Evidence map›Paper›PMID 37270678›Full record

ArticleAnnals of Saudi medicine

Demographic, clinical and genetic factors associated with COVID-19 disease susceptibility and mortality in a Kurdish population.

Shukur Wasman Smail, Esmaeil Babaei, Kawa Amin

Open access · diamondAbstract read
In one paragraph

Article in Annals of Saudi medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Frontiers in medicine · 2024
    Article
  7. Biology · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. 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

3 authors at 3 institutions in 3 countries.

Shukur Wasman SmailFrom the Department of Biology, College of Science, Salahaddin University-Erbil, Iraq.ORCID 0000-0001-8188-2540
Esmaeil BabaeiFrom the Department of Biology, School of Natural Sciences, University of Tabriz, Tabriz, Iran.
Kawa AminFrom the College of Medicine, University of Sulaimani, Sulaymaniyah, Iraq.
Hawler Medical University · IQSalahaddin University-Erbil · IQUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronavirus disease 2019 (COVID-19) is a devastating pandemic that causes disease with a variability in susceptibility and mortality based on variants of various clinical and demographic factors, including particular genes among populations.

objectivesDetermine associations of demographic, clinical, laboratory, and single nucleotide polymorphisms in the

designProspective cohort study SETTINGS: Various cities in the Kurdistan Region of Iraq. PATIENTS AND

methodsThis prospective cohort study compared laboratory markers (D-dimer, tumor necrosis factor-alpha [TNF-α], interferon-gamma [IFN-γ], C-reactive protein [CRP], lymphocyte and neutrophil counts) between COVID-19 patients and healthy controls. DNA was extracted from blood, and genotypes were done by Sanger sequencing.

main outcome measuresSingle nucleotide polymorphisms of the SAMPLE SIZE: 203 (153 COVID-19 patients, 50 health control subjects).

resultsForty-eight (31.4%) of the COVID-19 patients died. Age over 40 and comorbidities were risk factors for mortality, but the strongest associations were with serum IFN-γ, the neutrophil-to-lymphocyte ratio (NLR), and serum TNF-α. The AA genotype and A allele of

conclusionsAge older than 40, comorbidities, the NLR and particular genotypes for and the LIMITATIONS: Small sample size. CONFLICT OF INTEREST: None.

Indexed as

COVID-19Tumor Necrosis Factor-alphaAngiotensin-Converting Enzyme 2Case-Control StudiesDemographyGenetic MarkersGenetic Predisposition to DiseaseGenotypeHumansInterferon-gammaPolymorphism, Single NucleotideProspective StudiesAngiotensin-Converting Enzyme 2Genetic MarkersInterferon-gammaTumor Necrosis Factor-alpha

Identifiers

PMID37270678
PMCPMC10317494
OpenAlexW4379278628

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.