Evidence map›Paper›PMID 37526809›Full record

ArticleAngiogenesis2024

VEGF-A plasma levels are associated with impaired DLCO and radiological sequelae in long COVID patients.

Aurélien Philippe, Sven Günther, Jeanne Rancic, Pauline Cavagna, Bertrand Renaud, Nicolas Gendron, Elie Mousseaux, Thông Hua-Huy, Guillaume Reverdito, Benjamin Planquette and 5 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Angiogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07089719 (Bevacizumab in Post-acute Sequelae of COVID-19), which is not on this map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
5.8field-weighted citation impact, top 3% 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.

NCT07089719 phase2not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Bevacizumab in Post-acute Sequelae of COVID-19 : Efficacy and Safety (Pilot Study)

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2025 to 2028Enrolled21ConditionsDyspnea Caused by 2019-nCoVArmsBevacizumab Injection
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  3. Blood Biomarkers of Long COVID: A Systematic Review.Molecular diagnosis & therapy · 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 1 country.

Aurélien Philippe *University Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Sven Günther *University Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Jeanne RancicUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Pauline CavagnaPharmacy Department, Pitié-Salpêtrière Hospital, AP-HP Sorbonne University, Paris, France.
Bertrand RenaudUnité d'Explorations Fonctionnelles Respiratoires et du Sommeil, AP-HP, Georges Pompidou European Hospital, 75015, Paris, France.
Nicolas GendronUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Elie MousseauxParis-Cardiovascular Research Center INSERM 970, Université de Paris, Paris, France.
Thông Hua-HuyUnité d'Explorations Fonctionnelles Respiratoires et du Sommeil, AP-HP, Georges Pompidou European Hospital, 75015, Paris, France.
Guillaume ReverditoParis-Cardiovascular Research Center INSERM 970, Université de Paris, Paris, France.
Benjamin PlanquetteUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Olivier SanchezUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Pascale GaussemUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
Dominique SalmonInfectious Diseases and Immunology Department, AP-HP. Centre, Université Paris Cité, Hôtel-Dieu Hospital, 75004, Paris, France.
Jean-Luc DiehlUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France.
David M SmadjaUniversity Paris Cité, Innovative Therapies in Hemostasis, INSERM, 75006, Paris, France. david.smadja@aphp.fr.
Assistance Publique – Hôpitaux de Paris · FRUniversité Paris Cité · FRHôpital Européen Georges-Pompidou · FRSorbonne Paris Cité · FRInserm · FRParis Cardiovascular Research Center · FR

Funding

ANR and Fondation de France SARCODO Flash CovidMécénat Crédit Agricole Ile de France programme jeune talent
6 · The paper itself

Abstract

backgroundLong COVID, also known as post-acute sequelae of COVID-19 (PASC), is characterized by persistent clinical symptoms following COVID-19.

objectiveTo correlate biomarkers of endothelial dysfunction with persistent clinical symptoms and pulmonary function defects at distance from COVID-19.

methodsConsecutive patients with long COVID-19 suspicion were enrolled. A panel of endothelial biomarkers was measured in each patient during clinical evaluation and pulmonary function test (PFT).

resultsThe study included 137 PASC patients, mostly male (68%), with a median age of 55 years. A total of 194 PFTs were performed between months 3 and 24 after an episode of SARS-CoV-2 infection. We compared biomarkers evaluated in PASC patients with 20 healthy volunteers (HVs) and acute hospitalized COVID-19 patients (n = 88). The study found that angiogenesis-related biomarkers and von Willebrand factor (VWF) levels were increased in PASC patients compared to HVs without increased inflammatory or platelet activation markers. Moreover, VEGF-A and VWF were associated with persistent lung CT scan lesions and impaired diffusing capacity of the lungs for carbon monoxide (DLCO) measurement. By employing a Cox proportional hazards model adjusted for age, sex, and body mass index, we further confirmed the accuracy of VEGF-A and VWF. Following adjustment, VEGF-A emerged as the most significant predictive factor associated with persistent lung CT scan lesions and impaired DLCO measurement.

conclusionVEGF-A is a relevant predictive factor for DLCO impairment and radiological sequelae in PASC. Beyond being a biomarker, we hypothesize that the persistence of angiogenic disorders may contribute to long COVID symptoms.

Indexed as

COVID-19Post-Acute COVID-19 SyndromeBiomarkersDisease ProgressionFemaleHumansMaleMiddle AgedSARS-CoV-2Vascular Endothelial Growth Factor Avon Willebrand FactorBiomarkersVascular Endothelial Growth Factor Avon Willebrand FactorAngiogenesisCOVID-19DLCOPost-acute sequelae of SARS-CoV-2 infectionSARS-CoV-2VEGF-A

Identifiers

PMID37526809
OpenAlexW4385442652

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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.