Evidence map›Paper›PMID 32526061›Full record

SynthesisAndrology2021

Targeting the NO-cGMP-PDE5 pathway in COVID-19 infection. The DEDALO project.

Andrea M Isidori, Elisa Giannetta, Riccardo Pofi, Mary A Venneri, Daniele Gianfrilli, Federica Campolo, Claudio M Mastroianni, Andrea Lenzi, Gabriella d'Ettorre

Open access · bronzeAbstract readSystematic Review
In one paragraph

Synthesis in Andrology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

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  16. Pulmonary artery targeted therapy in treatment of COVID-19 related ARDS. Literature review.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2022
    Review
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  19. Interaction betweenPathogens (Basel, Switzerland) · 2021
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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

9 authors at 2 institutions in 1 country.

Andrea M IsidoriDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.ORCID 0000-0002-9037-5417
Elisa GiannettaDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.
Riccardo PofiDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.
Mary A VenneriDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.
Daniele GianfrilliDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.ORCID 0000-0002-2682-8266
Federica CampoloDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.
Claudio M MastroianniDepartment of Public Health and Infectious Diseases, "Sapienza" University of Rome, Policlinico Umberto I of Rome, Rome, Italy.
Andrea LenziDepartment of Experimental Medicine, Sapienza" University of Rome, Rome, Italy.
Gabriella d'EttorreDepartment of Public Health and Infectious Diseases, "Sapienza" University of Rome, Policlinico Umberto I of Rome, Rome, Italy.
Sapienza University of Rome · ITPoliclinico Umberto I · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA pandemic outbreak of COVID-19 has been sweeping the world since December. It begins as a respiratory infection that, mainly in men with diabetes or renal impairment, evolves into a systemic disease, with SARDS, progressive endothelial cell damage, abnormal clotting and impaired cardiovascular and liver function. Some clinical trials are testing biological drugs to limit the immune system dysregulation, "cytokines storm," that causes the systemic complications of COVID-19. The contraindications of these drugs and their cost raise concerns over the implications of their widespread availability.

objectivesNumerous clinical and experimental studies have revealed a role for the nitric oxide (NO)-cyclic GMP-phosphodiesterase type 5 (PDE5) pathway in modulating low-grade inflammation in patients with metabolic diseases, offering cardiovascular protection. PDE5 inhibition favors an anti-inflammatory response by modulating activated T cells, reducing cytokine release, lowering fibrosis, increasing oxygen diffusion, stimulating vascular repair. PDE5 is highly expressed in the lungs, where its inhibition improves pulmonary fibrosis, a complication of severe COVID-19 disease. MATERIALS AND

methodsWe performed a systematic review of all evidence documenting any involvement of the NO-cGMP-PDE5 axis in the pathophysiology of COVID-19, presenting the ongoing clinical trials aimed at modulating this axis, including our own "silDEnafil administration in DiAbetic and dysmetaboLic patients with COVID-19 (DEDALO trial)."

resultsThe reviewed evidence suggests that PDE5 inhibitors could offer a new strategy in managing COVID-19 by (i) counteracting the Ang-II-mediated downregulation of AT-1 receptor; (ii) acting on monocyte switching, thus reducing pro-inflammatory cytokines, interstitial infiltration and the vessel damage responsible for alveolar hemorrhage-necrosis; (iii) inhibiting the transition of endothelial and smooth muscle cells to mesenchymal cells in the pulmonary artery, preventing clotting and thrombotic complications. DISCUSSION AND

conclusionIf the ongoing trials presented herein should provide positive findings, the low cost, wide availability and temperature stability of PDE5 inhibitors could make them a major resource to combat COVID-19 in developing countries.

Indexed as

COVID-19 Drug TreatmentAntiviral AgentsClinical Trials as TopicCOVID-19Cyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5Host-Pathogen InteractionsHumansMolecular Targeted TherapyNitric OxidePhosphodiesterase 5 InhibitorsSARS-CoV-2Signal TransductionTreatment OutcomeAntiviral AgentsCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5Nitric OxidePhosphodiesterase 5 Inhibitorscytokine stormIL-6interstitial pneumoniaPDE5 inhibitorspulmonary fibrosistype 2 diabetes mellitus

Identifiers

PMID32526061
PMCPMC7307129
OpenAlexW3034758467

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.