Evidence map›Paper›PMID 32542429›Full record

SynthesisEndocrine2020

Worldwide ACE (I/D) polymorphism may affect COVID-19 recovery rate: an ecological meta-regression.

Naser Hatami, Salma Ahi, Alireza Sadeghinikoo, Mahdi Foroughian, Farshid Javdani, Navid Kalani, Mostafa Fereydoni, Pouyan Keshavarz, Ava Hosseini

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Endocrine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 3 pooled it
1.9field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 3 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Exploring the ethics of genetic prioritisation for COVID-19 vaccines.European journal of human genetics : EJHG · 2022
    Review
  11. Review
  12. Article
  13. Association Between theFrontiers in medicine · 2022
    Article
  14. Host polymorphisms and COVID-19 infection.Advances in clinical chemistry · 2022
    Article
  15. Review
  16. Article
  17. Review
  18. Article
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  20. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Naser HatamiStudent Research Committee, Jahrom University of Medical Sciences, Jahrom, Iran.
Salma AhiResearch Center for Noncommunicable Diseases, Faculty of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran. Salmaahi.61@gmail.com.
Alireza SadeghinikooSports Medicine Center, Oxygen Sports Group, Tehran, Iran.
Mahdi ForoughianDepartment of emergency medicine, Faculty of Medicine, Mashhad University of medical sciences, Mashhad, Iran.
Farshid JavdaniStudent Research Committee, Jahrom University of Medical Sciences, Jahrom, Iran.
Navid KalaniResearch center for social Determinants of Health, Jahrom University of Medical Sciences, Jahrom, Iran.
Mostafa FereydoniStudent Research Committee, Jahrom University of Medical Sciences, Jahrom, Iran.
Pouyan KeshavarzStudent Research Committee, Jahrom University of Medical Sciences, Jahrom, Iran.
Ava HosseiniStudent Research Committee, Jahrom University of Medical Sciences, Jahrom, Iran.
Jahrom University · IRJahrom University of Medical Sciences · IRMashhad University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the emergence of the Novel Coronavirus (2019-nCoV), researchers worldwide have started detecting the probable pathogenesis of the disease. The renin-angiotensin system (RAS) and angiotensin-converting enzymes have received a good deal of attention as possible pathways involved in 2019-nCoV pathogenesis. As the experiments seeking to find potential medications acting on these pathways are being conducted in the early phases, having an ecological worldview on the relationship between the prevalence of COVID-19 disease and the genetic differences in the genes involved in the RAS system could be valuable for the field. In this regard, we conducted a meta-analysis study of the prevalence of ACE (I/D) genotype in countries most affected by the COVID-19. In the meta-analysis, 48,758 healthy subjects from 30 different countries were evaluated in 116 studies, using the Comprehensive Meta-analysis software. The I/D allele frequency ratio was pooled by a random-effect model. The COVID-19 prevalence data of death and recovery rates were evaluated as the latitudes for the meta-regression analysis. Our results demonstrated that with the increase of the I/D allele frequency ratio, the recovery rate significantly increased (point estimate: 0.48, CI 95%: 0.05-0.91, p = 0.027). However, there was no significant difference in the case of death rate (point estimate: 1.74, CI 95%: 4.5-1.04, p = 0.22). This ecological perspective coupled with many limitations does not provide a direct clinical relevance between the COVID-19 and RAS system, but it shows potential pathophysiological associations. Our results raise concerns about ethnic and genetic differences that could affect the effectiveness of the currently investigated RAS-associated medications in different regions.

Indexed as

BetacoronavirusAngiotensin-Converting Enzyme 2Coronavirus InfectionsCOVID-19Gene FrequencyGenetic Predisposition to DiseaseHumansPandemicsPeptidyl-Dipeptidase APneumonia, ViralPolymorphism, GeneticRenin-Angiotensin SystemSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Peptidyl-Dipeptidase A

Identifiers

PMID32542429
PMCPMC7294766
OpenAlexW3034529070

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.