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Seroprevalence and infection fatality rate of the SARS-CoV-2 Omicron variant in Denmark: A nationwide serosurveillance study.
Erikstrup, Christian; Laksafoss, Anna Damkjær; Gladov, Josephine; Kaspersen, Kathrine Agergård; Mikkelsen, Susan; Hindhede, Lotte; Boldsen, Jens Kjærgaard; Jørgensen, Signe Winther; Ethelberg, Steen; Holm, Dorte Kinggaard; Bruun, Mie Topholm; Nissen, Janna; Schwinn, Michael; Brodersen, Thorsten; Mikkelsen, Christina; Sækmose, Susanne Gjørup; Sørensen, Erik; Harritshøj, Lene Holm; Aagaard, Bitten; Dinh, Khoa Manh; Busch, Michael P; Jørgensen, Charlotte Sværke; Krause, Tyra Grove; Ullum, Henrik; Ostrowski, Sisse Rye; Espenhain, Laura; Pedersen, Ole Birger Vesterager.
  • Erikstrup C; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Laksafoss AD; Danish Big Data Centre for Environment and Health (BERTHA), Aarhus University, DK-8000 Aarhus C, Denmark.
  • Gladov J; Department of Clinical Medicine, Aarhus University, DK-8000 Aarhus C, Denmark.
  • Kaspersen KA; Epidemiological Infectious Disease Preparedness, Statens Serum Institut, DK-2300 Copenhagen S, Denmark.
  • Mikkelsen S; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Hindhede L; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Boldsen JK; Danish Big Data Centre for Environment and Health (BERTHA), Aarhus University, DK-8000 Aarhus C, Denmark.
  • Jørgensen SW; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Ethelberg S; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Holm DK; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Bruun MT; Danish Big Data Centre for Environment and Health (BERTHA), Aarhus University, DK-8000 Aarhus C, Denmark.
  • Nissen J; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Schwinn M; Epidemiological Infectious Disease Preparedness, Statens Serum Institut, DK-2300 Copenhagen S, Denmark.
  • Brodersen T; Department of Clinical Immunology, Odense University Hospital, DK-5000 Odense, Denmark.
  • Mikkelsen C; Department of Clinical Immunology, Odense University Hospital, DK-5000 Odense, Denmark.
  • Sækmose SG; Department of Clinical Immunology, Copenhagen University Hospital, DK-2100 Copenhagen Ø, Denmark.
  • Sørensen E; Department of Clinical Immunology, Copenhagen University Hospital, DK-2100 Copenhagen Ø, Denmark.
  • Harritshøj LH; Department of Clinical Immunology, Zealand University Hospital, DK-4700 Naestved, Denmark.
  • Aagaard B; Department of Clinical Immunology, Copenhagen University Hospital, DK-2100 Copenhagen Ø, Denmark.
  • Dinh KM; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health, Copenhagen University, DK-2200 Copenhagen Ø, Denmark.
  • Busch MP; Department of Clinical Immunology, Zealand University Hospital, DK-4700 Naestved, Denmark.
  • Jørgensen CS; Department of Clinical Immunology, Copenhagen University Hospital, DK-2100 Copenhagen Ø, Denmark.
  • Krause TG; Department of Clinical Immunology, Copenhagen University Hospital, DK-2100 Copenhagen Ø, Denmark.
  • Ullum H; Department of Clinical Immunology, Aalborg University Hospital, DK-9000 Aalborg, Denmark.
  • Ostrowski SR; Department of Clinical Immunology, Aarhus University Hospital, DK-8200 Aarhus N, Denmark.
  • Espenhain L; Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Pedersen OBV; Vitalant Research Institute, San Francisco, CA, USA.
Lancet Reg Health Eur ; 21: 100479, 2022 Oct.
Article in English | MEDLINE | ID: covidwho-1977613
ABSTRACT

Background:

Introduction of the Omicron variant caused a steep rise in SARS-CoV-2 infections despite high vaccination coverage in the Danish population. We used blood donor serosurveillance to estimate the percentage of recently infected residents in the similarly aged background population with no known comorbidity.

Methods:

To detect SARS-CoV-2 antibodies induced due to recent infection, and not vaccination, we assessed anti-nucleocapsid (anti-N) immunoglobulin G (IgG) in blood donor samples. Individual level data on SARS-CoV-2 RT-PCR results and vaccination status were available. Anti-N IgG was measured fortnightly from January 18 to April 3, 2022. Samples from November 2021 were analysed to assess seroprevalence before introduction of the Omicron variant in Denmark.

Findings:

A total of 43 088 donations from 35 309 Danish blood donors aged 17-72 years were screened. In November 2021, 1·2% (103/8 701) of donors had detectable anti-N IgG antibodies. Adjusting for test sensitivity (estimates ranging from 74%-81%) and November seroprevalence, we estimate that 66% (95% confidence intervals (CI) 63%-70%) of the healthy, similarly aged Danish population had been infected between November 1, 2021, and March 15, 2022. One third of infections were not captured by SARS-CoV-2 RT-PCR testing. The infection fatality rate (IFR) was 6·2 (CI 5·1-7·5) per 100 000 infections.

Interpretation:

Screening for anti-N IgG and linkage to national registers allowed us to detect recent infections and accurately assess assay sensitivity in vaccinated or previously infected individuals during the Omicron outbreak. The IFR was lower than during previous waves.

Funding:

The Danish Ministry of Health.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Observational study Topics: Vaccines / Variants Language: English Journal: Lancet Reg Health Eur Year: 2022 Document Type: Article Affiliation country: J.LANEPE.2022.100479

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Observational study Topics: Vaccines / Variants Language: English Journal: Lancet Reg Health Eur Year: 2022 Document Type: Article Affiliation country: J.LANEPE.2022.100479