Evidence map›Paper›PMID 34545062›Full record

ReviewSignal transduction and targeted therapy2021

Human genetic basis of coronavirus disease 2019.

Hao Deng, Xue Yan, Lamei Yuan

Abstract readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Human genetic basis of severe or critical illness in COVID-19.Frontiers in cellular and infection microbiology · 2022
    Review
  19. The association ofEXCLI journal · 2022
    Review
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

3 authors.

Hao Deng *Health Management Center, the Third Xiangya Hospital, Central South University, Changsha, China. hdeng008@yahoo.com.ORCID http://orcid.org/0000-0003-3240-4352
Xue Yan *Health Management Center, the Third Xiangya Hospital, Central South University, Changsha, China.
Lamei YuanHealth Management Center, the Third Xiangya Hospital, Central South University, Changsha, China.

Funding

Hunan Provincial Science and Technology Department (Department of Science and Technology of Hunan Province) 2020SK3032
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in considerable morbidity and mortality worldwide. COVID-19 incidence, severity, and mortality rates differ greatly between populations, genders, ABO blood groups, human leukocyte antigen (HLA) genotypes, ethnic groups, and geographic backgrounds. This highly heterogeneous SARS-CoV-2 infection is multifactorial. Host genetic factors such as variants in the angiotensin-converting enzyme gene (ACE), the angiotensin-converting enzyme 2 gene (ACE2), the transmembrane protease serine 2 gene (TMPRSS2), along with HLA genotype, and ABO blood group help to explain individual susceptibility, severity, and outcomes of COVID-19. This review is focused on COVID-19 clinical and viral characteristics, pathogenesis, and genetic findings, with particular attention on genetic diversity and variants. The human genetic basis could provide scientific bases for disease prediction and targeted therapy to address the COVID-19 scourge.

Indexed as

ABO Blood-Group SystemAngiotensin-Converting Enzyme 2COVID-19EthnicityFemaleGenotypeHLA AntigensHumansMalePeptidyl-Dipeptidase ARisk FactorsSARS-CoV-2Serine EndopeptidasesABO Blood-Group SystemACE2 protein, humanACE protein, humanAngiotensin-Converting Enzyme 2HLA AntigensPeptidyl-Dipeptidase ASerine EndopeptidasesTMPRSS2 protein, human

Identifiers

PMID34545062
PMCPMC8450706

What Socratic 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 Socratic graph.