Evidence map›Paper›PMID 38728305›Full record

ArticlePloS one2024

SARS-CoV-2 clade dynamics and their associations with hospitalisations during the first two years of the COVID-19 pandemic.

Taavi Päll, Aare Abroi, Radko Avi, Heiki Niglas, Arina Shablinskaja, Merit Pauskar, Ene-Ly Jõgeda, Hiie Soeorg, Eveli Kallas, Andrio Lahesaare and 25 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

35 authors.

Taavi PällDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0001-7606-675X
Aare AbroiFaculty of Science and Technology, Institute of Technology, University of Tartu, Tartu, Estonia.ORCID 0000-0001-5644-8080
Radko AviDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Heiki NiglasDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.
Arina ShablinskajaDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Merit PauskarDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Ene-Ly JõgedaDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Hiie SoeorgDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Eveli KallasDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Andrio LahesaareSYNLAB Eesti OÜ, Tallinn, Estonia.
Kai TruusaluDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Dagmar HoidmetsDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Olga SadikovaDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.ORCID 0009-0002-6691-0261
Kaspar RatnikSYNLAB Eesti OÜ, Tallinn, Estonia.
Hanna SeppDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.
Liidia DotsenkoDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.
Jevgenia EpšteinDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.
Heleene SuijaDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.
Katrin KaarnaClinical Research Centre, Faculty of Medicine, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
Steven SmitInstitute of Genomics, Faculty of Science and Technology, University of Tartu, Tartu, Estonia.ORCID 0000-0002-3791-635X
Lili MilaniInstitute of Genomics, Faculty of Science and Technology, University of Tartu, Tartu, Estonia.
Mait MetspaluInstitute of Genomics, Faculty of Science and Technology, University of Tartu, Tartu, Estonia.
Ott Eric OopkaupHigh Performance Computing Centre, Faculty of Science and Technology, Institute of Computer Science, University of Tartu, Tartu, Estonia.
Ivar KoppelHigh Performance Computing Centre, Faculty of Science and Technology, Institute of Computer Science, University of Tartu, Tartu, Estonia.
Erik JaanisoInstitute of Computer Science, Faculty of Science and Technology, University of Tartu, Tartu, Estonia.
Ivan KuzminHigh Performance Computing Centre, Faculty of Science and Technology, Institute of Computer Science, University of Tartu, Tartu, Estonia.
Heleri InnoHigh Performance Computing Centre, Faculty of Science and Technology, Institute of Computer Science, University of Tartu, Tartu, Estonia.
Uku RaudvereHigh Performance Computing Centre, Faculty of Science and Technology, Institute of Computer Science, University of Tartu, Tartu, Estonia.
Mari-Anne HärmaDepartment of Communicable Diseases, Health Board, Tallinn, Estonia.
Paul NaaberDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0002-2940-4602
Tuuli ReisbergInstitute of Genomics, Faculty of Science and Technology, University of Tartu, Tartu, Estonia.
Hedi PetersonInstitute of Computer Science, Faculty of Science and Technology, University of Tartu, Tartu, Estonia.
Ulvi Gerst TalasHigh Performance Computing Centre, Faculty of Science and Technology, Institute of Computer Science, University of Tartu, Tartu, Estonia.
Irja LutsarDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Kristi HuikDepartment of Microbiology, Faculty of Medicine, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe COVID-19 pandemic was characterised by rapid waves of disease, carried by the emergence of new and more infectious SARS-CoV-2 virus variants. How the pandemic unfolded in various locations during its first two years has yet to be sufficiently covered. To this end, here we are looking at the circulating SARS-CoV-2 variants, their diversity, and hospitalisation rates in Estonia in the period from March 2000 to March 2022.

methodsWe sequenced a total of 27,550 SARS-CoV-2 samples in Estonia between March 2020 and March 2022. High-quality sequences were genotyped and assigned to Nextstrain clades and Pango lineages. We used regression analysis to determine the dynamics of lineage diversity and the probability of clade-specific hospitalisation stratified by age and sex.

resultsWe successfully sequenced a total of 25,375 SARS-CoV-2 genomes (or 92%), identifying 19 Nextstrain clades and 199 Pango lineages. In 2020 the most prevalent clades were 20B and 20A. The various subsequent waves of infection were driven by 20I (Alpha), 21J (Delta) and Omicron clades 21K and 21L. Lineage diversity via the Shannon index was at its highest during the Delta wave. About 3% of sequenced SARS-CoV-2 samples came from hospitalised individuals. Hospitalisation increased markedly with age in the over-forties, and was negligible in the under-forties. Vaccination decreased the odds of hospitalisation in over-forties. The effect of vaccination on hospitalisation rates was strongly dependent upon age but was clade-independent. People who were infected with Omicron clades had a lower hospitalisation likelihood in age groups of forty and over than was the case with pre-Omicron clades regardless of vaccination status.

conclusionsCOVID-19 disease waves in Estonia were driven by the Alpha, Delta, and Omicron clades. Omicron clades were associated with a substantially lower hospitalisation probability than pre-Omicron clades. The protective effect of vaccination in reducing hospitalisation likelihood was independent of the involved clade.

Indexed as

COVID-19HospitalizationSARS-CoV-2AdolescentAdultAgedAged, 80 and overChildChild, PreschoolEstoniaFemaleGenome, ViralHumansInfantMaleMiddle Aged

Identifiers

PMID38728305
PMCPMC11086870

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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.