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Applying mixture model methods to SARS-CoV-2 serosurvey data from Geneva.
Bouman, Judith A; Kadelka, Sarah; Stringhini, Silvia; Pennacchio, Francesco; Meyer, Benjamin; Yerly, Sabine; Kaiser, Laurent; Guessous, Idris; Azman, Andrew S; Bonhoeffer, Sebastian; Regoes, Roland R.
  • Bouman JA; Institute of Integrative Biology, ETH Zurich, Zurich, Switzerland. Electronic address: judith.bouman@env.ethz.ch.
  • Kadelka S; Institute of Integrative Biology, ETH Zurich, Zurich, Switzerland.
  • Stringhini S; Division of Primary Care, Geneva University Hospitals, Geneva, Switzerland; Department of Health and Community Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland; University Centre for General Medicine and Public Health, University of Lausanne, Lausanne, Switzerland.
  • Pennacchio F; Division of Primary Care, Geneva University Hospitals, Geneva, Switzerland.
  • Meyer B; Centre for Vaccinology, Department of Pathology and Immunology, University of Geneva, Geneva, Switzerland.
  • Yerly S; Division of Laboratory Medicine, Geneva University Hospitals, Geneva, Switzerland; Geneva Center for Emerging Viral Diseases and Laboratory of Virology, Geneva University Hospitals, Geneva, Switzerland.
  • Kaiser L; Geneva Center for Emerging Viral Diseases and Laboratory of Virology, Geneva University Hospitals, Geneva, Switzerland; Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland; Department of Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Guessous I; Division of Primary Care, Geneva University Hospitals, Geneva, Switzerland; Department of Health and Community Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Azman AS; Department of Health and Community Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland; Institute of Global Health, Faculty of Medicine, University of Geneva, Geneva, Switzerland; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Bonhoeffer S; Institute of Integrative Biology, ETH Zurich, Zurich, Switzerland.
  • Regoes RR; Institute of Integrative Biology, ETH Zurich, Zurich, Switzerland. Electronic address: roland.regoes@env.ethz.ch.
Epidemics ; 39: 100572, 2022 06.
Article in English | MEDLINE | ID: covidwho-1821233
ABSTRACT
Serosurveys are an important tool to estimate the true extent of the current SARS-CoV-2 pandemic. So far, most serosurvey data have been analyzed with cutoff-based methods, which dichotomize individual measurements into sero-positives or negatives based on a predefined cutoff. However, mixture model methods can gain additional information from the same serosurvey data. Such methods refrain from dichotomizing individual values and instead use the full distribution of the serological measurements from pre-pandemic and COVID-19 controls to estimate the cumulative incidence. This study presents an application of mixture model methods to SARS-CoV-2 serosurvey data from the SEROCoV-POP study from April and May 2020 in Geneva (2766 individuals). Besides estimating the total cumulative incidence in these data (8.1% (95% CI 6.8%-9.9%)), we applied extended mixture model methods to estimate an indirect indicator of disease severity, which is the fraction of cases with a distribution of antibody levels similar to hospitalized COVID-19 patients. This fraction is 51.2% (95% CI 15.2%-79.5%) across the full serosurvey, but differs between three age classes 21.4% (95% CI 0%-59.6%) for individuals between 5 and 40 years old, 60.2% (95% CI 21.5%-100%) for individuals between 41 and 65 years old and 100% (95% CI 20.1%-100%) for individuals between 66 and 90 years old. Additionally, we find a mismatch between the inferred negative distribution of the serosurvey and the validation data of pre-pandemic controls. Overall, this study illustrates that mixture model methods can provide additional insights from serosurvey data.
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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 Limits: Adult / Humans / Young adult Language: English Journal: Epidemics Year: 2022 Document Type: Article

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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 Limits: Adult / Humans / Young adult Language: English Journal: Epidemics Year: 2022 Document Type: Article