Evidence map›Paper›PMID 37884975›Full record

ArticleJournal of translational medicine2023

HCG18, LEF1AS1 and lncCEACAM21 as biomarkers of disease severity in the peripheral blood mononuclear cells of COVID-19 patients.

Simona Greco, Alisia Made', Martina Mutoli, Lu Zhang, Santiago Nicolas Piella, Mélanie Vausort, Andrew I Lumley, Antonio Paolo Beltrami, Prashant Kumar Srivastava, Valentina Milani and 9 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 12 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

19 authors at 8 institutions in 5 countries.

Simona Greco *Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, Via Morandi 30, 20097, San Donato Milanese, Milan, Italy. simona.greco@grupposandonato.it.
Alisia Made' *Molecular Cardiology Laboratory, IRCCS Policlinico San Donato, Via Morandi 30, 20097, San Donato Milanese, Milan, Italy.
Martina Mutoli *IRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy.
Lu ZhangBioinformatics Platform, Data Integration and Analysis Unit, Luxembourg Institute of Health, 1445, Strassen, Luxembourg.
Santiago Nicolas PiellaMolecular Cardiology Laboratory, IRCCS Policlinico San Donato, Via Morandi 30, 20097, San Donato Milanese, Milan, Italy.
Mélanie VausortCardiovascular Research Unit, Department of Precision Health, Luxembourg Institute of Health, 1445, Strassen, Luxembourg.
Andrew I LumleyCardiovascular Research Unit, Department of Precision Health, Luxembourg Institute of Health, 1445, Strassen, Luxembourg.
Antonio Paolo BeltramiDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Prashant Kumar SrivastavaNational Heart and Lung Institute, Imperial College London, Hammersmith Campus, London, W12 0NN, England, UK.
Valentina MilaniLaboratory of Biostatistics and Data Management, Scientific Directorate, IRCCS Policlinico San Donato, 20097, San Donato Milanese, Milan, Italy.
Sara BoveriLaboratory of Biostatistics and Data Management, Scientific Directorate, IRCCS Policlinico San Donato, 20097, San Donato Milanese, Milan, Italy.
Marco RanucciDepartment of Cardiovascular Anesthesia and ICU, IRCCS Policlinico San Donato, Via Morandi 30, 20097, San Donato Milanese, Milan, Italy.
Laura Valentina RennaBiobank BioCor, IRCCS-Policlinico San Donato, Via Morandi 30, 20097, San Donato Milanese, Milan, Italy.
Hüseyin FiratFiralis SA, 35 Rue du Fort, 68330, Huningue, France.
Antonino BrunoIRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy.
Gaia SpinettiIRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy.
Costanza EmanueliNational Heart and Lung Institute, Imperial College London, Hammersmith Campus, London, W12 0NN, England, UK. c.emanueli@imperial.ac.uk.
Yvan DevauxCardiovascular Research Unit, Department of Precision Health, Luxembourg Institute of Health, 1445, Strassen, Luxembourg. yvan.devaux@lih.lu.
Fabio MartelliMolecular Cardiology Laboratory, IRCCS Policlinico San Donato, Via Morandi 30, 20097, San Donato Milanese, Milan, Italy. fabio.martelli@grupposandonato.it.ORCID 0000-0002-8624-7738
IRCCS Policlinico San Donato · ITLuxembourg Institute of Health · LUMultiMedica · ITFiralis (France) · FRImperial College London · GBLung Institute · USUniversity of Insubria · ITUniversity of Udine · IT

Funding

British Heart Foundation CH/15/1/31199
6 · The paper itself

Abstract

backgroundEven after 3 years from SARS-CoV-2 identification, COVID-19 is still a persistent and dangerous global infectious disease. Significant improvements in our understanding of the disease pathophysiology have now been achieved. Nonetheless, reliable and accurate biomarkers for the early stratification of COVID-19 severity are still lacking. Long noncoding RNAs (LncRNAs) are ncRNAs longer than 200 nucleotides, regulating the transcription and translation of protein-coding genes and they can be found in the peripheral blood, thus holding a promising biomarker potential. Specifically, peripheral blood mononuclear cells (PBMCs) have emerged as a source of indirect biomarkers mirroring the conditions of tissues: they include monocytes, B and T lymphocytes, and natural killer T cells (NKT), being highly informative for immune-related events.

methodsWe profiled by RNA-Sequencing a panel of 2906 lncRNAs to investigate their modulation in PBMCs of a pilot group of COVID-19 patients, followed by qPCR validation in 111 hospitalized COVID-19 patients.

resultsThe levels of four lncRNAs were found to be decreased in association with COVID-19 mortality and disease severity: HLA Complex Group 18-242 and -244 (HCG18-242 and HCG18-244), Lymphoid Enhancer Binding Factor 1-antisense 1 (LEF1-AS1) and lncCEACAM21 (i.e. ENST00000601116.5, a lncRNA in the CEACAM21 locus). Interestingly, these deregulations were confirmed in an independent patient group of hospitalized patients and by the re-analysis of publicly available single-cell transcriptome datasets. The identified lncRNAs were expressed in all of the PBMC cell types and inversely correlated with the neutrophil/lymphocyte ratio (NLR), an inflammatory marker. In vitro, the expression of LEF1-AS1 and lncCEACAM21 was decreased upon THP-1 monocytes exposure to a relevant stimulus, hypoxia.

conclusionThe identified COVID-19-lncRNAs are proposed as potential innovative biomarkers of COVID-19 severity and mortality.

Indexed as

COVID-19RNA, Long NoncodingBiomarkersHumansLeukocytes, MononuclearPatient AcuitySARS-CoV-2BiomarkersRNA, Long Noncoding

Identifiers

PMID37884975
PMCPMC10605335
OpenAlexW4387966282

What Socratic 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 Socratic graph.