Evidence map›Paper›PMID 33676010›Full record

ArticleInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2021

Impact of I/D polymorphism of angiotensin-converting enzyme 1 (ACE1) gene on the severity of COVID-19 patients.

Sushma Verma, Mohammad Abbas, Shrikant Verma, Faizan Haider Khan, Syed Tasleem Raza, Zeba Siddiqi, Israr Ahmad, Farzana Mahdi

Open access · greenAbstract read
In one paragraph

Article in Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 8 pooled it
5.2field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 8 syntheses or guidelines pooled it, 88 citations in OpenAlex.

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  8. Frontiers in genetics · 2022
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  9. Article
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  16. Article
  17. Blood ACE2 Protein Level Correlates with COVID-19 Severity.International journal of molecular sciences · 2023
    Article
  18. Autoimmunity in sarcoidosis: the tip of the Iceberg.Clinical and experimental medicine · 2023
    Article
  19. Article
  20. The effect of ACE2 receptor, IFN-γ, and TNF-α polymorphisms on the severity and prognosis of the disease in SARS-CoV-2 infection.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2023
    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

8 authors at 2 institutions in 2 countries.

Sushma VermaDepartment of Personalized and Molecular Medicine, Era University, Lucknow 226003, Uttar Pradesh, India.
Mohammad AbbasDepartment of Personalized and Molecular Medicine, Era University, Lucknow 226003, Uttar Pradesh, India; Department of Microbiology, Era University, Lucknow 226003, Uttar Pradesh, India.
Shrikant VermaDepartment of Personalized and Molecular Medicine, Era University, Lucknow 226003, Uttar Pradesh, India.
Faizan Haider KhanLambe Institute for Translational Research, Discipline of Pathology, School of Medicine, National University of Ireland Galway (NUIG), Galway, Ireland.
Syed Tasleem RazaDepartment of Biochemistry, Eras Lucknow Medical College and Hospital, Era University, Lucknow 226003, Uttar Pradesh, India.
Zeba SiddiqiDepartment of Medicine, Eras Lucknow Medical College and Hospital, Era University, Lucknow 226003, Uttar Pradesh, India.
Israr AhmadDepartment of Personalized and Molecular Medicine, Era University, Lucknow 226003, Uttar Pradesh, India.
Farzana MahdiDepartment of Personalized and Molecular Medicine, Era University, Lucknow 226003, Uttar Pradesh, India. Electronic address: farzana.mahdi@gmail.com.
Era's Lucknow Medical College and Hospital · INOllscoil na Gaillimhe – University of Galway · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome corona virus-2 (SARS-CoV-2) has first emerged from China in December 2019 and causes coronavirus induced disease 19 (COVID-19). Since then researchers worldwide have been struggling to detect the possible pathogenesis of this disease. COVID-19 showed a wide range of clinical behavior from asymptomatic to severe acute respiratory disease syndrome. However, the etiology of susceptibility to severe lung injury is not yet fully understood. Angiotensin-converting enzyme1 (ACE1) convert angiotensin I into Angiotensin II that was further metabolized by ACE 2 (ACE2). The binding ACE2 receptor to SARS-CoV-2 facilitate its enter into the host cell. The interaction and imbalance between ACE1 and ACE2 play a crucial role in the pathogenesis of lung injury. Thus, the aim of this study was to investigate the association of ACE1 I/D polymorphism with severity of Covid-19. The study included RT-PCR confirmed 269 cases of Covid-19. All cases were genotyped for ACE1 I/D polymorphism using polymerase chain reaction and followed by statistical analysis (SPSS, version 15.0). We found that ACE1 DD genotype, frequency of D allele, older age (≥46 years), unmarried status, and presence of diabetes and hypertension were significantly higher in severe COVID-19 patient. ACE1 ID genotype was significantly independently associated with high socio-economic COVID-19 patients (OR: 2.48, 95% CI: 1.331-4.609). These data suggest that the ACE1 genotype may impact the incidence and clinical outcome of COVID-19 and serve as a predictive marker for COVID-19 risk and severity.

Indexed as

Amino Acid SubstitutionGenetic Predisposition to DiseasePolymorphism, GeneticAdultAgedAge FactorsAllelesAngiotensin-Converting Enzyme 2Aspartic AcidAsymptomatic DiseasesComorbidityCOVID-19Diabetes MellitusFemaleGene Expression RegulationGene FrequencyACE2 protein, humanACE protein, humanAngiotensin-Converting Enzyme 2Aspartic AcidIsoleucinePeptidyl-Dipeptidase AACE I/D polymorphismADRSCovid-19RT-PCRSARS-COV2

Identifiers

PMID33676010
PMCPMC7929788
OpenAlexW3133783226

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.