Evidence map›Paper›PMID 34393019›Full record

ArticleVaccine2021

Prevalence of SARS-CoV-2 IgG antibodies and their association with clinical symptoms of COVID-19 in Estonia (KoroSero-EST-1 study).

Piia Jõgi, Hiie Soeorg, Diana Ingerainen, Mari Soots, Freddy Lättekivi, Paul Naaber, Karolin Toompere, Pärt Peterson, Liis Haljasmägi, Eva Žusinaite and 9 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Autoantibodies Neutralizing Type III Interferons Are Uncommon in Patients with Severe Coronavirus Disease 2019 Pneumonia.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 1 country.

Piia JõgiChildren's Clinic of Tartu University Hospital, N. Lunini 6, 50406 Tartu, Estonia; Department of Pediatrics, Institute of Clinical Medicine, University of Tartu, L. Puusepa 8, 50406 Tartu, Estonia. Electronic address: piia.jogi@kliinikum.ee.
Hiie SoeorgDepartment of Microbiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Diana IngerainenFamily Doctor Center "Järveotsa", Õismäe tee 179, 13517 Tallinn, Estonia.
Mari SootsFamily Doctor Center "Kuressaare", Aia 25a, 93815 Kuressaare, Estonia.
Freddy LättekiviDepartment of Pathophysiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia; Development Centre, United Chancery Service, Tartu University Hospital, Puusepa 8, 50406 Tartu, Estonia.
Paul NaaberDepartment of Microbiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia; SYNLAB Estonia, Tallinn, Estonia.
Karolin ToompereDepartment of Epidemiology and Biostatistics, Institute of Family Medicine and Public Health, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Pärt PetersonMolecular Pathology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Liis HaljasmägiMolecular Pathology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Eva ŽusinaiteInstitute of Technology, Faculty of Science and Technology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.
Hannes VaasChildren's Clinic of Tartu University Hospital, N. Lunini 6, 50406 Tartu, Estonia.
Merit PauskarDepartment of Microbiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Arina ShablinskajaDepartment of Microbiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Katrin KaarnaDevelopment Centre, United Chancery Service, Tartu University Hospital, Puusepa 8, 50406 Tartu, Estonia; Clinical Research Centre, Institute of Clinical Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Heli PalusteMinistry of Social Affairs, Republic of Estonia, Suur-Ameerika 1, 10122 Tallinn, Estonia.
Kai KisandMolecular Pathology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Marje OonaDepartment of Family Medicine, Institute of Family Medicine and Public Health, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
Riina JannoDevelopment Centre, United Chancery Service, Tartu University Hospital, Puusepa 8, 50406 Tartu, Estonia.
Irja LutsarDepartment of Microbiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.
University of Tartu · EETartu University Hospital · EEMinistry of Social Affairs · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn Estonia, during the first wave of COVID-19 total number of cases confirmed by PCR was 13.3/10,000, similar in most regions, including capital Tallinn, but in the hotspot of Estonian epidemic, an island Saaremaa, the cumulative incidence was 166.1/10,000. We aimed to determine the prevalence of SARS-CoV-2 IgG antibodies in these two regions, symptoms associated with infection and factors associated with antibody concentrations.

methodsParticipants were selected using stratified (formed by age decades) random sampling and recruited by general practitioners. IgG or neutralizing antibodies were determined from sera by four assays. Symptoms associated with seropositivity were analyzed by multiple correspondence analysis, antibody concentrations by multiple linear regression.

resultsTotal of 3608 individual were invited and 1960 recruited from May 8 to July 31, 2020. Seroprevalence was 1.5% (95% confidence interval (CI) 0.9-2.5) and 6.3% (95% CI 5.0-7.9), infection fatality rate 0.1% (95% CI 0.0-0.2) and 1.3% (95% CI 0.4-2.1) in Tallinn and Saaremaa, respectively. Of seropositive subjects 19.2% (14/73) had acute respiratory illness. Fever, diarrhea and the absence of cough and runny nose were associated with seropositivity in individuals aged 50 or more years. IgG, but not neutralizing antibodies concentrations were higher if fever, difficulty breathing, shortness of breath, chest pain or diarrhea was present, or hospitalization required.

conclusionSimilarly to other European countries the seroprevalence of SARS-CoV-2 in Estonia was low even in the hotspot region Saaremaa suggesting that majority of population is susceptible to SARS-CoV-2. Focusing only on respiratory symptoms may delay accurate diagnosis of SARS-CoV-2 infection.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralEstoniaHumansImmunoglobulin GPrevalenceSeroepidemiologic StudiesAntibodies, ViralImmunoglobulin GCOVID-19IggInfection fatality rateSARS-CoV-2SeroprevalenceSymptoms

Identifiers

PMID34393019
PMCPMC8339569
OpenAlexW3190258489

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.