Silvia Stringhini1, María-Eugenia Zaballa2, Javier Perez-Saez3, Nick Pullen2, Carlos de Mestral2, Attilio Picazio2, Francesco Pennacchio2, Ania Wisniak2, Aude Richard4, Helene Baysson4, Andrea Loizeau4, Jean-François Balavoine5, Didier Trono6, Didier Pittet7, Klara Posfay-Barbe8, Antoine Flahault5, François Chappuis9, Omar Kherad10, Nicolas Vuilleumier11, Laurent Kaiser12, Andrew S Azman13, Idris Guessous4. 1. Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. Electronic address: silvia.stringhini@hcuge.ch. 2. Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland. 3. Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA. 4. Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. 5. Faculty of Medicine, University of Geneva, Switzerland. 6. School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland. 7. Infection Control Program and WHO Collaborating Centre on Patient Safety, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. 8. Division of General Pediatrics, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. 9. Division of Tropical and Humanitarian Medicine, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. 10. Faculty of Medicine, University of Geneva, Switzerland; Division of Internal Medicine, Hôpital de la Tour, Geneva, Switzerland. 11. Division of Laboratory Medicine, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. 12. Geneva Center for Emerging Viral Diseases, Geneva University Hospitals, Geneva, Switzerland; Faculty of Medicine, University of Geneva, Switzerland. 13. Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
After the first pandemic wave in Europe, seroprevalence surveys revealed that roughly one in ten individuals had been infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Our Geneva-based seroprevalence study revealed that infections were less common in young children (<9 years) than in older children and adults, but at the time of the study individuals were confined and schools were closed. Since autumn, 2020, Europe has experienced a rapid increase in reported infections, with SARS-CoV-2 incidence in some countries largely surpassing that of the first wave. Due to changes in test availability, policy, and care-seeking behaviours, it is unclear how to compare current case reports with the first wave and how these relate to undetected infection rates.To estimate SARS-CoV-2 seroprevalence in the general population and determine whether age disparities have persisted through the second wave, we repeated a representative serosurvey of the Geneva population using a stratified random sample (based on age, sex, and education level) of individuals aged 18–64 years from our previous study and an independent random sample of individuals aged 0–18 years and 65 years and older who were identified from resident registers of the Swiss Federal Office of Statistics. We tested participants for anti-SARS-CoV-2 total immunoglobulins targeting the spike protein (Elecsys anti-SARS-CoV-2 S; Roche Diagnostics, Rotkreuz, Switzerland) following manufacturer's recommendations (≥0·8 U/mL considered seropositive). We used a previously published Bayesian model accounting for household clustering, test performance, and age distribution in the Geneva population.Between Nov 23, and Dec 23, 2020, we recruited 4000 participants aged 0–96 years (53·4% women; 25·4% <18 years), of whom 820 were seropositive, yielding a seroprevalence of 21·1% (95% credible interval [CrI] 19·2–23·1). We found similar seroprevalence among men and women, but large differences across age groups (appendix p 2). Compared with adults aged 25–34 years, children aged 6 years and older and adolescents had similar seroprevalence, whereas children aged 0–5 years were 43% less likely to be seropositive, and adults aged 65–74 years and those aged 75 years and older were 42% and 64% less likely to be seropositive, respectively (appendix p 2). We estimated that each virologically confirmed SARS-CoV-2 infection represented 2·7 infections (95% CrI 2·3–3·1; appendix pp 3–5) in the community, substantially lower than in the first wave (11·6), probably due to changed testing practices.Despite seroprevalence doubling in Geneva since the end of the first wave, most of the population remains unexposed, including more than 90% of adults aged 75 years and older, who have very high mortality risk.3, 4 Although children aged 6 years and older have a similar infection risk as adults, younger children have a lower infection risk. These results should inform policy-makers worldwide, reinforcing the need for continuous measures to contain SARS-CoV-2 spread, despite growing pandemic fatigue in the population, and to avoid potentially catastrophic COVID-19-related hospitalisations and deaths in the critical months ahead.
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