Evidence map›Paper›PMID 35613127›Full record

ArticlePloS one2022

CMV seropositivity is a potential novel risk factor for severe COVID-19 in non-geriatric patients.

Simone Weber, Victoria Kehl, Johanna Erber, Karolin I Wagner, Ana-Marija Jetzlsperger, Teresa Burrell, Kilian Schober, Philipp Schommers, Max Augustin, Claudia S Crowell and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

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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

18 authors at 7 institutions in 1 country.

Simone WeberInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.
Victoria KehlInstitute for AI and Informatics in Medicine, School of Medicine, Technical University of Munich, Munich, Germany.
Johanna ErberDepartment of Internal Medicine II, University Hospital Rechts Der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
Karolin I WagnerInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.
Ana-Marija JetzlspergerInstitute of Virology, School of Medicine, Technical University of Munich, Munich, Germany.
Teresa BurrellInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.
Kilian SchoberMikrobiologisches Institut-Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Erlangen, Germany.
Philipp SchommersMedical Faculty and University Hospital Cologne, Department I of Internal Medicine, University of Cologne, Cologne, Germany.
Max AugustinMedical Faculty and University Hospital Cologne, Department I of Internal Medicine, University of Cologne, Cologne, Germany.
Claudia S CrowellInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.
Markus GerhardInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.
Christof WinterInstitute of Clinicl Chemistry and Pathobiochemistry, School of Medicine, Technical University of Munich, Munich, Germany.ORCID 0000-0002-0253-9056
Andreas MoosmannGerman Center for Infection Research (DZIF), Munich, Germany.
Christoph D SpinnerDepartment of Internal Medicine II, University Hospital Rechts Der Isar, School of Medicine, Technical University of Munich, Munich, Germany.ORCID 0000-0002-3875-5367
Ulrike ProtzerInstitute of Virology, School of Medicine, Technical University of Munich, Munich, Germany.
Dieter HoffmannInstitute of Virology, School of Medicine, Technical University of Munich, Munich, Germany.
Elvira D'IppolitoInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.
Dirk H BuschInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany.ORCID 0000-0001-8713-093X
Technical University of Munich · DEInstitute of Medical Microbiology and Hygiene · DEGerman Center for Infection Research · DETUM Klinikum · DEUniversity of Cologne · DELMU Klinikum · DEUniversitätsklinikum Erlangen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOVID-19 has so far affected more than 250 million individuals worldwide, causing more than 5 million deaths. Several risk factors for severe disease have been identified, most of which coincide with advanced age. In younger individuals, severe COVID-19 often occurs in the absence of obvious comorbidities. Guided by the finding of cytomegalovirus (CMV)-specific T cells with some cross-reactivity to SARS-CoV-2 in a COVID-19 intensive care unit (ICU) patient, we decided to investigate whether CMV seropositivity is associated with severe or critical COVID-19. Herpes simplex virus (HSV) serostatus was investigated as control.

methodsNational German COVID-19 bio-sample and data banks were used to retrospectively analyze the CMV and HSV serostatus of patients who experienced mild (n = 101), moderate (n = 130) or severe to critical (n = 80) disease by IgG serology. We then investigated the relationship between disease severity and herpesvirus serostatus via statistical models.

resultsNon-geriatric patients (< 60 years) with severe COVID-19 were found to have a very high prevalence of CMV-seropositivity, while CMV status distribution in individuals with mild disease was similar to the prevalence in the German population; interestingly, this was not detectable in older patients. Prediction models support the hypothesis that the CMV serostatus, unlike HSV, might be a strong biomarker in identifying younger individuals with a higher risk of developing severe COVID-19, in particular in absence of other co-morbidities.

conclusionsWe identified 'CMV-seropositivity' as a potential novel risk factor for severe COVID-19 in non-geriatric individuals in the studied cohorts. More mechanistic analyses as well as confirmation of similar findings in cohorts representing the currently most relevant SARS-CoV-2 variants should be performed shortly.

Indexed as

COVID-19Cytomegalovirus InfectionsHerpes SimplexAgedAntibodies, ViralCytomegalovirusHumansRetrospective StudiesRisk FactorsSARS-CoV-2Antibodies, Viral

Identifiers

PMID35613127
PMCPMC9132318
OpenAlexW4281556208

What OpenQuestion holds

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LicenceCC BY
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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.