Evidence map›Paper›PMID 33101215›Full record

ReviewFrontiers in endocrinology

Stabilizing Cellular Barriers: Raising the Shields Against COVID-19.

Julia Hanchard, Coral M Capó-Vélez, Kai Deusch, Darcy Lidington, Steffen-Sebastian Bolz

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

5 authors at 2 institutions in 1 country.

Julia HanchardAphaia Pharma AG, Zug, Switzerland.
Coral M Capó-VélezAphaia Pharma AG, Zug, Switzerland.
Kai DeuschAphaia Pharma AG, Zug, Switzerland.
Darcy LidingtonAphaia Pharma AG, Zug, Switzerland.
Steffen-Sebastian BolzAphaia Pharma AG, Zug, Switzerland.
University of Toronto · CATed Rogers Centre for Heart Research · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its clinical manifestation (COVID-19; coronavirus disease 2019) have caused a worldwide health crisis. Disruption of epithelial and endothelial barriers is a key clinical turning point that differentiates patients who are likely to develop severe COVID-19 outcomes: it marks a significant escalation in respiratory symptoms, loss of viral containment and a progression toward multi-organ dysfunction. These barrier mechanisms are independently compromised by known COVID-19 risk factors, including diabetes, obesity and aging: thus, a synergism between these underlying conditions and SARS-CoV-2 mechanisms may explain why these risk factors correlate with more severe outcomes. This review examines the key cellular mechanisms that SARS-CoV-2 and its underlying risk factors utilize to disrupt barrier function. As an outlook, we propose that glucagon-like peptide 1 (GLP-1) may be a therapeutic intervention that can slow COVID-19 progression and improve clinical outcome following SARS-CoV-2 infection. GLP-1 signaling activates barrier-promoting processes that directly oppose the pro-inflammatory mechanisms commandeered by SARS-CoV-2 and its underlying risk factors.

Indexed as

AgingBetacoronavirusCoronavirus InfectionsCOVID-19Diabetes MellitusGlucagon-Like Peptide 1HumansInflammationObesityPandemicsPneumonia, ViralSARS-CoV-2Glucagon-Like Peptide 1acute respiratory and circulatory disruptionendothelial barrier disruptionenteroendocrineglucagon like peptide 1 (GLP-1)immune cellslungtumor necrosis factor converting enzyme (TACE)tumor necrosis factor (TNF)

Identifiers

PMID33101215
PMCPMC7554589
OpenAlexW3091754408

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.