Evidence map›Paper›PMID 33362575›Full record

ReviewFrontiers in physiology2020

Pathophysiology of SARS-CoV-2 in Lung of Diabetic Patients.

Tales Lyra Oliveira, Igor Santana Melo, Léia Cardoso-Sousa, Igor Andrade Santos, Mohamad Bassim El Zoghbi, Caroline Gusson Shimoura, Renata Pereira Georjutti, Olagide Wagner Castro, Luiz Ricardo Goulart, Ana Carolina Gomes Jardim and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. Vitamin D and COVID-19: An Overview of Recent Evidence.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Review
  9. 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

12 authors.

Tales Lyra OliveiraHeart Institute, Faculty of Medicine, University of São Paulo, São Paulo, Brazil.
Igor Santana MeloInstitute of Biological Sciences and Health, Federal University of Alagoas, Alagoas, Brazil.
Léia Cardoso-SousaDepartment of Physiology, Institute of Biomedical Sciences, Federal University of Uberlândia, Uberlândia, Brazil.
Igor Andrade SantosLaboratory of Virology, Institute of Biomedical Sciences, Federal University of Uberlândia, Uberlândia, Brazil.
Mohamad Bassim El ZoghbiMedical School, Municipal University of São Caetano do Sul, São Paulo, Brazil.
Caroline Gusson ShimouraDepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, United States.
Renata Pereira GeorjuttiDepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, United States.
Olagide Wagner CastroInstitute of Biological Sciences and Health, Federal University of Alagoas, Alagoas, Brazil.
Luiz Ricardo GoulartInstitute of Biotechnology, Federal University of Uberlândia, Uberlândia, Brazil.
Ana Carolina Gomes JardimLaboratory of Virology, Institute of Biomedical Sciences, Federal University of Uberlândia, Uberlândia, Brazil.
Thúlio Marquez CunhaDepartment of Pulmonology, School of Medicine, Federal University of Uberlândia, Uberlândia, Brazil.
Robinson Sabino-SilvaDepartment of Physiology, Institute of Biomedical Sciences, Federal University of Uberlândia, Uberlândia, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Novel coronavirus disease (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Its impact on patients with comorbidities is clearly related to fatality cases, and diabetes has been linked to one of the most important causes of severity and mortality in SARS-CoV-2 infected patients. Substantial research progress has been made on COVID-19 therapeutics; however, effective treatments remain unsatisfactory. This unmet clinical need is robustly associated with the complexity of pathophysiological mechanisms described for COVID-19. Several key lung pathophysiological mechanisms promoted by SARS-CoV-2 have driven the response in normoglycemic and hyperglycemic subjects. There is sufficient evidence that glucose metabolism pathways in the lung are closely tied to bacterial proliferation, inflammation, oxidative stress, and pro-thrombotic responses, which lead to severe clinical outcomes. It is also likely that SARS-CoV-2 proliferation is affected by glucose metabolism of type I and type II cells. This review summarizes the current understanding of pathophysiology of SARS-CoV-2 in the lung of diabetic patients and highlights the changes in clinical outcomes of COVID-19 in normoglycemic and hyperglycemic conditions.

Indexed as

angiotensin-converting enzymebetacoronavirus infectiondiabetes mellituspneumoniaSGLT1

Identifiers

PMID33362575
PMCPMC7758507

What OpenQuestion holds

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Registered trials

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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.