Evidence map›Paper›PMID 39862311›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2025

Endocan as a marker of endotheliitis in COVID-19 patients: modulation by veno-venous extracorporeal membrane oxygenation, arterial hypertension and previous treatment with renin-angiotensin-aldosterone system inhibitors.

Marta Reina-Couto, David Alves, Carolina Silva-Pereira, Patrícia Pereira-Terra, Sandra Martins, João Bessa, Luísa Teixeira-Santos, Dora Pinho, Manuela Morato, Cláudia Camila Dias and 7 more

Abstract read
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

17 authors.

Marta Reina-Couto *Departamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal. couto.mr@gmail.com.
David Alves *Departamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Carolina Silva-PereiraDepartamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Patrícia Pereira-TerraDepartamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Sandra MartinsServiço de Patologia Clínica, CHUSJ, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
João BessaServiço de Nefrologia, Centro Hospitalar Universitário de Santo António, Largo Prof. Abel Salazar, 4099-001, Porto, Portugal.
Luísa Teixeira-SantosDepartamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Dora PinhoDepartamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Manuela MoratoDepartamento de Ciências do Medicamento, Laboratório de Farmacologia, Faculdade de Farmácia da Universidade do Porto, Rua Jorge Viterbo Ferreira nº 228, 4050-313, Porto, Portugal.
Cláudia Camila DiasDepartamento de Medicina da Comunidade, Informação e Decisão em Saúde, FMUP, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
António SarmentoServiço de Doenças Infecciosas, CHUSJ, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
Margarida TavaresServiço de Doenças Infecciosas, CHUSJ, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
João T GuimarãesServiço de Patologia Clínica, CHUSJ, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
Roberto Roncon-AlbuquerqueServiço de Medicina Intensiva, Centro Hospitalar e Universitário São João (CHUSJ), Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
José-Artur PaivaServiço de Medicina Intensiva, Centro Hospitalar e Universitário São João (CHUSJ), Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
António Albino-Teixeira *Departamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Teresa Sousa *Departamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal. tsousa@med.up.pt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsEndocan has been scarcely explored in COVID-19, especially regarding its modulation by veno-venous extracorporeal membrane oxygenation (VV-ECMO), hypertension or previous renin-angiotensin-aldosterone system (RAAS) inhibitors treatment. We compared endocan and other endotheliitis markers in hospitalized COVID-19 patients and assessed their modulation by VV-ECMO, hypertension and previous RAAS inhibitors treatment. MATERIAL AND

methodsSerum endocan, intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1) and E-selectin were measured in "severe" (n = 27), "critically ill" (n = 17) and "critically ill on VV-ECMO" (n = 17) COVID-19 patients at admission, days 3-4, 5-8 and weekly thereafter, and in controls (n = 23) at a single time point.

resultsAdmission endocan and VCAM-1 were increased in all patients, but "critically ill on VV-ECMO" patients had higher endocan and E-Selectin. Endocan remained elevated throughout hospitalization in all groups. "Severe" and "critically ill" hypertensive patients or previously treated with RAAS inhibitors had higher endocan and/or VCAM-1, but in VV-ECMO patients the raised endocan values seemed unrelated with these factors. Among all COVID-19 hypertensive patients, those with previous RAAS inhibitors treatment had higher endocan.

conclusionsIn our study, endocan stands out as the best marker of endotheliitis in hospitalized COVID-19 patients, being upregulated by VV-ECMO support, hypertension and previous RAAS inhibitor treatment.

Indexed as

COVID-19HypertensionNeoplasm ProteinsProteoglycansAdultAgedAngiotensin-Converting Enzyme InhibitorsBiomarkersE-SelectinFemaleHumansIntercellular Adhesion Molecule-1MaleMiddle AgedRenin-Angiotensin SystemSARS-CoV-2Angiotensin-Converting Enzyme InhibitorsBiomarkersE-SelectinESM1 protein, humanICAM1 protein, humanIntercellular Adhesion Molecule-1Neoplasm ProteinsProteoglycansSELE protein, humanVascular Cell Adhesion Molecule-1COVID-19EndocanEndotheliitisHypertensionRAAS inhibitorsVV-ECMO

Identifiers

PMID39862311
PMCPMC11762693

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.