Evidence map›Paper›PMID 35714803›Full record

SynthesisGene2022

The association of COVID-19 severity and susceptibility and genetic risk factors: A systematic review of the literature.

Angela Ishak, Meghana Mehendale, Mousa M AlRawashdeh, Cristina Sestacovschi, Medha Sharath, Krunal Pandav, Sima Marzban

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Gene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Genetic variants inFrontiers in genetics · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Association ofHeliyon · 2024
    Article
  15. Article
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  18. Single nucleotide variants in theFrontiers in cellular and infection microbiology · 2024
    Observational
  19. Article
  20. 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

7 authors at 2 institutions in 3 countries.

Angela IshakDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA. Electronic address: angela.ishak.10@gmail.com.
Meghana MehendaleDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA.
Mousa M AlRawashdehDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA; European University Cyprus - School of Medicine, Nicosia, Cyprus.
Cristina SestacovschiDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA.
Medha SharathDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA; Bangalore Medical College and Research Institute, Bangalore, Karnataka, India.
Krunal PandavDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA.
Sima MarzbanDepartment of Research & Academic Affairs, Larkin Community Hospital, South Miami, Florida, USA.
Larkin Community Hospital · USEuropean University Cyprus · CY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOVID-19 is associated with several risk factors such as distinct ethnicities (genetic ancestry), races, sexes, age, pre-existing comorbidities, smoking, and genetics. The authors aim to evaluate the correlation between variability in the host genetics and the severity and susceptibility towards COVID-19 in this study.

methodsFollowing the PRISMA guidelines, we retrieved all the relevant articles published until September 15, 2021, from two online databases: PubMed and Scopus.

findingsHigh-risk HLA haplotypes, higher expression of ACE polymorphisms, and several genes of cellular proteases such as TMPRSS2, FURIN, TLL-1 increase the risk of susceptibility and severity of COVID-19. In addition, upregulation of several genes encoding for both innate and acquired immune systems proteins, mainly CCR5, IFNs, TLR, DPPs, and TNF, positively correlate with COVID-19 severity. However, reduced expression or polymorphisms in genes affecting TLR and IFNλ increase COVID-19 severity.

conclusionHigher expression, polymorphisms, mutations, and deletions of several genes are linked with the susceptibility, severity, and clinical outcomes of COVID-19. Early treatment and vaccination of individuals with genetic predisposition could help minimize the severity and mortality associated with COVID-19.

Indexed as

COVID-19Genetic Predisposition to DiseaseHaplotypesHumansPolymorphism, GeneticSARS-CoV-2COVID-19 severityGenetic SusceptibilityHost geneticsPolymorphismsSARS-CoV-2

Identifiers

PMID35714803
PMCPMC9195407
OpenAlexW4282835288

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.