Evidence map›Paper›PMID 38374351›Full record

ArticleCommunications biology2024

Clonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2.

Luis A Pérez-Jurado, Alejandro Cáceres, Laura Balagué-Dobón, Tonu Esko, Miguel López de Heredia, Inés Quintela, Raquel Cruz, Pablo Lapunzina, Ángel Carracedo, SCOURGE Cohort Group and 1 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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  7. Sex differences in disease: sex chromosome and immunity.Journal of translational medicine · 2024
    Review
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

11 authors at 20 institutions in 10 countries.

Luis A Pérez-Jurado *Genetics Unit, Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona, Spain. luis.perez@upf.edu.ORCID 0000-0002-1988-3005
Alejandro Cáceres *Barcelona Institute for Global Health (ISGlobal), Barcelona, Spain.ORCID 0000-0001-8551-6695
Laura Balagué-DobónBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain.ORCID 0000-0003-3869-9737
Tonu EskoEstonian Genome Science Centre, University of Tartu, Tartu, Estonia.
Miguel López de HerediaCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Barcelona, Spain.ORCID 0000-0003-2826-9565
Inés QuintelaCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Barcelona, Spain.
Raquel CruzCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Barcelona, Spain.ORCID 0000-0002-6964-8898
Pablo LapunzinaCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Barcelona, Spain.ORCID 0000-0002-6324-4825
Ángel CarracedoCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Barcelona, Spain.
SCOURGE Cohort Group
Juan R GonzálezBarcelona Institute for Global Health (ISGlobal), Barcelona, Spain. juanr.gonzalez@isglobal.org.ORCID 0000-0003-3267-2146
Instituto de Salud Carlos III · ESHospital Universitario La Paz · ESUniversidade de Brasília · BRUniversidad de Salamanca · ESUniversidade Federal do Rio Grande do Norte · BRHospital Universitario Fundación Jiménez Díaz · ESUniversidad Complutense de Madrid · ESUniversitat Autònoma de Barcelona · ESUniversidade de Santiago de Compostela · ESUniversidad Simón Bolívar · COUniversidad de Los Andes · COUniversidad de Cantabria · ESBioCruces Health research Institute · ESSpanish National Cancer Research Centre · ESUniversidad Francisco de Vitoria · ESHospital Universitario Virgen de las Nieves · ESInstituto Murciano de Investigación Biosanitaria · ESMarqués de Valdecilla University Hospital · ESUniversidad de Guadalajara · MXComplejo Asistencial Universitario de Palencia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, COVID-19) had an estimated overall case fatality ratio of 1.38% (pre-vaccination), being 53% higher in males and increasing exponentially with age. Among 9578 individuals diagnosed with COVID-19 in the SCOURGE study, we found 133 cases (1.42%) with detectable clonal mosaicism for chromosome alterations (mCA) and 226 males (5.08%) with acquired loss of chromosome Y (LOY). Individuals with clonal mosaic events (mCA and/or LOY) showed a 54% increase in the risk of COVID-19 lethality. LOY is associated with transcriptomic biomarkers of immune dysfunction, pro-coagulation activity and cardiovascular risk. Interferon-induced genes involved in the initial immune response to SARS-CoV-2 are also down-regulated in LOY. Thus, mCA and LOY underlie at least part of the sex-biased severity and mortality of COVID-19 in aging patients. Given its potential therapeutic and prognostic relevance, evaluation of clonal mosaicism should be implemented as biomarker of COVID-19 severity in elderly people.

Indexed as

COVID-19SARS-CoV-2AgedAgingChromosomes, Human, YHumansMaleMosaicism

Identifiers

PMID38374351
PMCPMC10876565
OpenAlexW4391931142

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.