Evidence map›Paper›PMID 42919319›Full record

Observational studyGenome medicine2026

Psychiatric genetic liability is associated with the severity of COVID-19 and other acute respiratory infections: an observational study across five Northern European countries.

Kadri Kõiv, Ragna Bugge Askeland, Lea Arregui Nordahl Christoffersen, Ingibjörg Magnúsdóttir, Daniel McCartney, Ole A Andreassen, Thor Aspelund, Sofiya Babok, Mie Topholm Bruun, Archie Campbell and 22 more

Abstract readObservational Study
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In one paragraph

Observational study in Genome medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

32 authors.

Kadri Kõiv *Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia. kadri.koiv@ut.ee.ORCID https://orcid.org/0000-0001-5286-2014
Ragna Bugge Askeland *PsychGen Centre for Genetic Epidemiology and Mental Health, Norwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0000-0002-7465-0634
Lea Arregui Nordahl Christoffersen *Institute of Biological Psychiatry, Mental Health Services, Amager and Hvidovre Hospital, Copenhagen University Hospital, Roskilde, Denmark.ORCID http://orcid.org/0000-0002-5816-6324
Ingibjörg Magnúsdóttir *Centre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-1983-6049
Daniel McCartney *Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK.ORCID http://orcid.org/0000-0003-3242-0360
Ole A AndreassenNORMENT Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.ORCID http://orcid.org/0000-0002-4461-3568
Thor AspelundCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-7998-5433
Sofiya BabokEstonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0009-0003-1470-7576
Mie Topholm BruunDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark.ORCID http://orcid.org/0000-0002-8819-5388
Archie CampbellCentre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital, Edinburgh, UK.ORCID http://orcid.org/0000-0003-0198-5078
Elizabeth C CorfieldPsychGen Centre for Genetic Epidemiology and Mental Health, Norwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0000-0002-0119-157X
DBDS Genetic Consortium
Maria DidriksenDepartment of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-4856-496X
Christian ErikstrupDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-6551-6647
Estonian Biobank Research Team
Arna HauksdóttirCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-4253-1059
Jóhanna JakobsdóttirCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-8019-9683
Bitten Aagaard JensenDepartment of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.
Isabella LoftDepartment of Clinical Immunology, Zealand University Hospital, Koege, Denmark.ORCID http://orcid.org/0000-0002-4853-1463
Reedik MägiEstonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0002-2964-6011
Dorte Helenius MikkelsenInstitute of Biological Psychiatry, Mental Health Services, Amager and Hvidovre Hospital, Copenhagen University Hospital, Roskilde, Denmark.ORCID http://orcid.org/0000-0002-7360-4812
Sisse Rye OstrowskiDepartment of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5288-3851
Johanne Hagen PettersenPsychGen Centre for Genetic Epidemiology and Mental Health, Norwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0009-0004-4546-9037
Liam QuinnDepartment of Clinical Immunology, Zealand University Hospital, Koege, Denmark.ORCID http://orcid.org/0000-0002-3597-2948
Erik SørensenDepartment of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-5002-9077
Edda Bjork ThordardottirCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0003-3775-9611
Yue WangCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-0349-5681
Thomas WergeInstitute of Biological Psychiatry, Mental Health Services, Amager and Hvidovre Hospital, Copenhagen University Hospital, Roskilde, Denmark.ORCID http://orcid.org/0000-0003-1829-0766
Helga Ask *PsychGen Centre for Genetic Epidemiology and Mental Health, Norwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0000-0003-0149-5319
Ole Birger Vesterager Pedersen *Department of Clinical Immunology, Zealand University Hospital, Koege, Denmark.ORCID http://orcid.org/0000-0003-2312-5976
Unnur Anna ValdimarsdóttirCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.ORCID http://orcid.org/0000-0001-5382-946X
Kelli LehtoEstonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia. kelli.lehto@ut.ee.ORCID http://orcid.org/0000-0003-2735-7643

Funding

Estonian Ministry of Education and Research, Estonian Centre of Excellence for Well-Being Sciences TK218Estonian Research Council PSG615Estonian Research Council, NordForsk 105668EU Horizon2020 CoMorMent, 847776NordForsk 156298NordForsk COVIDMENT, 105668 and 138929Research Council of Norway 248983 and 324620
6 · The paper itself

Abstract

backgroundPre-existing psychiatric disorders have been associated with the severity of acute respiratory infections, including COVID-19, particularly in hospitalized populations. However, the underlying mechanisms, especially in community-based populations, remain unknown, limiting preparedness for future pandemics. We investigated the role of genetic liability for psychiatric disorders and related traits in COVID-19 and other respiratory infection severity among individuals reporting SARS-CoV-2 testing and available respiratory symptom data.

methodsWe included population-based cohort data from Denmark, Estonia, Iceland, Norway, and the United Kingdom (N = 78,507; 62% female; 41% SARS-CoV-2-positive; May 2020-March 2023). Respiratory infection severity was defined by self-reported days bedridden and an eleven-symptom composite score during the acute illness phase. Polygenic scores (PGSs) for eight psychiatric disorders and the personality trait neuroticism indexed genetic liability. Meta-analysed estimates from stepwise-adjusted regression analyses controlling for education, lifestyle, and psychiatric and somatic diagnosis history were used to assess associations between PGSs and acute respiratory infection severity, stratified by COVID-19 status.

resultsHigher genetic liability to insomnia, major depression (MD), and neuroticism was consistently associated with longer time bedridden (relative risk ratios per 1 SD change in PGS: 1.07-1.14, 95% confidence intervals [CIs]: 1.03-1.21) and more symptoms (incident rate ratios [IRRs]: 1.02-1.04, 95% CIs: 1.01-1.05) due to COVID-19. PGSs for insomnia, MD, neuroticism, anxiety disorder, bipolar disorder, and schizophrenia were also linked to higher non-COVID-19 symptom count (IRRs: 1.01-1.05, 95% CIs: 1.00-1.07). These associations remained robust after adjustment for lifestyle, education and medical comorbidities. Individuals in the highest MD PGS decile reported 20% more symptoms in non-COVID-19 illness and 10% more in COVID-19 compared with the bottom decile. No consistent associations were detected with attention-deficit/hyperactivity disorder, alcohol dependence and post-traumatic stress disorder. No genetic link was observed with ischaemic heart disease or type 2 diabetes.

conclusionsShared genetics may contribute to the link between psychiatric conditions and respiratory infection severity in community settings. Our results underscore the role of psychiatric genetic liability, beyond diagnosed psychiatric disorders, in contributing to both COVID-19 and other respiratory infection severity. These findings provide insights that may improve future risk stratification and public health strategies targeting respiratory viruses.

Indexed as

COVID-19Genetic Predisposition to DiseaseMental DisordersRespiratory Tract InfectionsAdultEuropeFemaleGenetic Risk ScoreHumansMaleMiddle AgedMultifactorial InheritanceSARS-CoV-2Severity of Illness IndexAcute respiratory infectionAcute respiratory infection symptomsCommunity samplesCOVID-19Genetic predispositionMental healthPolygenic scoresPsychiatric disorders

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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.