Evidence map›Paper›PMID 34097193›Full record

ReviewCardiovascular drugs and therapy2022

Is the Endothelium the Missing Link in the Pathophysiology and Treatment of COVID-19 Complications?

Pedro Castro, Marta Palomo, Ana Belen Moreno-Castaño, Sara Fernández, Sergi Torramadé-Moix, Georgina Pascual, Julia Martinez-Sanchez, Edward Richardson, Adrián Téllez, Josep M Nicolas and 5 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Cardiovascular drugs and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

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  10. Serum from COVID-19 patients promotes endothelial cell dysfunction through protease-activated receptor 2.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
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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

15 authors at 6 institutions in 2 countries.

Pedro CastroMedical Intensive Care Unit, Hospital Clinic, Barcelona, Spain.
Marta PalomoJosep Carreras Leukaemia Research Institute, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Ana Belen Moreno-CastañoBarcelona Endothelium Team, Barcelona, Spain.
Sara FernándezMedical Intensive Care Unit, Hospital Clinic, Barcelona, Spain.
Sergi Torramadé-MoixIDIBAPS, Barcelona, Spain.
Georgina PascualArrels Centre Dental, Badalona, Spain.
Julia Martinez-SanchezJosep Carreras Leukaemia Research Institute, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Edward RichardsonFrank H. Netter M.D. School of Medicine At, Quinnipiac University, North Haven, CT, USA.
Adrián TéllezMedical Intensive Care Unit, Hospital Clinic, Barcelona, Spain.
Josep M NicolasMedical Intensive Care Unit, Hospital Clinic, Barcelona, Spain.
Enric CarrerasJosep Carreras Leukaemia Research Institute, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Paul G RichardsonJerome Lipper Multiple Myeloma Center, Division of Hematologic Malignancy, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Juan José BadimonCardiology Department, Cardiovascular Institute, Mount Sinai Hospital, New York, NY, USA.
Gines EscolarSchool of Medicine, University of Barcelona, Barcelona, Spain.
Maribel Diaz-RicartSchool of Medicine, University of Barcelona, Barcelona, Spain. mdiaz@clinic.cat.ORCID 0000-0003-1122-0052
Hospital Clínic de Barcelona · ESJosep Carreras Leukaemia Research Institute · ESBadalona Serveis Assistencials · ESHarvard University · USMount Sinai Hospital · USYale University · US

Funding

Bristol-Myers Squibb ERISTA15Fundació Clínic HCB/2020/0401Fundació la Marató de TV3 202026-10Generalitat de Catalunya 2017-SGR671Instituto de Salud Carlos III PI19/00888Jazz Pharmaceuticals IST-16-10355José Carreras Leukämie-Stiftung 03R/2019
6 · The paper itself

Abstract

Patients with COVID-19 present a wide spectrum of disease severity, from asymptomatic cases in the majority to serious disease leading to critical care and even death. Clinically, four different scenarios occur within the typical disease timeline: first, an incubation and asymptomatic period; second, a stage with mild symptoms due mainly to the virus itself; third, in up to 20% of the patients, a stage with severe symptoms where a hyperinflammatory response with a cytokine storm driven by host immunity induces acute respiratory distress syndrome; and finally, a post-acute sequelae (PASC) phase, which present symptoms that can range from mild or annoying to actually quite incapacitating. Although the most common manifestation is acute respiratory failure of the lungs, other organs are also frequently involved. The clinical manifestations of the COVID-19 infection support a key role for endothelial dysfunction in the pathobiology of this condition. The virus enters into the organism via its interaction with angiotensin-converting enzyme 2-receptor that is present prominently in the alveoli, but also in endothelial cells, which can be directly infected by the virus. Cytokine release syndrome can also drive endothelial damage independently. Consequently, a distinctive feature of SARS-CoV-2 infection is vascular harm, with severe endothelial injury, widespread thrombosis, microangiopathy, and neo-angiogenesis in response to endothelial damage. Therefore, endothelial dysfunction seems to be the pathophysiological substrate for severe COVID-19 complications. Biomarkers of endothelial injury could constitute strong indicators of disease progression and severity. In addition, the endothelium could represent a very attractive target to both prevent and treat these complications. To establish an adequate therapy, the underlying pathophysiology and corresponding clinical stage should be clearly identified. In this review, the clinical features of COVID-19, the central role of the endothelium in COVID-19 and in other pathologies, and the potential of specific therapies aimed at protecting the endothelium in COVID-19 patients are addressed.

Indexed as

COVID-19Vascular DiseasesCytokine Release SyndromeEndothelial CellsEndotheliumEndothelium, VascularHumansSARS-CoV-2CoagulopathyComplement systemCOVID-19COVID-19 therapiesEndothelial protectionEndotheliopathy

Identifiers

PMID34097193
PMCPMC8181544
OpenAlexW3167488394

What OpenQuestion holds

Textmetadata
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.