Evidence map›Paper›PMID 32901433›Full record

ArticleJournal of racial and ethnic health disparities2021

Ethnic Prevalence of Angiotensin-Converting Enzyme Deletion (D) Polymorphism and COVID-19 Risk: Rationale for Use of Angiotensin-Converting Enzyme Inhibitors/Angiotensin Receptor Blockers.

Rangaprasad Sarangarajan, Robert Winn, Michael A Kiebish, Chas Bountra, Elder Granger, Niven R Narain

Open access · hybridAbstract read
In one paragraph

Article in Journal of racial and ethnic health disparities, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Polymorphisms in the ACE I/D (Tropical medicine and infectious disease · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Review
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  18. Frontiers in immunology · 2022
    Article
  19. Article
  20. Association Between theFrontiers in medicine · 2022
    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

6 authors at 3 institutions in 3 countries.

Rangaprasad SarangarajanBERG LLC, 500 Old Connecticut Path, Bldg B, 3r Floor, Framingham, MA, 01701, USA. Rangaprasad.Sarangarajan@BergHealth.com.ORCID https://orcid.org/0000-0001-9403-9421
Robert WinnMassey Cancer Center, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Michael A KiebishBERG LLC, 500 Old Connecticut Path, Bldg B, 3r Floor, Framingham, MA, 01701, USA.
Chas BountraCenter for Medicines Discovery, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, OX37DQ, UK.
Elder GrangerBERG LLC, 500 Old Connecticut Path, Bldg B, 3r Floor, Framingham, MA, 01701, USA.
Niven R NarainBERG LLC, 500 Old Connecticut Path, Bldg B, 3r Floor, Framingham, MA, 01701, USA.
Institut Bergonié · FRUniversity of Oxford · GBVirginia Commonwealth University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleHypertension, obesity and diabetes are major risk factors associated with morbidities underlying COVID-19 infections. Regression analysis correlated presence of ACE insertion/deletion (I/D) polymorphism to COVID-19 incidence and mortality. Furthermore, COVID-19 prevalence correlated to allele frequency of angiotensin-converting enzyme (ACE) deletion (D) polymorphism within the European population.

objectiveHomozygous ACE deletion polymorphism is associated with increase in ACE and angiotensin II (Ang-II), sustained levels can result in inflammation, fibrosis and organ damage. The ACE DD polymorphism is also associated with hypertension, acute respiratory distress and diabetic nephropathy, all considered high risk for COVID-19 infection and outcomes. The study objective was to describe a biological framework associating ethnic prevalence of ACE deletion polymorphism to COVID-19 comorbidities providing rationale for therapeutic utility of ACE-I/ARBs to improve outcomes. METHOD AND

resultsThe Allele Frequency Database (ALFRED) was queried for frequency of rs4646994 representing ACE I/D polymorphism. In a total of 349 worldwide population samples, frequency of ACE D allele was higher in European, Asian, and Africans cohorts. In the USA, the frequency of ACE D allele was higher in non-Hispanic Black compared with non-Hispanic White and Mexican Americans.

conclusionCOVID-19 binding mediated reduction/inactivation of ACE-II can increase ACE/Ang-II signalling pathway and related pathologies. The presence of ACE DD polymorphism with COVID-19 infection likely augments ACE/Ang-II activities, increasing severity of COVID-19 morbidities and impacts outcomes. Thus, ethnic prevalence of ACE DD polymorphism can explain in part the severity of COVID-19 morbidity providing rationale for the use of ACE-I/ARBs to improve outcomes.

Indexed as

COVID-19 Drug TreatmentAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsCOVID-19EthnicityGenetic Predisposition to DiseaseHumansPeptidyl-Dipeptidase APolymorphism, GeneticPrevalenceRisk FactorsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsPeptidyl-Dipeptidase AACEAngiotensinCOVID-19EthnicPolymorphism

Identifiers

PMID32901433
PMCPMC7478439
OpenAlexW3084056725

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.