Evidence map›Paper›PMID 33614744›Full record

ReviewFrontiers in cardiovascular medicine2020

Why Is COVID-19 More Severe in Patients With Diabetes? The Role of Angiotensin-Converting Enzyme 2, Endothelial Dysfunction and the Immunoinflammatory System.

Jacob Roberts, Antonia L Pritchard, Andrew T Treweeke, Adriano G Rossi, Nicole Brace, Paul Cahill, Sandra M MacRury, Jun Wei, Ian L Megson

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Pre-pandemic diabetes and risk of long COVID: longitudinal evidence.Journal of diabetes and metabolic disorders · 2025
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  16. Observational
  17. Atypical clinical features of post COVID-19 mucormycosis: A case series.Clinical and experimental dental research · 2023
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  18. Article
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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 3 institutions in 2 countries.

Jacob RobertsInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
Antonia L PritchardInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
Andrew T TreweekeInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
Adriano G RossiCentre for Inflammation Research, University of Edinburgh, Edinburgh, United Kingdom.
Nicole BraceInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
Paul CahillSchool of Biotechnology, Dublin City University, Dublin, Ireland.
Sandra M MacRuryInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
Jun WeiInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
Ian L MegsonInstitute for Health Research and Innovation, University of the Highlands and Islands, Inverness, United Kingdom.
University of the Highlands and Islands · GBDublin City University · IEUniversity of Edinburgh · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meta-analyses have indicated that individuals with type 1 or type 2 diabetes are at increased risk of suffering a severe form of COVID-19 and have a higher mortality rate than the non-diabetic population. Patients with diabetes have chronic, low-level systemic inflammation, which results in global cellular dysfunction underlying the wide variety of symptoms associated with the disease, including an increased risk of respiratory infection. While the increased severity of COVID-19 amongst patients with diabetes is not yet fully understood, the common features associated with both diseases are dysregulated immune and inflammatory responses. An additional key player in COVID-19 is the enzyme, angiotensin-converting enzyme 2 (ACE2), which is essential for adhesion and uptake of virus into cells prior to replication. Changes to the expression of ACE2 in diabetes have been documented, but they vary across different organs and the importance of such changes on COVID-19 severity are still under investigation. This review will examine and summarise existing data on how immune and inflammatory processes interplay with the pathogenesis of COVID-19, with a particular focus on the impacts that diabetes, endothelial dysfunction and the expression dynamics of ACE2 have on the disease severity.

Indexed as

angiotensin converting enzyme-2COVID-19diabetesendotheliumimmune responseinflammationoxidative stressSARS– CoV– 2

Identifiers

PMID33614744
PMCPMC7886785
OpenAlexW3126650156

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.