg, Jesse; Buckeridge, David; Bobrovitz, Niklas; Arora, Rahul K; Van Kerkhove, Maria D.
  • Bergeri I; World Health Organization, Geneva, Switzerland.
  • Whelan MG; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Ware H; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Subissi L; World Health Organization, Geneva, Switzerland.
  • Nardone A; World Health Organization, Geneva, Switzerland.
  • Lewis HC; Epiconcept, Paris, France.
  • Li Z; World Health Organization, Geneva, Switzerland.
  • Ma X; World Health Organization, Regional Office for Africa, Brazzaville, Congo.
  • Valenciano M; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Cheng B; Faculty of Engineering, University of Waterloo, Waterloo, Ontario, Canada.
  • Al Ariqi L; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Rashidian A; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
  • Okeibunor J; World Health Organization, Geneva, Switzerland.
  • Azim T; Epiconcept, Paris, France.
  • Wijesinghe P; World Health Organization, Geneva, Switzerland.
  • Le LV; School of Population and Global Health, McGill University, Montreal, Quebec, Canada.
  • Vaughan A; World Health Organization, Regional Office for the Eastern Mediterranean, Cairo, Egypt.
  • Pebody R; World Health Organization, Regional Office for South-East Asia, New Delhi, India.
  • Vicari A; World Health Organization, Regional Office for Africa, Brazzaville, Congo.
  • Yan T; World Health Organization, Regional Office for South-East Asia, New Delhi, India.
  • Yanes-Lane M; World Health Organization, Regional Office for South-East Asia, New Delhi, India.
  • Cao C; World Health Organization, Regional Office for the Western Pacific, Manila, Philippines.
  • Clifton DA; World Health Organization Regional Office for Europe, Copenhagen, Denmark.
  • Cheng MP; World Health Organization Regional Office for Europe, Copenhagen, Denmark.
  • Papenburg J; World Health Organization, Regional Office for the Americas (Pan American Health Organization), Washington DC, United States of America.
  • Buckeridge D; Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Bobrovitz N; COVID-19 Immunity Task Force Secretariat, McGill University, Montreal, Canada.
  • Arora RK; Centre for Health Informatics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Van Kerkhove MD; Institute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom.
PLoS Med ; 19(11): e1004107, 2022 Nov.
Article in English | MEDLINE | ID: covidwho-2116445
ABSTRACT

BACKGROUND:

Our understanding of the global scale of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection remains incomplete Routine surveillance data underestimate 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 the World Health Organization's Unity protocol (WHO Unity) for general population seroepidemiological studies, to estimate the extent of population infection and seropositivity to the virus 2 years into the pandemic. METHODS AND

FINDINGS:

We conducted a systematic review and meta-analysis, searching MEDLINE, Embase, Web of Science, preprints, and grey literature for SARS-CoV-2 seroprevalence published between January 1, 2020 and May 20, 2022. 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 underascertainment; meta-analyzed differences in seroprevalence between demographic subgroups such as age and sex; and identified national factors associated with seroprevalence using meta-regression. We identified 513 full texts reporting 965 distinct seroprevalence studies (41% low- and middle-income countries [LMICs]) sampling 5,346,069 participants between January 2020 and April 2022, including 459 low/moderate risk of bias studies with national/subnational scope in further analysis. By September 2021, global SARS-CoV-2 seroprevalence from infection or vaccination was 59.2%, 95% CI [56.1% to 62.2%]. Overall seroprevalence rose steeply in 2021 due to infection in some regions (e.g., 26.6% [24.6 to 28.8] to 86.7% [84.6% to 88.5%] in Africa in December 2021) and vaccination and infection in others (e.g., 9.6% [8.3% to 11.0%] in June 2020 to 95.9% [92.6% to 97.8%] in December 2021, in European high-income countries [HICs]). After the emergence of Omicron in March 2022, infection-induced seroprevalence rose to 47.9% [41.0% to 54.9%] in Europe HIC and 33.7% [31.6% to 36.0%] in Americas HIC. 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 to 9 years and adults 60+ were at lower risk of seropositivity than adults 20 to 29 (p < 0.001 and p = 0.005, respectively). In a multivariable model using prevaccination data, stringent public health and social measures were associated with lower seroprevalence (p = 0.02). The main limitations of our methodology include that some estimates were driven by certain countries or populations being overrepresented.

CONCLUSIONS:

In this study, we observed that global seroprevalence has risen considerably over time and with regional variation; however, over one-third of the global population are seronegative to the SARS-CoV-2 virus. Our estimates of infections based on seroprevalence far exceed reported Coronavirus Disease 2019 (COVID-19) cases. Quality and standardized seroprevalence studies are essential to inform COVID-19 response, particularly in resource-limited regions.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Topics: Vaccines / Variants Limits: Adult / Child / Humans Language: English Journal: PLoS Med Journal subject: Medicine Year: 2022 Document Type: Article Affiliation country: Journal.pmed.1004107

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Topics: Vaccines / Variants Limits: Adult / Child / Humans Language: English Journal: PLoS Med Journal subject: Medicine Year: 2022 Document Type: Article Affiliation country: Journal.pmed.1004107