Evidence map›Paper›PMID 32562276›Full record

ReviewBritish journal of pharmacology2020

Statins: Could an old friend help in the fight against COVID-19?

Raul R Rodrigues-Diez, Antonio Tejera-Muñoz, Laura Marquez-Exposito, Sandra Rayego-Mateos, Laura Santos Sanchez, Vanessa Marchant, Lucía Tejedor Santamaria, Adrian M Ramos, Alberto Ortiz, Jesus Egido and 1 more

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 5 pooled it
22.5field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 5 syntheses or guidelines pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Statin and outcomes of coronavirus disease 2019 (COVID-19): A systematic review, meta-analysis, and meta-regression.Nutrition, metabolism, and cardiovascular diseases : NMCD · 2021 · on this map
    Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Review
  8. Article
  9. NLRP3 Inflammasomes: Dual Function in Infectious Diseases.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
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  17. Regulation and functions of the NLRP3 inflammasome in RNA virus infection.Frontiers in cellular and infection microbiology · 2023
    Review
  18. Article
  19. Review
  20. Article

13 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 1 country.

Raul R Rodrigues-DiezCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.ORCID 0000-0002-2456-6709
Antonio Tejera-MuñozCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.ORCID 0000-0002-7954-5753
Laura Marquez-ExpositoCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.ORCID 0000-0003-4812-1939
Sandra Rayego-MateosRed de Investigación Renal (REDINREN), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0001-6874-2359
Laura Santos SanchezCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.
Vanessa MarchantCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.ORCID 0000-0002-2767-0229
Lucía Tejedor SantamariaCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.
Adrian M RamosRed de Investigación Renal (REDINREN), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0003-2718-3591
Alberto OrtizRed de Investigación Renal (REDINREN), Instituto de Salud Carlos III, Madrid, Spain.ORCID 0000-0002-9805-9523
Jesus EgidoRenal, Vascular and Diabetes Research Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz Universidad Autónoma, Madrid, Spain.ORCID 0000-0001-6321-2666
Marta Ruiz-OrtegaCellular and Molecular Biology in Renal and Vascular Pathology Laboratory, Fundación Instituto de Investigación Sanitaria-Fundación Jiménez Díaz-Universidad Autónoma Madrid, Madrid, Spain.ORCID 0000-0002-1495-6535
Instituto de Salud Carlos III · ESCentro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ES

Funding

ANALYSIS OF THC IN URINE USING A SIMPLIFIED IMMUNOASSAYR43DA003751 · NIDA · GENESIS LABS, INC. · PI DAY, ALAN R · 1985 to 1985
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Comunidad de Madrid B2017/BMD-3686Comunidad de Madrid B2017/BMD-3751Fondos FEDER European UnionH2020 Marie Skłodowska-Curie ActionsH2020 Marie Skłodowska-Curie Actions 812699Instituto de Salud Carlos III CD19/00021Instituto de Salud Carlos III PI17/00119Instituto de Salud Carlos III PI17/01495Instituto de Salud Carlos III PI18/01133Instituto de Salud Carlos III PI19/00815Ministerio de Economía y Competitividad AC18/00064Ministerio de Economía y Competitividad AC18/00071Ministerio de Economía y Competitividad DTS17/00203Ministerio de Economía y Competitividad DTS18/00032Ministerio de Economía y Competitividad DTS19/00093Ministerio de Economía y Competitividad EIN2019-103294Ministry of Economy and Competitiveness AC18/00064Ministry of Economy and Competitiveness AC18/00071Ministry of Economy and Competitiveness DTS17/00203Ministry of Economy and Competitiveness DTS18/00032Ministry of Economy and Competitiveness DTS19/00093Ministry of Economy and Competitiveness EIN2019-103294
6 · The paper itself

Abstract

The COVID-19 pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has overwhelmed healthcare systems requiring the rapid development of treatments, at least, to reduce COVID-19 severity. Drug repurposing offers a fast track. Here, we discuss the potential beneficial effects of statins in COVID-19 patients based on evidence that they may target virus receptors, replication, degradation, and downstream responses in infected cells, addressing both basic research and epidemiological information. Briefly, statins could modulate virus entry, acting on the SARS-CoV-2 receptors, ACE2 and CD147, and/or lipid rafts engagement. Statins, by inducing autophagy activation, could regulate virus replication or degradation, exerting protective effects. The well-known anti-inflammatory properties of statins, by blocking several molecular mechanisms, including NF-κB and NLRP3 inflammasomes, could limit the "cytokine storm" in severe COVID-19 patients which is linked to fatal outcome. Finally, statin moderation of coagulation response activation may also contribute to improving COVID-19 outcomes. LINKED ARTICLES: This article is part of a themed issue on The Pharmacology of COVID-19. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v177.21/issuetoc.

Indexed as

AnimalsBetacoronavirusCoronavirus InfectionsCOVID-19COVID-19 Drug TreatmentCytokinesDrug RepositioningHumansHydroxymethylglutaryl-CoA Reductase InhibitorsPandemicsPneumonia, ViralSARS-CoV-2Virus InternalizationCytokinesHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID32562276
PMCPMC7323198
OpenAlexW3035860713

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.